<i>ECH1</i>-Deficiency-Mediated Polyunsaturated Fatty Acid Accumulation Promotes Vascular Smooth Muscle Cell Ferroptosis and Chronic-Kidney-Disease-Associated Plaque Vulnerability

ECH1-Deficiency-Mediated Polyunsaturated Fatty Acid Accumulation Promotes Vascular Smooth Muscle Cell Ferroptosis and Chronic-Kidney-Disease-Associated Plaque Vulnerability

PDF

Xianjin Bi¹^,³, Jinrun Zhou¹, Liang Liu¹, Zijin Chen¹, Bo Liang¹, Shihua Tian¹, Jiachuan Xiong¹, Qigang Lan¹, Liangjing Lv¹, Yan Li¹, Tangli Xiao¹, Ting He¹, Jun Zhang¹, Ling Nie¹, Jinghong Zhao¹^,²^,^*

Research. Vol 9 Article ID 1411

Less

Research. Vol 9 Article ID 1411

• RESEARCH ARTICLE •

ECH1-Deficiency-Mediated Polyunsaturated Fatty Acid Accumulation Promotes Vascular Smooth Muscle Cell Ferroptosis and Chronic-Kidney-Disease-Associated Plaque Vulnerability

Full

Affiliations

¹Department of Nephrology, the Key Laboratory for the Prevention and Treatment of Chronic Kidney Disease of Chongqing, Chongqing Clinical Research Center of Kidney and Urology Diseases, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing 400037, China.

²Key Laboratory of Geriatric Cardiovascular and Cerebrovascular Disease Research (Army Medical University), Ministry of Education, Chongqing 400037, China.

³Department of Cardio-Renal Department, People’s Liberation Army Joint Logistic Support Force 945th Hospital, Ya’an 625000, China.

About Author:

^† These authors contributed equally to the work.

Published: 2026-09-20 doi: 10.34133/research.1411

Outline

Abstract

Less

Vulnerable atherosclerotic plaques represent a critical pathological basis of acute cardiocerebrovascular events. Previous studies indicate that atherosclerotic plaques are more vulnerable under chronic kidney disease (CKD) milieus. Emerging evidence highlights that vascular smooth muscle cells (VSMCs) play a pivotal role in maintaining plaque stability, but the underlying mechanisms remain incompletely elucidated. Here, single-cell sequencing and functional enrichment analysis of arterial tissues from patients with CKD are performed, identifying lipid metabolism disorders in VSMCs. Further utilizing spatial and targeted lipidomics, apolipoprotein-E-deficient (ApoE^−/−) mouse with CKD (CKD/ApoE^−/− mouse) and bioinformatics analysis, we investigate the lipidomic profile of VSMCs and find that VSMCs in CKD-associated vulnerable plaques exhibit significant accumulation of polyunsaturated fatty acids (PUFAs), which induces VSMC ferroptosis and exacerbates plaque vulnerability. Mechanistically, the deficiency of ECH1 leads to the accumulation of PUFA in VSMCs, thereby inducing ferroptosis in fibrous cap VSMCs and fibrous cap thinning. Meanwhile, low expression of mRNA binding protein human antigen R (HuR) resulting from CKD milieus mediates the lack of ECH1 in VSMCs. In contrast, VSMC-specific overexpression of ECH1, inhibition of PUFA release using giripladib or suppression of PUFA lipid peroxidation with PRGL493 significantly alleviate VSMC ferroptosis and CKD-associated plaque vulnerability. These findings reveal that ECH1-deficiency-driven PUFA accumulation is responsible for VSMC ferroptosis and atherosclerotic plaque vulnerability. Targeted regulation of ECH1-mediated PUFA metabolism may be a promising preventive and therapeutic strategy for CKD-associated plaque vulnerability.

Cite this Article

Xianjin Bi, Jinrun Zhou, Liang Liu, Zijin Chen, Bo Liang, Shihua Tian, Jiachuan Xiong, Qigang Lan, Liangjing Lv, Yan Li, Tangli Xiao, Ting He, Jun Zhang, Ling Nie, Jinghong Zhao. ECH1-Deficiency-Mediated Polyunsaturated Fatty Acid Accumulation Promotes Vascular Smooth Muscle Cell Ferroptosis and Chronic-Kidney-Disease-Associated Plaque Vulnerability[J]. Research, 2026 , 9 (9) : 1411 - . DOI: 10.34133/research.1411

Full Text

Less

Introduction

Less

Cardiocerebrovascular diseases are the leading cause of mortality worldwide, accounting for approximately 19.8 million deaths each year and nearly one-third of all deaths globally [1,2]. Vulnerable atherosclerotic plaques can trigger the formation of thrombus and subsequent cardiovascular and cerebrovascular events [3]. Recent study indicates that vulnerable plaques account for over 50% of cases in atherosclerotic disease [4]. Therefore, elucidating the mechanisms of vulnerable atherosclerotic plaques is crucial for identifying intervention targets in cardiocerebrovascular diseases.

Vulnerable atherosclerotic plaques are primarily characterized by a thin fibrous cap, a large necrotic core, and significant inflammatory cell infiltration [5,6]. Previous study confirms that the fibrous cap, mainly composed of vascular smooth muscle cells (VSMCs) and VSMC-produced matrix, is a primary determinant of plaque stability [7]. Fibrous cap VSMCs are the subset of VSMCs that reside within the fibrous cap structure of atherosclerotic plaques. They are predominantly derived from contractile VSMCs in the tunica media: Following phenotypic dedifferentiation, these medial VSMCs migrate across the internal elastic lamina into the intima and undergo local proliferation to accumulate in the fibrous cap region. Fibrous cap VSMCs serve as a critical atheroprotective cellular population that maintains the mechanical tensile strength of the plaque and protects against plaque rupture and subsequent atherothrombotic events. These cells predominantly exhibit a synthetic phenotype while retaining the expression of a subset of canonical contractile markers, such as actin alpha 2, smooth muscle (ACTA2) and transgelin (TAGLN) [8,9]. Typically, a reduction in the number of fibrous cap VSMCs aggravates fibrous cap thinning, thereby promoting plaque vulnerability and rupture [10]. Compared with patients without chronic kidney disease (CKD), patients with CKD exhibit more severe fibrous cap thinning. Our prior research demonstrates that VSMC senescence plays a pivotal role in the pathogenesis of plaque vulnerability [11]. However, inhibition of VSMC senescence only partially ameliorates atherosclerotic plaque vulnerability [11], indicating the involvement of additional mechanisms.

Lipid metabolism disorder is primarily related to progression of atherosclerosis and plaque stability [12,13]. Previous research has extensively investigated the role of VSMCs in lipid metabolism disorder and their contribution to atherosclerosis, with a particular focus on the mechanisms of formation of lipid-loaded VSMCs [14]. This process involves 4 core biological steps: the uptake of atherogenic lipoproteins by VSMCs, the intracellular esterification of cholesterol, hydrolysis of cholesteryl esters, and the efflux of cholesterol [15]. Based on this pathological mechanism, current treatment strategies primarily use statins and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors to reduce the amount of lipoprotein that can infiltrate the vessel wall and be engulfed by VSMCs [16,17]. However, despite intensive lipid-lowering therapy, the incidence of thrombotic events remains markedly high, often referred to as residual risk [18]. This clinical challenge indicates a limitation in current therapies that focus mainly on regulating the quantity of lipids. Therefore, precise characterization of the lipid profile of VSMCs within atherosclerotic plaques is essential for elucidating the mechanism of plaque vulnerability [14]. Nevertheless, the precise mechanisms driving lipid metabolism abnormalities in VSMCs and their role in plaque vulnerability remain incompletely understood.

In this study, we observed that fibrous cap VSMCs in CKD/ApoE^−/− mice displayed an accumulation of polyunsaturated fatty acids (PUFAs), which consequently induced VSMC ferroptosis and fibrous cap thinning. The deficiency of enoyl-coenzyme A hydratase 1 (ECH1) was confirmed as the prominent cause of PUFA accumulation in fibrous cap VSMCs. Regulating ECH1-mediated PUFA metabolism might be a critical avenue to inhibit VSMC ferroptosis and CKD-associated plaque vulnerability.

Results

Less

PUFA accumulation is observed in fibrous cap VSMCs of CKD/ApoE^−/− mice

To investigate the potential mechanism of VSMCs in CKD-associated plaque vulnerability, we conducted single-cell sequencing on arterial vascular tissues from patients with CKD (Fig. 1A). Gene Ontology (GO) functional enrichment analysis identified lipid metabolism disorders in VSMCs (Fig. 1B). The expression distributions of well-established lineage-specific marker genes across all annotated cell populations are presented as violin plots, verifying the accuracy of cell type annotation for human vascular single-cell RNA sequencing data (Fig. S1A). To address the lipidomic profile of VSMCs in CKD-associated plaque vulnerability, we performed the targeted lipidomics analysis, revealing a significant accumulation of PUFA and an obvious decrease in monounsaturated fatty acid (MUFA) in CKD-serum-cultured human VSMCs (hVSMCs) (Fig. 1C to E). Specifically, the levels of ferroptosis-associated PUFAs [19,20], including linoleic acid (LA; c18:2n6), linolenic acid (ALA; c18:3n3), and arachidonic acid (AA; c20:4n6), were significantly elevated (Fig. 1F to H) in hVSMCs. Consistently, the levels of AA, LA, and ALA were markedly increased in arterial VSMCs isolated from CKD/ApoE^−/− mice (Fig. 1I to K) and in mouse VSMCs treated with serum from CKD/ApoE^−/− mice (Fig. S1B to D). Spatial targeted lipidomic detection further confirmed the accumulation of PUFA in fibrous cap VSMCs in CKD/ApoE^−/− mice (Fig. 1L and M). These results indicated that the lipid profile of fibrous cap VSMCs in CKD-associated vulnerable plaques is characterized by the accumulation of PUFA.

PUFA accumulation promotes ferroptosis in fibrous cap VSMCs of CKD/ApoE^−/− mice

Based on single-cell sequencing analysis, the cumulative distribution function revealed a significant reduction in the ferroptosis suppressor score of VSMCs in patients with end-stage renal disease (ESRD), which is consistent with the accumulation of PUFA triggering ferroptosis (Fig. 2A and B). Accordingly, gene set enrichment analysis (GSEA) of our published single-VSMC microarray data (GSE135626) identified significant enrichment of ferroptosis-associated pathways in VSMCs under CKD milieus (Fig. 2C and D). In CKD/ApoE^−/− mice, accelerated atherosclerosis, fibrous cap thinning, reduced VSMC number, decreased intraplaque collagen content, and enlarged necrotic core area were observed, accompanied by significantly shortened vessel occlusion time in the ferric chloride (FeCl₃)-induced carotid thrombosis assay (Fig. S2A to E). We observed marked elevations in both malondialdehyde (MDA) (Fig. 2E) and reactive oxygen species (ROS) levels (Fig. 2F) in arteries and fibrous cap of CKD/ApoE^−/− mice. Meanwhile, 4-hydroxynonenal (4-HNE) expression was significantly increased in fibrous cap VSMCs of CKD/ApoE^−/− mice (Fig. 2G and H), accompanied by ferroptosis-associated morphological changes, including mitochondrial shrinkage, increased membrane density, and reduced or absent cristae (Fig. 2I). Moreover, the expression of glutathione peroxidase 4 (GPX4) and solute carrier family 7 member 11 (SLC7A11) were both significantly down-regulated in atherosclerotic vessels of CKD/ApoE^−/− mice (Fig. S2F to J). In vitro, CKD serum incubation induced ferroptosis-associated morphological alterations, the elevation of MDA, ROS, lipid ROS, and oxidized boron-dipyrromethene (BODIPY) fluorescence intensity, as well as decreased reduced glutathione (GSH)/oxidized glutathione (GSSG) ratio and down-regulated expression of GPX4 and SLC7A11 in hVSMCs and primary mouse VSMCs (Fig. 2J to M and Fig. S3A to L). In summary, these findings confirmed that PUFA accumulation in fibrous cap VSMCs under CKD milieus could induce lipid peroxidation and ferroptosis.

Given that cytosolic phospholipase A2 (cPLA2) is the major rate-limiting enzyme for releasing PUFA [21], we used a specific cPLA2 inhibitor, giripladib, to block PUFA accumulation [22]. Giripladib treatment ameliorated PUFA accumulation (Fig. S4A to C), reduced arterial MDA production, diminished 4-HNE expression, and mitigated mitochondrial-ferroptosis-associated morphological alterations in fibrous cap VSMCs within the atherosclerotic plaques of CKD mice (Fig. 3A to D). Furthermore, it significantly mitigated atherosclerotic plaque vulnerability (Fig. 3E to K and Fig. S4D and E). Consistent with these findings in vivo, pretreatment of hVSMCs with giripladib significantly attenuated CKD-serum-induced PUFA accumulation (Fig. S4F to H), inhibited the elevation of MDA, ROS, and lipid ROS levels, and restored the GSH/GSSG ratio in hVSMC (Fig. S4I to M). Overall, these data emphasize that PUFA accumulation promotes VSMC ferroptosis and CKD-associated atherosclerotic plaque vulnerability.

ECH1 deficiency contributes to PUFA accumulation and VSMC ferroptosis under CKD milieus

To investigate the underlying mechanisms of PUFA accumulation in VSMCs under CKD milieus, we integrated differentially expressed genes (DEGs) from previous microarray data (GSE135626), FerrDB databases [23], and genes implicated in PUFA metabolism by intersection analysis [24]. The results hinted that ECH1 might be instrumental in PUFA accumulation and VSMC ferroptosis (Fig. 4A). Accordingly, the expression of ECH1 was markedly decreased in arteries and fibrous cap VSMCs of CKD/ApoE^−/− mice and human vascular samples from patients with ESRD (Fig. 4B to D and Fig. S5A). In vitro, ECH1 expression was also decreased in hVSMCs after CKD serum treatment (Fig. 4E to G). Overexpression of ECH1 (Fig. S5B and C) in hVSMCs alleviated the accumulation of PUFAs and mitochondrial damage and suppressed the MDA, ROS, and lipid ROS levels, as well as the decreased ratio of GSH/GSSG, indicating a reduction in lipid peroxidation and ferroptosis (Fig. 4H to M and Fig. S5D to K).

ECH1 primarily metabolizes endogenous PUFAs. Meanwhile, exogenous AA, a prototypical ω-6 PUFA, is oxidized by lipoxygenase to induce ferroptosis [25]. Thus, we further investigated whether exogenous AA could independently or synergistically promote ferroptosis in CKD-serum-incubated hVSMCs to simulate clinical scenarios of excessive PUFA exposure. We found that AA treatment exacerbated the accumulation of AA, MDA, ROS, and lipid ROS levels, as well as the decreased ratio of GSH/GSSG in CKD-serum-incubated VSMCs (Fig. S6A to J). However, AA treatment alone did not affect lipid peroxidation in VSMCs (Fig. S6A to J). Moreover, ECH1 overexpression could reverse the exacerbating effect of AA on CKD-induced ferroptosis in VSMCs (Fig. S7A to E). Collectively, these results indicated that the down-regulation of ECH1 in VSMCs induced by CKD milieus is a major factor in promoting PUFA accumulation, which subsequently triggers lipid peroxidation and ferroptosis.

Human antigen R down-regulation induces ECH1 deficiency in VSMCs under CKD milieus

To elucidate the underlying mechanism of ECH1 deficiency, we detected the stability of ECH1 mRNA in hVSMCs after CKD serum treatment and found a significant reduction (Fig. 5A). GSEA of previous microarray data revealed enrichment in the “Regulation of mRNA stability by proteins that bind ARE” pathway (Fig. 5B) [26]. Database predictions and previous cross-linking and immunoprecipitation sequencing data identified that human antigen R (HuR) is the only adenine–uracil-rich element (ARE)-binding protein predicted protein to interact with ECH1 mRNA, and HuR binds to 6 motifs within the 3′-untranslated region (UTR) region of ECH1 mRNA (Fig. 5C). Moreover, a positive correlation was observed between ECH1 and HuR expression (http://utrdb.cloud.ba.infn.it/utrdb/). Notably, decreased HuR levels were observed in arteries of CKD/ApoE^−/− mice and human vascular samples from patients with ESRD (Fig. 5D and Fig. S8A) and CKD-serum-treated VSMCs in vitro (Fig. 5E). Subsequently, knocking down HuR using short interfering RNA in vitro (Fig. S8B and C) reduced the stability of ECH1 mRNA, thereby decreasing the expression of ECH1 (Fig. S8F and G). Overexpression of HuR (Fig. S6D and E) significantly mitigated CKD-induced ECH1 mRNA instability and enhanced ECH1 expression (Fig. 5F and G). Notably, RNA immunoprecipitation (RIP)-polymerase chain reaction (PCR) experiments confirmed a direct binding relationship between HuR and ECH1 mRNA (Fig. 5H). Furthermore, overexpression of HuR mitigated CKD-induced accumulation of PUFAs, attenuated the elevation of MDA levels, and prevented the decline of GSH-to-GSSG ratio (Fig. 5I to M). Therefore, the above data suggest that HuR down-regulation serves as a critical mechanism underlying ECH1 deficiency.

VSMC-specific ECH1 overexpression stabilizes atherosclerotic plaques by inhibiting ferroptosis in fibrous cap VSMCs

To further elucidate the role of ECH1 in vulnerable atherosclerotic plaque, we established a mouse model featuring a conditional site-specific knock-in of ECH1 at the Rosa26 locus [C57BL/6J-Gt(ROSA)26Sor^{em1(CAG-LSL-Kozak-ECH1-WPRE-pA)1Smoc}] (Fig. 6A and Table S1). Subsequently, this mouse strain was crossed with Tagln-Cre and ApoE^−/− mouse to generate ApoE^−/− mouse exhibiting VSMC-specific overexpression of ECH1 (ECH1^Tagln-OE-ApoE^−/−) (Fig. 6B and Fig. S9A to C). ECH1^R26-LSL-ApoE^−/− mice were applied as the control group. ECH1^Tagln-OE-ApoE^−/− and ECH1^R26-LSL-ApoE^−/− mice underwent either a sham operation or CKD surgery and were subsequently maintained on a high-fat diet for 12 weeks (Fig. 6B). Notably, VSMC-specific overexpression of ECH1 ameliorated PUFA accumulation, decreased the expression of 4-HNE and MDA, and suppressed mitochondrial damage in plaque fibrous cap VSMCs (Fig. 6C to K). Meanwhile, VSMC-specific overexpression of ECH1 markedly attenuated atherosclerosis progression and enhanced atherosclerotic plaque stability (Fig. 7A to E and Fig. S10A to D). In conclusion, these findings suggested that ECH1-deficiency-induced VSMC ferroptosis promotes plaque vulnerability and atherosclerosis progression in mice, especially in CKD/ApoE^−/− mice.

Inhibition of ACSL4 alleviates VSMC ferroptosis and atherosclerotic plaque vulnerability of CKD/ApoE^−/− mice

Previous studies have demonstrated that acyl-coenzyme A synthetase long-chain family member 4 (ACSL4) is a key enzyme in PUFA lipid peroxidation [27]. Thus, the pharmacological ACSL4 inhibitor PRGL493 was used to explore the role of PUFA metabolism in VSMC ferroptosis within vulnerable atherosclerotic plaques. PRGL493 treatment decreased the expression of 4-HNE in fibrous cap VSMCs and arteries (Fig. 8A to D), reduced arterial MDA production, and attenuated the characteristic features of ferroptosis in fibrous cap VSMCs in CKD/ApoE^−/− mice (Fig. 8E and F). Consistent with these findings in vivo, PRGL493 pretreatment significantly mitigated mitochondrial damage, reduced MDA, ROS, and lipid ROS levels, and restored the GSH/GSSG ratio in CKD-serum-incubated hVSMCs (Fig. S11D to K). Nonetheless, there was no significant impact of PRGL493 on PUFA levels (Fig. 8I to K and Fig. S11A to C). Furthermore, PRGL493 treatment markedly mitigated atherosclerosis progression and plaque vulnerability (Fig. 8G and H and Fig. S12A to D).

At last, as PRGL493 and ECH1 overexpression mitigated CKD-induced ferroptosis via distinct mechanisms, we further explored the potential synergistic inhibitory effects of combining PRGL493 with ECH1 overexpression. Combined treatment exhibited a significantly enhanced synergistic inhibitory effect on CKD-induced hVSMC ferroptosis and resulted in a marked reduction in ferroptosis-associated markers (including MDA, ROS, and lipid ROS levels in hVSMCs) (Fig. S13A to D), accompanied by a significant increase in GSH/GSSG ratio (Fig. S13E).

Discussion

Less

Recent studies have demonstrated that stable and vulnerable plaques exhibit distinct spatial distribution characteristics of lipids across different plaque regions, suggesting that investigating local lipid profile could provide a novel perspective for exploring molecular mechanisms of atherosclerosis progression [28]. However, research in this field currently relies predominantly on untargeted spatial metabolomics techniques [29,30], which have inherent limitations. Certain lipid molecules (such as PUFAs and MUFAs) are prone to degradation at plaque sites during detection [31], resulting in loss of critical lipid information. Notably, targeted spatial metabolomics studies specifically focusing on the fibrous cap region of atherosclerotic plaques remain unexplored. This study bridges this gap through integrated multidimensional approaches. First, single-cell analysis of vascular samples from patients with CKD revealed distinct lipid metabolic dysregulation signatures in VSMCs under CKD milieus. Subsequent in vitro targeted metabolomics validation confirmed that CKD induces significant accumulation of PUFAs in VSMCs. Finally, targeted spatial metabolomics techniques clarified that PUFAs specifically accumulate in the fibrous cap region of CKD-associated plaques. These findings provide pivotal molecular evidence for understanding the lipid metabolic mechanisms driving CKD-related plaque vulnerability.

The stability of atherosclerotic plaques is a critical factor influencing the prognosis in patients with cardiocerebrovascular diseases. VSMCs, as the principal structural component of the fibrous cap in atherosclerotic plaques, play an essential role in regulating atherosclerotic plaque stability [7]. Growing evidence indicates that VSMC ferroptosis is closely associated with multiple cardiovascular diseases [32], including vascular calcification [33], aortic dissection [34], abdominal aortic aneurysm [35], and atherosclerosis [36]. Notably, 2 studies have directly examined the impact of VSMC ferroptosis in plaque stability. One study finds that administration of ferroptosis inhibitor ferrostatin-1 (1.0 mg/kg) stabilizes atherosclerotic plaques in ApoE^−/− mice [37]. Nonetheless, this study uses a conventional model of atherosclerosis in ApoE^−/− mice. Another study established an atherosclerosis model in ApoE^−/− mice by subjecting them to partial ligation of the left common carotid artery, followed by 4 weeks of high-fat diet feeding [38]. This model is characterized by rapid progression and localized lesion formation [39]. In contrast to the model utilized in our study, it is noteworthy that CKD/ApoE^−/− mouse model approximates more closely the complex pathological context observed in humans, while the former model lacks the systemic metabolic disease background. The establishment and merits of CKD/ApoE^−/− mouse model have been comprehensively examined in our previously published work [11]. Thus, above evidence suggests that inhibiting VSMC ferroptosis may be a potential therapeutic approach for the treatment of atherosclerosis progression and vulnerable plaques.

Accumulating evidence indicates that ferroptosis contributes to the pathogenesis of multiple diseases [40,41]. Previous studies have explored the molecular mechanisms of VSMC ferroptosis in cardiovascular disease, focusing on factors such as GSH/GPX4 inhibition [42], iron metabolic dysfunction [34], oxidative stress [43], mitochondrial dysfunction [44], and epigenetic regulation [45]. While PUFA metabolism is recognized as a crucial mechanism in ferroptosis [46], its specific role and regulatory mechanism in VSMCs within atherosclerotic vulnerable plaque remain inadequately understood. Through spatial and targeted metabolomics and gas chromatography-mass spectrometry (GC-MS) detection, we examine long-chain fatty acid levels in VSMCs and discover that PUFA accumulation induces VSMC ferroptosis. Our findings underscore the pivotal role of PUFA metabolism. Previously, impaired catabolism and accumulation of PUFA have been identified as critical mediators of ferroptosis in prostate cancer cells [47]. Studies [48,49] have demonstrated that silencing 2,4-dienoyl-CoA reductase 1 (DECR1), a key gene involved in PUFA metabolism, disrupts normal PUFA metabolic processes. This disruption leads to the intracellular accumulation of PUFA, thereby triggering lipid peroxidation and ultimately promoting the onset of ferroptosis. Similarly, our findings reveal that PUFA metabolic dysfunction and accumulation constitute central mechanisms driving VSMC ferroptosis in vulnerable atherosclerotic plaque.

ECH1 is an enzyme predominantly localized within the mitochondria and facilitates the catabolism of PUFA as energy-producing fatty acid substrates [50]. Consequently, the expression and activity of ECH1 are critical for the rate and efficiency of PUFA β-oxidation [51]. Notably, endogenous ECH1 has been reported to suppress ferroptosis in liver cells [52]. However, the precise mechanism by which ECH1 inhibits ferroptosis remains inadequately explored. In this study, we discover the mechanism through which ECH1 suppresses ferroptosis induced by PUFA accumulation. Previous research has examined the effects of exogenous ECH1 on atherosclerotic plaques, revealing that supplementation with ECH1 recombinant protein (0.5 μg/ml) inhibited plaque formation in ApoE^−/− mice [53]. Nonetheless, this study did not investigate the impact of endogenous ECH1 in VSMCs on plaque stability. In our study, we further elucidate the role of endogenous ECH1. By developing a VSMC-specific ECH1 overexpression mouse model and overexpressing ECH1 in vitro, we demonstrate that overexpression of endogenous ECH1 inhibits VSMC ferroptosis and improves plaque stability.

HuR regulates posttranscriptional processes by binding to specific mRNA sequences, exerting central regulatory roles in tumorigenesis [54], inflammation, and vascular diseases [55]. Recent studies have revealed that HuR exhibits a dual functional mode in atherosclerosis progression [56]. It has been reported that HuR enhances C-FOS protein levels by stabilizing C-FOS mRNA, directly driving VSMC proliferation and migration, and promoting vascular remodeling and neointima hyperplasia, which is a key driving step in early atherosclerosis pathogenesis [57]. Liu et al. [58] confirmed that VSMC-specific knockout of HuR accelerates AMP-activated protein kinase catalytic subunit α1/α2 (AMPKα1/α2) mRNA degradation, induces autophagy deficiency, and exacerbates atherosclerotic instability. This aligns with our finding that HuR plays a protective role in maintaining plaque stability under CKD milieus. Vascular remodeling and neointima hyperplasia are early driving events in atherosclerosis [59], while in late-stage plaques, the main pathological characteristics shift to cell death, aging, and plaque vulnerability [9]. Thus, biological effects of HuR are determined by key mRNA targets and specific pathological microenvironments. Notably, we discover a novel interaction that HuR regulates ECH1 mRNA stability in VSMCs and emphasize that targeting HuR for disease intervention requires precise analysis of cell type specificity and pathological-environment-dependent functional networks.

Given the critical involvement of ferroptosis in VSMCs within atherosclerotic vulnerable plaque, we evaluate the translational potential of our study in treating vulnerable plaque using newly identified cPLA2 and ACSL4 inhibitors. Pharmacological inhibition of cPLA2 and ACSL4 inhibitors can mitigate the release of PUFA and correspondingly relieve PUFA lipid peroxidation. Previous studies have shown that traditional Chinese medicinal compounds with cPLA2 inhibitory activity, such as tanshinone I [60] and salidroside [61], can significantly decrease the risk of cardiovascular disease. Our findings indicate that giripladib, a specific cPLA2 inhibitor, [62] exerts a protective role on vulnerable atherosclerotic plaque. However, clinical trials of giripladib are terminated at phase II (clinicaltrials.gov) due to pronounced gastrointestinal side effects. Therefore, future research on cPLA2 inhibition for treating vulnerable plaques could focus on the active ingredients in traditional Chinese medicine and the structural modifications of giripladib. ACSL4 serves as a crucial enzyme in the process of PUFA lipid peroxidation [63]; research has shown that its activity can be inhibited through various pathways. Inhibition of ACSL4 with atorvastatin [64], berberine [65], or magnesium ions [66] could significantly retard the atherosclerotic progression. In addition, recent studies have identified PRGL493 as a highly efficient and selective inhibitor of ACSL4 [67]. However, the application of PRGL493 in atherosclerosis-related research has not yet been explored, we demonstrate that PRGL493 plays a protective role in vulnerable atherosclerotic plaque.

The limitation of this study is that we only characterized the accumulation of AA, LA, and ALA, while the profiles of ω-3 PUFAs (e.g., eicosapentaenoic acid, docosahexaenoic acid, and docosapentaenoic acid) were not systematically examined. The potential regulatory effects of ω-3 PUFAs on VSMC ferroptosis and atherosclerotic lesion progression deserve independent and thorough investigation in future work. Moreover, while we delineate the downstream ECH1/HuR regulatory axis underlying PUFA accumulation, the specific upstream pathogenic mediators in CKD serum that initiate this metabolic reprogramming remain to be definitively isolated and functionally validated.

In conclusion, our study demonstrates that ECH1 deficiency in fibrous cap VSMCs induced PUFA accumulation and enhanced lipid peroxidation, which promote VSMC ferroptosis and contribute to the vulnerability of atherosclerotic plaques. Mechanically, the decreased expression of ECH1 is mediated by the reduction of HuR. The application of giripladib, PRGL493, and overexpressing ECH1 may provide promising therapeutic strategies by targeting PUFA metabolism in VSMCs for treating atherosclerotic plaque vulnerability. Overall, our research elucidates novel mechanisms underlying atherosclerotic plaque vulnerability and suggests promising strategies for its prevention and treatment.

Materials and Methods

Less

Animals

ApoE^−/− mice (C57BL/6J background, male, 8 weeks old, weighing 20 to 25 g) were obtained from SJA Laboratory Animal Co. Ltd. C57BL/6J-Gt(ROSA)26Sor^{em1(CAG-LSL-Kozak-ECH1-WPRE-pA)1Smoc} (ECH1^R26-LSL) mice were generated using the CRISPR–Cas9 technique by the Shanghai Model Organisms Center. Specifically, the CRISPR–Cas9 technology was used to introduce a knock-in at the Rosa26 locus. This technology involves designing guide RNAs specific to the gene of interest, which direct the Cas9 nuclease to modify the genome at the insertion site. This process enhances the efficiency of homologous recombination within the targeted genomic region, facilitating the homologous recombination of the target fragment into the desired locus. The inserted coding DNA sequence has a full length of 984 bp, with the specific sequence detailed in Table S1. To generate ECH1^Tagln-OE-ApoE^−/− mice, ECH1^R26-LSL mice were crossed onto ApoE^−/− and Tagln-Cre mice. To compare plaque morphology, ECH1^R26-LSL-ApoE^−/− mice were utilized as control. A classic 2-step 5/6 nephrectomy was performed to establish the CKD mouse model, with the detailed and standardized surgical procedure fully validated and described in our previous study [11]. After the second surgery, high-fat diet (H10141, HFK Biologic Technology) was administered to the mice. For giripladib (MedChemExpress) or PRGL493 (MedChemExpress) treatment, mice were treated utilizing a dose of 7.5 or 0.25 mg/kg intraperitoneally every day. After 12 weeks on the high-fat diet, the mice were anesthetized and euthanized; blood, hearts, and arteries were collected for further analyses. The metabolic parameters of mice are listed in Tables S2 to S5. All mice were pathogen-free and maintained under specific-pathogen-free conditions. Experimental units were individual mice. All the experimental procedures were approved by the Animal Care Committee of the Army Medical University (AMUWEC20222973).

Single-cell RNA sequencing on 10x Genomics Chromium platform

Vascular tissues trimmed during surgery from 4 patients with ESRD scheduled for renal transplantation were collected as the disease group, while vascular tissues trimmed from 3 healthy donor kidneys were selected as the control group. Detailed baseline clinical characteristics of all enrolled subjects are summarized in Table S10. Subsequently, single-cell sample preparation of the vascular tissues was carried out, followed by cell counting and quality control to ensure that the samples contained an optimal concentration of viable cells. Based on the predetermined number of cells to be acquired, Gel Bead-in-Emulsions for single-cell separation were constructed. After the Gel Bead-in-Emulsions were normally formed, they were collected and placed in a PCR instrument for reverse transcription to achieve labeling. Then, cDNA amplification was performed, followed by the construction of a gene expression library. Ultimately, the library mixture was sequenced on an Illumina 10x Genomics Chromium sequencer using 150-bp paired-end reads. After quality control of the sequencing data, the remaining cells were normalized, and variable genes were identified. The Uniform Manifold Approximation and Projection (UMAP) method was used to visualize data in a 2-dimensional space. For cell type classification, the FindClusters function in Seurat was used for unsupervised clustering, which adopts a graph-based clustering approach. Based on the expression of marker genes, the resolved cell clusters were annotated as specific cell types. In addition, GO functional enrichment analysis and ferroptosis-associated gene set variation analysis were performed on the differential genes of VSMCs between control and CKD group. The study protocol was approved by the Ethics Committee of Xinqiao Hospital (2024-Research063-02).

Cell culture

hVSMCs were acquired from the American Type Culture Collection. The culture condition is the Dulbecco’s modified Eagle’s medium (DMEM; Gibco) supplemented with 10% fetal bovine serum (Gibco) at 37 °C with 5% CO₂. The modeling method for simulating the CKD internal environment in vitro using hVSMCs is the same as depicted above. We utilized hVSMCs from passages 2 to 5 for tests. Cells were cultured in DMEM containing 10% uremic serum or human normal serum. For drug administration, the following reagents were used before treating with human normal or uremic serum: 10 μM giripladib (MedChemExpress), 50 μM PRGL493 (MedChemExpress), and 2.5 μM AA (MedChemExpress).

Transmission electron microscopy

Mouse aortas and hVSMCs were collected and fixed in 2.5% glutaraldehyde. The specimens were sent to the Biomedical Analysis Center (Army Medical University) for transmission electron microscopy (TEM) ultrastructural analysis. Using a JEM-1400 transmission electron microscope (JEOL, Tokyo, Japan) to examine and photograph the sections.

GSH/GSSG assay

Based on the manufacturer’s procedures for the GSH/GSSG assay kit (Beyotime), intracellular GSH and GSSG levels were determined as follows. After treatment, hVSMCs were gathered, and the supernatant was removed. A protein removal reagent solution M was added, and the mixture was centrifuged at 10,000g for 10 min at 4 °C. Then, the supernatant was collected for analysis. The total glutathione content in each sample was determined by preparing a standard curve and measuring its absorbance at 412 nm. Subsequently, GSH in the samples was eliminated using a GSH-removing auxiliary solution, and absorbance at 412 nm was determined again to quantify GSSG levels. The GSH concentration was determined by subtracting the measured GSSG level from the total glutathione pool.

MDA assay

The relative MDA concentrations in arterial tissues and hVSMCs were assessed using an MDA assay kit (Beyotime) based on the protocols. Arterial tissues or cell samples were homogenized and lysed using an immunoprecipitation lysis buffer. The lysates were then centrifuged at 10,000g for 10 min, and supernatants were collected for subsequent assays. After sample preparation, protein concentrations were quantified. Standard solutions, test samples, and detection working solution were added separately into a 96-well plate. Measuring the absorbance of each sample was at 532 nm with a microplate reader.

Plaque and intracellular ROS analysis

To detect ROS production in plaques, fresh-frozen sections of the aortic root were incubated with 10 μM dihydroethidium (Thermo Fisher Scientific) dissolved in phosphate-buffered saline (PBS) at 37 °C for 0.5 h in the dark. The sections were immediately photographed utilizing a Zeiss LSM800 NLO confocal microscope (Carl Zeiss), and fluorescence intensity was quantified via ZEN software (Carl Zeiss).

Western blot analyses

Protein specimens isolated from hVSMCs or endothelium-removed aortas were used for Western blotting analysis, as previously described. Briefly, protein specimens were separated by SDS–polyacrylamide gel electrophoresis and transferred onto polyvinylidene difluoride membranes (Millipore). The membranes were blocked with 5% skimmed milk powder for 2 h at 37 °C and subsequently incubated overnight at 4 °C utilizing primary antibodies. Primary antibody against 4-HNE (ab48506; 1:1,000) was bought from Abcam (Cambridge, MA, UK). The primary antibodies against ECH1 (A12944; 1:1,000), HuR (A19622; 1:1,000), GPX4 (A27995; 1:1,000), SLC7A11(A25302; 1:1,000), and β-actin (AC026; 1:1,000) were obtained from Abclonal (Wuhan, China). β-Actin was used as loading control for normalization. Then, the membranes were incubated with secondary antibodies for 1 h, and signals were detected using a Bio-Rad ChemiDoc MP imager (Bio-Rad Laboratories, Hercules, CA, USA).

Quantitative PCR

RNA was extracted from endothelium-removed aortas and hVSMCs using TRIzol Plus reagent (TaKaRa) and reverse-transcribed into cDNA using PrimeScript RT Reagent Kit (TaKaRa). Quantitative PCR (qPCR) was performed on the CFX96 Real-Time System (Bio-Rad) using the GoTaq qPCR Master Mix (Promega) to determine the mRNA expression levels of the indicated genes. Data were normalized relative to β-actin. The primer sequences used are listed in Table S7.

Oil Red O staining

The intact aorta was meticulously dissected from the aortic root to the iliac bifurcation, with all perivascular adipose and connective tissues carefully removed. The vessel was then longitudinally incised along the lesser curvature of the aortic arch to expose the lumen, extending proximally to the common carotid and subclavian arteries and distally to the iliac arteries. The dissected aorta was fixed in 4% paraformaldehyde for 24 h and subsequently stained with a freshly prepared Oil Red O working solution (Solarbio) at 37 °C for 60 min. Nonspecific background staining was differentiated by briefly rinsing the samples with 60% isopropanol. Quantitative analysis of the atherosclerotic lesion areas was conducted using ImageJ software.

Histology analysis of atherosclerotic plaque

We analyzed atherosclerotic plaque morphology and composition as depicted above. Briefly, mouse hearts were perfused and fixed in 4% paraformaldehyde for 24 h before sectioning. The aortic roots were embedded in paraffin and serially sectioned at a thickness of 4 μm through the region of the aortic valves. Aortic root paraffin sections were stained with hematoxylin and eosin (H&E) (for plaque and necrotic core area analysis) and Masson’s trichrome (for collagen content quantification) following standard procedures and subjected to immunohistological staining using an anti-α-smooth muscle actin (α-SMA; Abcam). The stained tissues and sections were imaged utilizing a microscope (Olympus Optical), and quantitative analyses were performed using ImagePro software.

FeCl₃-induced carotid artery thrombosis model

Carotid arterial thrombosis was induced using the FeCl₃ injury approach with minor modifications. Following adequate anesthesia, a midline cervical incision was made to carefully blunt-dissect and expose the common carotid artery. A perivascular miniature Doppler flow probe (Transonic Systems Inc.) was secured around the isolated vessel to continuously record real-time blood flow dynamics. To induce standardized endothelial injury, a 2 mm × 2 mm piece of Whatman filter paper presoaked with 10% FeCl₃ solution was topically applied to the adventitial surface of the carotid artery for 60 s. After removal of the filter paper, the injured segment was thoroughly rinsed with prewarmed (37 °C) sterile saline, and blood flow was monitored continuously for a total of 30 min. Time to complete vessel occlusion was defined as the interval from FeCl₃ application to persistent blood flow arrest lasting more than 30 s; specimens that did not develop full occlusion within the observation window were assigned a cutoff value of 30 min.

Immunofluorescence

For immunofluorescence (IF) staining, paraffin sections were prepared as described above. Antigen retrieval was performed by boiling the sections in citrate buffer (Santa Cruz Biotechnology) at over 95 °C for 0.5 h for sections. Subsequently, the sections were blocked utilizing goat serum (Beyotime) for 30 min at room temperature. The sections were then incubated overnight at 4°C with primary antibodies against 4-HNE (Abcam), ECH1 (Abclonal), HuR (Abclonal), or α-SMA (Abcam). After incubation, appropriate fluorescent-dye-conjugated secondary antibodies were used and using 4′,6-diamidino-2-phenylindole (DAPI; Beyotime) to counterstain. Finally, sections were photographed using a Zeiss LSM800 NLO confocal microscope (Carl Zeiss).

Ferroptosis assay

For the assessment of ferroptosis, fluorescent probes including 2′,7′-dichlorodihydrofluorescein diacetate (H₂DCFDA) and Liperfluo were used to measure ROS and lipid peroxide levels in hVSMCs. Probe loading was performed either in situ or after cell collection, followed by confocal fluorescence microscopy imaging and flow cytometric analysis of the aforementioned indicators. To visualize the staining of the fluorescent probes, hVSMCs were incubated with 1 μM 2′,7′-dichlorodihydrofluorescein diacetate (MedChemExpress), 5 μM BODIPY 581/591 C11 (Beyotime), or 5 μM Liperfluo (Dojindo Molecular Technologies) at 37 °C for 30 min in the dark after treatment. Subsequently, hVSMCs were rinsed with PBS to remove extra probes and photographed using a Zeiss LSM800 NLO confocal microscope (Carl Zeiss). For flow cytometry analysis, cells were first digested with trypsin and then incubated with the fluorescent probes and under the same incubation conditions mentioned above. Following washing with PBS to remove unbound probes, the hVSMCs were analyzed by flow cytometry.

Spatial targeted lipidomics

Spatial lipidomics enables the mapping of lipidomics distributions within aortic root plaque sections. Here, we present a targeted spatial metabolomics workflow that integrates on-tissue MS/MS fragmentation with authentic standard comparison for confident metabolite annotation. After pretreating the samples, which were stored at −80 °C, at 20 °C for 1 h, 10-μm sections were cut using a Leica CM1950 cryostat and immediately mounted onto indium-tin-oxide-coated slides (Bruker) for matrix-assisted laser desorption/ionization MS imaging; adjacent sections were stained with H&E. The slides were then vacuum-dried for 15 min, sealed, and stored at −80°C. A 1.5-mM 1,5-diaminonaphthalene solution (90% methanol/0.3% trifluoroacetic acid) was sprayed in 10 cycles using a TM-Sprayer (HTX Technologies) at the following parameters: speed, 1,200 mm/min; spacing, 3 mm; flow rate, 0.08 ml/min; temperature, 60 °C; nitrogen pressure, 10 psi. Images were acquired in negative ion mode using a Bruker thermal ionization mass spectrometry time-of-flight flex matrix-assisted laser desorption/ionization 2 with a 10-kHz SmartBeam 3-dimensional laser (range, 50 to 1,300 mass/charge ratio; pixel size, 10 μm × 10 μm; laser frequency, 10 kHz; energy, 70%; 200 repetitions per pixel). The data and ion imaging were processed using SCiLS Lab 2024b Pro. For targeted analysis, we prepared 3 standard samples in this experiment; details refer to the Table S8. Precursor ions of interest were selected on the basis of accurate mass (<3 parts per million), and on-tissue MS/MS spectra were acquired using collision energy ramping from 10 to 40eV to generate rich fragmentation patterns. Authentic standards were spotted onto metal target plate or the same tissue section at defined coordinates and analyzed under identical parameters. Identification was confirmed by matching MS/MS spectral similarity. Results refer to the Fig. S14. This targeted spatial metabolomics approach provides a robust framework for confident metabolite identification by combining the strengths of targeted acquisition (sensitivity, specificity) with orthogonal confirmation via standard comparison and MS/MS library matching. In general, if the matching score value is greater than 0.6, it is considered that the substance can be further qualitatively identified. The workflow is applicable to diverse tissue types and can be extended to isotope tracing and absolute quantification studies.

Lipidomics

The long-chain fatty acid content of hVSMCs and mouse aortic VSMCs was determined using targeted lipidomics combined with GC-MS. To correct for lipid extraction efficiency and sample processing losses, a deuterated internal standard (nonadecanoic acid-d37, 10 μg/ml) was added immediately at the initiation of lipid extraction (prior to organic solvent addition). All procedures were performed on ice with rapid processing to minimize phospholipid degradation and prevent artificial release of PUFAs from storage lipids. Samples were gradually thawed at 4 °C, and aliquots were transferred to 5 ml of ice-cold dichloromethane-methanol (2:1, v/v), followed by vigorous vortexing. The mixture was washed with 2 ml of ice-cold Milli-Q water, and the lower organic layer was collected and dried under a gentle nitrogen stream. The residue was redissolved in 2 ml of n-hexane, and acid-catalyzed methylation was performed for 0.5 h to derivatize long-chain fatty acids into fatty acid methyl esters, which enables efficient ionization and accurate GC-MS detection. After adding 2 ml of Milli-Q water, 2 ml of the supernatant was collected, dried under nitrogen, redissolved in n-hexane, and transferred to an injection vial (injection volume, 1 μl; split ratio, 10:1). Chromatographic separation was performed using an Agilent 19091S-433UI capillary column (HP-5ms; 30 m × 250 μm × 0.25 μm). A quality control sample (pooled sample mix) was included in each analytical batch to monitor system stability and reproducibility (Fig. S15). MS was performed using an Agilent 5977B mass-selective detector (MSD) with the following parameters: injection port, 280 °C; ion source, 230 °C; transfer line, 250 °C; electron ionization energy, 70 eV; and SCAN mode/selected-ion-monitoring (SIM) mode detection. Peak areas and retention times were extracted using MSD ChemStation, and quantification was performed using a 7-point standard curve calibrated with the internal standard to account for matrix effects and extraction recovery.

Primary cells isolation and culture

The aortas were carefully dissected from mice, followed by the manual removal of endothelial cells. The endothelium-denuded aortas from 5 mice were then pooled and cut into small pieces, each approximately 1 mm in dimension. To prepare a single-cell suspension, a mixed enzyme digestion solution was utilized containing collagenase I (450 U/ml), collagenase XI (250 U/ml), and hyaluronidase (120 U/ml; all from Sigma-Aldrich), along with deoxyribonuclease I (120 U/ml) obtained from Roche in Indianapolis, IN, USA. The digestion was carried out at 37 °C for a duration of 90 min. The resulting primary mouse VSMC single-cell suspension was then filtered through a 70-μm cell strainer. Subsequently, the cells were cultured in a 24-well plate using DMEM (Gibco) supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin/streptomycin.

Cell transfection

hVSMCs underwent transfection with plasmids overexpressing ECH1 or HuR (Youbio) or with ECH1/HuR-specific small interfering RNAs (Table S9) using Lipofectamine 3000 (Invitrogen), following established protocols. Transfection duration was 48 h. The small interfering RNAs, synthesized by MiaoLingPlasmid (Hubei), were validated for knockdown efficiency via quantitative reverse transcription PCR and Western blotting, using β-actin as an internal control.

RNA immunoprecipitation

RIP assays were conducted using a Millipore kit (Burlington) based on the manufacturer’s protocols. hVSMCs were lysed in 150 μl of RIP buffer, followed by 6-h incubation with 5 μg of anti-human immunoglobulin G (IgG) conjugated with magnetic beads or HuR antibodies (Abclonal). RNA–protein complexes were digested with proteinase K to isolate RNA, and HuR–ECH1 mRNA interactions were quantified by qPCR.

Statistical analysis

Data were analyzed using GraphPad Prism 10. Results are expressed as means ± SD, with n indicating mouse numbers or experimental replicates (see figure legends). When the data fit a normal distribution (normality was assessed using the Shapiro–Wilk test), 2-group comparisons used 2-tailed Student’s t tests, multigroup comparisons were conducted using analysis of variance (ANOVA), followed by post-hoc Tukey’s honestly significant difference tests. Statistical significance was defined as P < 0.05.

Ethical Approval

Less

All the experimental procedures were approved by the Animal Care Committee of the Army Medical University (AMUWEC20222973) and the Ethics Committee of Xinqiao Hospital (2024-Research063-02).

References

Less

GBD 2019 Stroke Collaborators. Global, regional, and national burden of stroke and its risk factors, 1990-2019: A systematic analysis for the global burden of disease study 2019. Lancet Neurol. 2021;20(10):795–820.

Vaduganathan

, Mensah

, Turco

, Fuster

, Roth

.The global burden of cardiovascular diseases and risk: A compass for future health. J Am Coll Cardiol. 2022;80(25):2361–2371.

Zhang

, Liu

, Cao

, Zhang

, Sun

, Wang

, Song

, Zhang

.Targeting the microenvironment of vulnerable atherosclerotic plaques: An emerging diagnosis and therapy strategy for atherosclerosis. Adv Mater. 2022;34(29):Article e2110660.

Covani

, Niccoli

, Fujimoto

, Scalamera

, Vergallo

, Porto

, McNulty

, Lee

, Kakuta

, Jang

.Plaque vulnerability and cardiovascular risk factor burden in acute coronary syndrome: An optical coherence tomography analysis. J Am Coll Cardiol. 2025;86(2):77–89.

Sun

, Singh

, Shami

, Kluza

, Pan

, Djordjevic

, Michaelsen

, Kennbäck

, van der Wel

, Orho-Melander

, et al.Spatial transcriptional mapping reveals site-specific pathways underlying human atherosclerotic plaque rupture. J Am Coll Cardiol. 2023;81(23):2213–2227.

Bentzon

, Otsuka

, Virmani

, Falk

.Mechanisms of plaque formation and rupture. Circ Res. 2014;114(12):1852–1866.

Basatemur

, Jørgensen

, Clarke

MCH

, Bennett

, Mallat

.Vascular smooth muscle cells in atherosclerosis. Nat Rev Cardiol. 2019;16(12):727–744.

Bennett

, Sinha

, Owens

.Vascular smooth muscle cells in atherosclerosis. Circ Res. 2016;118(4):692–702.

Grootaert

MOJ

, Bennett

.Vascular smooth muscle cells in atherosclerosis: Time for a re-assessment. Cardiovasc Res. 2021;117(11):2326–2339.

10.

Gaba

, Gersh

, Muller

, Narula

, Stone

.Evolving concepts of the vulnerable atherosclerotic plaque and the vulnerable patient: Implications for patient care and future research. Nat Rev Cardiol. 2023;20(3):181–196.

11.

, Du

, Wang

, Han

, Wang

, Qiao

, Zhu

, Ran

, Liu

, et al.Mitochondrial damage-induced innate immune activation in vascular smooth muscle cells promotes chronic kidney disease-associated plaque vulnerability. Adv Sci. 2021;8(5):Article 2002738.

12.

Ahn

, Burnett

, Wojnar-Lason

, Doja

, Sreekumar

, Ghoshal

, Singla

, Gonsalvez

, Harris

, Wang

, et al.Activation of receptor-independent fluid-phase pinocytosis promotes foamy monocyte formation in atherosclerotic mice. Redox Biol. 2024;78:Article 103423.

13.

Wang

, Chen

, Zhang

, Akhmedov

, Weng

, Xu

.Prioritization of lipid metabolism targets for the diagnosis and treatment of cardiovascular diseases. Research. 2025;8:Article 0618.

14.

Jinson

, Zhang

, Lancaster

, Murphy

, Morgan

.Iron, lipid peroxidation and ferroptosis play pathogenic roles in atherosclerosis. Cardiovasc Res. 2025;121(1):44–61.

15.

Liu

, Yuan

, Wu

, Hu

.Lipid accumulation and novel insight into vascular smooth muscle cells in atherosclerosis. J Mol Med. 2021;99(11):1511–1526.

16.

Mahmoudi

, Gorenne

, Mercer

, Figg

, Littlewood

, Bennett

.Statins use a novel Nijmegen breakage syndrome-1-dependent pathway to accelerate DNA repair in vascular smooth muscle cells. Circ Res. 2008;103(7):717–725.

17.

Cui

, Chen

, Li

, Zhang

, Wang

, Xia

, Gan

, Zhou

, Li

, Zhang

, et al.PCSK9 promotes atherosclerotic plaque instability by inducing VSMC ferroptosis through the YAP1-NUPR1 axis. Research. 2025;8:Article 0922.

18.

Ridker

, Bhatt

, Pradhan

, Glynn

, MacFadyen

, Nissen

.Inflammation and cholesterol as predictors of cardiovascular events among patients receiving statin therapy: A collaborative analysis of three randomised trials. Lancet. 2023;401(10384):1293–1301.

19.

Lee

, Nam

, Son

, Hyun

, Jang

, Kim

, Jung

, Jang

, Yoon

, et al.Polyunsaturated fatty acid biosynthesis pathway determines ferroptosis sensitivity in gastric cancer. Proc Natl Acad Sci USA. 2020;117(51):32433–32442.

20.

Wang

, Zhang

, Ren

, Qi

, Xie

, Shang

, Liu

.Dysregulated palmitic acid metabolism promotes the formation of renal calcium-oxalate stones through ferroptosis induced by polyunsaturated fatty acids/phosphatidic acid. Cell Mol Life Sci. 2024;81(1):85.

21.

Chao

, Gutiérrez-Vázquez

, Rothhammer

, Mayo

, Wheeler

, Tjon

, Zandee

SEJ

, Blain

, de Lima

, Takenaka

, et al.Metabolic control of astrocyte pathogenic activity via cPLA2-MAVS. Cell. 2019;179(7):1483–1498.e1422.

22.

Thotala

, Craft

, Ferraro

, Kotipatruni

, Bhave

, Jaboin

, Hallahan

.Cytosolic phospholipase A2 inhibition with PLA-695 radiosensitizes tumors in lung cancer animal models. PLOS ONE. 2013;8(7):Article e69688.

23.

Zhou

, Yuan

, Du

, Zhang

, Shi

, Bao

, Ning

, Peng

.FerrDb V2: Update of the manually curated database of ferroptosis regulators and ferroptosis-disease associations. Nucleic Acids Res. 2023;51(D1):D571–d582.

24.

Guryleva

, Penzar

, Chistyakov

, Mironov

, Favorov

, Sergeeva

.Investigation of the role of PUFA metabolism in breast cancer using a rank-based random Forest algorithm. Cancer. 2022;14(19):Article 4663.

25.

Kagan

, Mao

, Qu

, Angeli

, Doll

, Croix

, Dar

, Liu

, Tyurin

, Ritov

, et al.Oxidized arachidonic and adrenic PEs navigate cells to ferroptosis. Nat Chem Biol. 2017;13(1):81–90.

26.

, Deng

, Chen

.RNA-binding proteins in regulating mRNA stability and translation: Roles and mechanisms in cancer. Semin Cancer Biol. 2022;86(Pt 2):664–677.

27.

Zhou

, Zhao

, Lv

, Xu

, Liu

, Li

, Gao

, Zhao

, Zhang

, Li

, et al.ACSL4 promotes microglia-mediated neuroinflammation by regulating lipid metabolism and VGLL4 expression. Brain Behav Immun. 2023;109:331–343.

28.

Greco

, Bertagna

, Quercioli

, Pucci

, Rocchiccioli

, Ferrari

, Recchia

, McDonnell

.Lipids associated with atherosclerotic plaque instability revealed by mass spectrometry imaging of human carotid arteries. Atherosclerosis. 2024;397:Article 118555.

29.

Ntshangase

, Khan

, Bezuidenhout

, Gazárková

, Kaczynski

, Sellers

, Rattray

, Newby

, Hadoke

, Andrew

.Spatial lipidomic profiles of atherosclerotic plaques: A mass spectrometry imaging study. Talanta. 2024;282:Article 126954.

30.

Cao

, Martin-Lorenzo

, van Kuijk

, Wieland

, Gijbels

, Claes

BSR

, Heredero

, Aldamiz-Echevarria

, Heeren

RMA

, Goossens

, et al.Spatial metabolomics identifies LPC(18:0) and LPA(18:1) in advanced atheroma with translation to plasma for cardiovascular risk estimation. Arterioscler Thromb Vasc Biol. 2024;44(3):741–754.

31.

Morgan

, Pernes

, Huynh

, Giles

, Paul

, Smith

AAT

, Mellett

, Liang

, van Buuren-Milne

, Veiga

, et al.A lipid atlas of human and mouse immune cells provides insights into ferroptosis susceptibility. Nat Cell Biol. 2024;26(4):645–659.

32.

Yang

, Nawabi

, Yao

, Liu

.Ferroptosis of smooth muscle cells in vascular diseases: From basic principles to clinical translation. Cell Death Discov. 2026;12(1):140.

33.

Chen

, Sun

, Li

, Liu

.Oleoylethanolamide alleviates hyperlipidaemia-mediated vascular calcification via attenuating mitochondrial DNA stress triggered autophagy-dependent ferroptosis by activating PPARα. Biochem Pharmacol. 2023;208:Article 115379.

34.

Shi

, Wang

, Wei

, Huo

, Ye

, Yi

, Feng

, Fang

, Jiang

, Ma

.Histone acetyltransferase P300 deficiency promotes ferroptosis of vascular smooth muscle cells by activating the HIF-1α/HMOX1 axis. Mol Med. 2023;29(1):91.

35.

, Chen

, Lu

, Liu

, Lu

, Jiang

, Weng

.HMGB2 deficiency mitigates abdominal aortic aneurysm by suppressing Ang-II-caused ferroptosis and inflammation via NF-κβ pathway. Mediat Inflamm. 2023;2023(1):2157355.

36.

, Zhang

, Pan

, Zhao

, Zhang

.HSPB1 suppresses oxLDL-induced vascular smooth muscle cell ferroptosis by inhibiting DPP4. Arch Biochem Biophys. 2025;768:Article 110400.

37.

Chen

, Cui

, Li

, Xia

, Xiang

, Mao

, Li

, Chen

, Zeng

, Zheng

, et al.A novel mechanism of ferroptosis inhibition-enhanced atherosclerotic plaque stability: YAP1 suppresses vascular smooth muscle cell ferroptosis through GLS1. FASEB J. 2024;38(15):Article e23850.

38.

Guo

, Xie

, Yuan

, Liao

, Zheng

.Catechin inhibits ox-LDL-induced ferroptosis in vascular smooth muscle cells to alleviate and stabilize atherosclerosis. Front Nutr. 2025;12:1594708.

39.

Merino

, Parthasarathy

, Singla

.Partial ligation-induced carotid artery occlusion induces leukocyte recruitment and lipid accumulation—A shear stress model of atherosclerosis. Mol Cell Biochem. 2013;372(1-2):267–273.

40.

, Gao

, Zhuang

, Wang

, Wu

, Zhou

, Xie

, Zhao

, et al.Inhibition of ALOX12-12-HETE alleviates lung ischemia-reperfusion injury by reducing endothelial ferroptosis-mediated neutrophil extracellular trap formation. Research. 2024;7:Article 0473.

41.

Liu

, Zheng

, Yu

, Wang

, Yuan

, Shao

, Yang

, Shen

, Wang

, Li

, et al.Stimuli-responsive CuFeTe₂ nanosheets for amplified cuproptosis/ferroptosis in triple-negative breast cancer therapy. Adv Sci. 2025;13(3):Article e05739.

42.

, Chen

, Li

, Liang

, Wang

, Dong

, Fu

, Lan

, Li

, Liu

, et al.Repression of the antiporter SLC7A11/glutathione/glutathione peroxidase 4 axis drives ferroptosis of vascular smooth muscle cells to facilitate vascular calcification. Kidney Int. 2022;102(6):1259–1275.

43.

Song

, Chen

, Qin

, Xu

, Sun

, Zhong

, Lu

, Hu

, Wei

, Chen

.Oxidative stress drives vascular smooth muscle cell damage in acute Stanford type A aortic dissection through HIF-1α/HO-1 mediated ferroptosis. Heliyon. 2023;9(12):Article e22857.

44.

, Ye

, Chen

, Feng

, Huang

, Liang

, Lan

, Dong

, Liu

, Li

, et al.Oxidized phospholipid POVPC contributes to vascular calcification by triggering ferroptosis of vascular smooth muscle cells. FASEB J. 2024;38(7):Article e23592.

45.

Liao

, Zou

, Wu

, Bai

, Liu

, Zhi

, Qu

.METTL3-mediated m6A modification of NORAD inhibits the ferroptosis of vascular smooth muscle cells to attenuate the aortic dissection progression in an YTHDF2-dependent manner. Mol Cell Biochem. 2024;479(12):3471–3487.

46.

Wang

, Chen

, Yao

, Sun

, Wei

, Sun

, Zhang

, Li

, Butcher

, Sun

, et al.Lipid metabolism drives dietary effects on T cell ferroptosis and immunity. Nature. 2026;653(8113):200–211.

47.

Yang

, Kim

, Gaschler

, Patel

, Shchepinov

, Stockwell

.Peroxidation of polyunsaturated fatty acids by lipoxygenases drives ferroptosis. Proc Natl Acad Sci USA. 2016;113(34):E4966–E4975.

48.

Nassar

, Mah

, Dehairs

, Burvenich

, Irani

, Centenera

, Helm

, Shrestha

, Moldovan

, Don

, et al.Human DECR1 is an androgen-repressed survival factor that regulates PUFA oxidation to protect prostate tumor cells from ferroptosis. Elife. 2020;9:Article e54166.

49.

Blomme

, Ford

, Mui

, Patel

, Ntala

, Jamieson

, Planque

, McGregor

, Peixoto

, Hervouet

, et al.2,4-dienoyl-CoA reductase regulates lipid homeostasis in treatment-resistant prostate cancer. Nat Commun. 2020;11(1):2508.

50.

Keane

, Takahashi

, Dhayal

, Morgan

, Curi

, Newsholme

.Arachidonic acid actions on functional integrity and attenuation of the negative effects of palmitic acid in a clonal pancreatic β-cell line. Clin Sci. 2011;120(5):195–206.

51.

Shoukry

, Schulz

.Significance of the reductase-dependent pathway for the beta-oxidation of unsaturated fatty acids with odd-numbered double bonds. Mitochondrial metabolism of 2-trans-5-cis-octadienoyl-CoA. J Biol Chem. 1998;273(12):6892–6899.

52.

Liu

, Yi

, Mao

, Yang

, Rao

.Enoyl coenzyme a hydratase 1 alleviates nonalcoholic steatohepatitis in mice by suppressing hepatic ferroptosis. Am J Physiol Endocrinol Metab. 2021;320(5):E925–e937.

53.

Rao

, Qin

, Du

.ECH 1 attenuates atherosclerosis by reducing macrophage infiltration and improving plaque stability through CD36 degradation. Arch Biochem Biophys. 2024;763:Article 110217.

54.

Finan

, Sutton

, Dixon

, Brody

.Targeting the RNA-binding protein HuR in cancer. Cancer Res. 2023;83(21):3507–3516.

55.

Liu

, Jiang

, Lu

, Xing

, Qiao

, Zhang

.HuR (human antigen R) regulates the contraction of vascular smooth muscle and maintains blood pressure. Arterioscler Thromb Vasc Biol. 2020;40(4):943–957.

56.

Wang

, Zheng

, Zhou

, Xie

, Ren

, Liu

, Zhou

, Jiang

.Multifaceted nature of HuR in atherosclerosis development. Curr Med Chem. 2025;32(17):3423–3437.

57.

Wang

, Yang

, Zhao

, Wang

, Gong

, Zheng

, Liu

, Yang

, Lin

, et al.A novel hidden protein p-414aa encoded by circSETD2(14,15) inhibits vascular remodeling. Circulation. 2025;151(22):1568–1582.

58.

Liu

, Jiang

, Cui

, Wang

, Liu

, Li

, Yang

, Zhang

.Smooth muscle-specific HuR knockout induces defective autophagy and atherosclerosis. Cell Death Dis. 2021;12(4):385.

59.

, Mao

, Chen

, Yang

, Qiu

, Yu

, Jia

, Wu

, Wang

, et al.Peptide vaccine against ADAMTS-7 ameliorates atherosclerosis and postinjury neointima hyperplasia. Circulation. 2023;147(9):728–742.

60.

Kim

, Moon

, Chang

, Son

, Kang

, Kim

.Effects of tanshinone I isolated from salvia miltiorrhiza bunge on arachidonic acid metabolism and in vivo inflammatory responses. Phytother Res. 2002;16(7):616–620.

61.

Huang

, Yong

, Li

, Wen

, Zhou

, Liao

, You

, Yu

, Xu

, Wang

, et al.15-Lipoxygenase-2 deficiency induces foam cell formation that can be restored by salidroside through the inhibition of arachidonic acid effects. Open Life Sci. 2025;20(1):20251091.

62.

Duvernay

, Matafonov

, Lindsley

, Hamm

.Platelet Lipidomic profiling: Novel insight into cytosolic phospholipase A2α activity and its role in human platelet activation. Biochemistry. 2015;54(36):5578–5588.

63.

Liao

, Wang

, Kryczek

, Li

, Bian

, Sell

, Wei

, Grove

, Johnson

, et al.CD8⁺ T cells and fatty acids orchestrate tumor ferroptosis and immunity via ACSL4. Cancer Cell. 2022;40(4):365–378.e366.

64.

Tan

, Liu

, Qi

, Zhang

, Zhi

, Li

, Zhang

, Liu

.Atorvastatin attenuates endothelial cell injury in atherosclerosis through inhibiting ACSL4-mediated Ferroptosis. Cardiovasc Ther. 2024;2024(1):5522013.

65.

Hong

, Feng

, Dou

, Sun

, Hu

, Chen

, Liu

, Xu

, Du

, Tang

, et al.Berberine as a novel ACSL4 inhibitor to suppress endothelial ferroptosis and atherosclerosis. Biomed Pharmacother. 2024;177:Article 117081.

66.

, Zhou

, Yang

, Yu

, Zhang

, Liang

, Tan

, Song

, Wang

, Sun

, et al.Mitigation of arteriosclerosis through transcriptional regulation of ferroptosis and lipid metabolism by magnesium. Biomaterials. 2025;319:Article 123135.

67.

Castillo

, Orlando

, Maloberti

, Prada

, Dattilo

, Solano

, Bigi

, Ríos Medrano

, Torres

, Indo

, et al.New inhibitor targeting acyl-CoA synthetase 4 reduces breast and prostate tumor growth, therapeutic resistance and steroidogenesis. Cell Mole Life Sci. 2021;78(6):2893–2910.

Appendix

Less

Year 2026 volume 9 Issue 9

PDF

155

Cite this Article

BibTeX

Article Info

doi: 10.34133/research.1411

Receive Date：2026-05-14
Online Date：2026-10-16
Published：2026-09-20

Article Data

Affiliations

History

Received：2026-05-14
Revised：2026-08-05
Accepted：2026-08-05

Affiliations

²Key Laboratory of Geriatric Cardiovascular and Cerebrovascular Disease Research (Army Medical University), Ministry of Education, Chongqing 400037, China.

³Department of Cardio-Renal Department, People’s Liberation Army Joint Logistic Support Force 945th Hospital, Ya’an 625000, China.

Corresponding:

^* Address correspondence to: zhaojh@tmmu.edu.cn

References

Share

https://castjournals.cast.org.cn/joweb/research/EN/10.34133/research.1411

Share to

Scan QR to access full text

Cite this article

BibTeX

Citations

表12种不同金属材料的力学参数

科 Family	属数 Number of genus	种数 Number of species	占总种数比例 Percentage of total species (%)	属 Genus	种数 Number of species	占总种数比例 Percentage of total species (%)
鹅膏菌科Amanitaceae	2	11	5.26	鹅膏菌属 Amanita	10	4.78
小菇科 Mycenaceae	2	12	5.74	丝盖伞属 Inocybe	5	2.39
多孔菌科 Polyporaceae	8	14	6.70	蜡蘑属 Laccaria	5	2.39
红菇科 Russulaceae	3	23	11.00	小皮伞属 Marasmius	6	2.87
				小菇属 Mycena	11	5.26
				光柄菇属 Pluteus	5	2.39
				红菇属 Russula	17	8.13
				栓菌属 Trametes	5	2.39

关闭全屏

BibTeX
EndNote
RefWorks
TxT

Fig. 1. Polyunsaturated fatty acid (PUFA) accumulation is observed in fibrous cap vascular smooth muscle cells (VSMCs) of chronic kidney disease (CKD)/ApoE^−/− mice. (A) Different cell types and clusters were identified in arterial tissues from control and patients with CKD through single-cell RNA sequencing. (B) Gene Ontology (GO) functional enrichment analysis of differentially expressed genes (DEGs) in VSMCs of single-cell RNA sequencing. cGMP, cyclic guanosine monophosphate; IFN-α, interferon-α. (C) Heatmap of targeted lipidomics analysis in human VSMCs (hVSMCs) after incubation with normal or CKD serum. (D and E) Quantification of the level of PUFA or monounsaturated fatty acid (MUFA) in hVSMCs after incubation with normal or CKD serum (n = 6). (F to H) Quantification of the level of arachidonic acid (AA), linoleic acid (LA), and linolenic acid (ALA) in hVSMCs after incubation with normal or CKD serum (n = 6). (I to K) Quantification of the level of AA, LA, and ALA in aortic VSMCs of sham/ApoE^−/− and CKD/ApoE^−/− mice (n = 6). (L) Representative hematoxylin and eosin (H&E) staining and spatial targeted lipidomic image in AA, LA, and ALA of the fraction area of aortic root plaques in sham/ApoE^−/− and CKD/ApoE^−/− mice. Scale bars, 100 μm. (M) Quantification of average intensity of root mean square of spatial targeted lipidomic image in AA, LA, and ALA (n = 3). Data represent means ± SD. *P < 0.05, **P < 0.01, and ***P < 0.001, 2-tailed Student’s t test.

Fig. 2. Polyunsaturated fatty acid (PUFA) accumulation promotes ferroptosis in fibrous cap vascular smooth muscle cells (VSMCs) of chronic kidney disease (CKD)/ApoE^−/− mice. (A and B) Cumulative distribution function analysis of ferroptosis suppressor score of VSMCs in control and patients with CKD. (C) The volcano plot shows the differentially expressed genes in aortic VSMCs between sham/ApoE^−/− and CKD/ApoE^-/− mice. (D) Gene set enrichment analysis (GSEA) analysis of ferroptosis gene set in aortic VSMCs of Sham/ApoE^−/− and CKD/ApoE^−/− mice. NES, normalized enrichment score; FDR, false discovery rate. (E) Relative of malondialdehyde (MDA) content in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice (n = 10). (F) Representative images and quantification of relative mean fluorescence intensity (MFI) of dihydroethidium (DHE) staining in aortic root plaques of sham/ApoE^−/− and CKD/ApoE^−/− mice (n = 10). Scale bar, 100 μm. (G) Representative images of hematoxylin and eosin (H&E), 4-hydroxynonenal (4-HNE), and α-smooth muscle actin (α-SMA) staining in fibrous cap VSMCs of sham/ApoE^−/− and CKD/ApoE^−/− mice. Scale bars, 200 μm (H&E) and 10 μm (immunofluorescence [IF]). (H) Quantification of relative mean MFI of 4-HNE in fibrous cap VSMCs of sham/ApoE^−/− and CKD/ApoE^−/− mice (n = 10). (I) Representative transmission electron microscopy (TEM) images of fibrous cap VSMCs in sham/ApoE^−/− and CKD/ApoE^−/− mice. Scale bar, 2 μm. (J and K) Relative of MDA content and the ratio of reduced glutathione (GSH)/oxidized glutathione (GSSG) in human VSMCs (hVSMCs) after incubation with normal or CKD serum (n = 5). (L and M) Representative flow cytometry analysis and the MFI of reactive oxygen species (ROS) and Liperfluo in hVSMCs incubated with normal or CKD serum (n = 3). Data represent means ± SD. ***P < 0.001, 2-tailed Student’s t test.

Fig. 3. Pharmacological inhibition of cytosolic phospholipase A2 (cPLA2) mitigates vascular smooth muscle cell (VSMC) ferroptosis and plaque vulnerability. (A and B) Representative images and quantification of relative mean fluorescence intensity (MFI) of α-smooth muscle actin (α-SMA) and 4-hydroxynonenal (4-HNE) staining in fibrous cap VSMCs of sham/ApoE^−/− and chronic kidney disease (CKD)/ApoE^−/− mice after giripladib treatment (n = 10). Scale bar, 10 μm. (C) Relative of malondialdehyde (MDA) content in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice after giripladib treatment (n = 10). (D) Representative transmission electron microscopy (TEM) images of fibrous cap VSMCs in sham/ApoE^−/− and CKD/ApoE^−/− mice after giripladib treatment. Scale bars, 2 μm. (E) Representative images of α-SMA immunofluorescence (IF) staining in aortic root plaques of sham/ApoE^−/− and CKD/ApoE^−/− mice after giripladib treatment. Scale bar, 10 μm (hematoxylin and eosin [H&E]). (F) Quantification of the fold change of fibrous cap thickness and fibrous cap VSMCs (α-SMA⁺) contents in aortic root plaques of sham/ApoE^−/− and CKD/ApoE^−/− mice after giripladib treatment (n = 10). (G and H) Representative images and quantification of Oil Red O staining in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice after giripladib treatment (n = 10). (I to K) Representative H&E staining images, quantification of mean plaque fraction area and necrotic area percentage within plaques in sham/ApoE^−/− and CKD/ApoE^−/− mice after giripladib treatment (n = 10). Scale bar, 200 μm. Data represent means ± SD. **P < 0.01 and ***P < 0.001, ANOVA.

Fig. 4. Enoyl-coenzyme A hydratase 1 (ECH1) deficiency is responsible for polyunsaturated fatty acid (PUFA) accumulation and vascular smooth muscle cell (VSMC) ferroptosis. (A) Venn diagram shows the intersection of differentially expressed genes (DEGs) from the GSE135626 microarray dataset, ferroptosis regulators, and PUFA metabolism-related genes. (B) Relative mRNA expression levels of ECH1 in arteries of sham/ApoE^−/− and chronic kidney disease (CKD)/ApoE^−/− mice (n = 6). (C) Western blot (WB) analysis and quantification of ECH1 expression levels in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice (n = 6). (D) Representative images of ECH1 and α-smooth muscle actin (α-SMA) staining in fibrous cap VSMCs of sham/ApoE^−/− and CKD/ApoE^−/− mice. Scale bar, 20 μm. (E) Relative mRNA expression levels of ECH1 in human VSMCs (hVSMCs) after incubation with normal or CKD serum (n = 3). (F) WB analysis and quantification of ECH1 expression levels in hVSMCs after incubation with normal or CKD serum (n = 3). (G) Representative images of ECH1 staining in hVSMCs after incubation with normal or CKD serum. Scale bar, 5 μm. (H to J) Quantification of the level of arachidonic acid (AA), linoleic acid (LA), and linolenic acid (ALA) in hVSMCs incubated with normal or CKD serum after ECH1 overexpression (OE) (n = 6). (K and L) Relative of malondialdehyde (MDA) content and the ratio of reduced glutathione (GSH)/oxidized glutathione (GSSG) in hVSMCs incubated with normal or CKD serum after ECH1 overexpression (n = 5). (M) Representative transmission electron microscopy (TEM) images of VSMCs in hVSMCs incubated with normal or CKD serum after ECH1 overexpression. Scale bars, 2 μm. Data represent means ± SD. **P < 0.01 and ***P < 0.001; Student’s t test was applied to (B-C and E-F); one-way analysis of variance (ANOVA) was applied to (H-L). n.s., not significant.

Fig. 5. Human antigen R (HuR) down-regulation-induced enoyl-coenzyme A hydratase 1 (ECH1) deficiency in vascular smooth muscle cells (VSMCs) under chronic kidney disease (CKD) milieus. (A) Detection of mRNA stability of ECH1 in human VSMCs (hVSMCs) after incubation with normal or CKD serum (n = 3). (B) Gene set enrichment analysis (GSEA) analysis of “Regulation of mRNA stability by proteins that bind ARE” gene set in aortic VSMCs of sham/ApoE^−/− and CKD/ApoE^−/− mice. (C) Predicted 6 motifs in the 3′-untranslated region (UTR) of ECH1 mRNA bound by HuR. (D) Western blot (WB) analysis and RNA quantification of HuR expression levels in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice (n = 6). (E) WB analysis and quantification of HuR expression levels in hVSMCs after incubation with normal or CKD serum (n = 3). (F) Detection of mRNA stability of ECH1 in hVSMCs normal or CKD serum after ECH1 overexpression (n = 3). (G) WB analysis and quantification of ECH1 expression in hVSMCs after incubation with normal or CKD serum after HuR overexpression (n = 3). (H) RNA immunoprecipitation (RIP)-quantitative polymerase chain reaction (qPCR) of HuR and ECH1 mRNA in hVSMCs after incubation with normal or CKD serum (n = 3). (I to K) Quantification of the level of arachidonic acid (AA), linoleic acid (LA), and linolenic acid (ALA) in hVSMCs incubated with normal or CKD serum after HuR overexpression (n = 6). (L and M) Relative of malondialdehyde (MDA) content and the ratio of reduced glutathione (GSH)/oxidized glutathione (GSSG) in hVSMCs incubated with normal or CKD serum after HuR overexpression (n = 3). *P < 0.05, **P < 0.01, and ***P < 0.001; Student’s t test (A), (D), and (E); ANOVA was applied to (F) to (M). ActD, actinomycin D; ORF, open reading frame.

Fig. 6. Vascular smooth muscle cell (VSMC)-specific overexpression of enoyl-coenzyme A hydratase 1 (ECH1) reduced ferroptosis of fibrous cap VSMCs. (A) Schematic illustration of the generation of ECH1^R26-LSL conditional knock-in mice via CRISPR–Cas9-mediated homology-directed repair. (B) The protocol of plaque analysis between ECH1^R26-LSL-ApoE^−/− and ECH1^Tagln-OE-ApoE^−/− mice with or without chronic kidney disease (CKD) operation. HFD, high-fat diet. (C to E) Quantification of the level of arachidonic acid (AA), linoleic acid (LA), and linolenic acid (ALA) in arteries of ECH1^R26-LSL-ApoE^−/− and ECH1^Tagln-OE-ApoE^−/− mice with or without CKD operation (n = 6). (F and G) Representative images and quantification of relative mean fluorescence intensity (MFI) of 4-hydroxynonenal (4-HNE) and α-smooth muscle actin (α-SMA) staining in fibrous cap VSMCs in arteries of ECH1^R26-LSL-ApoE^−/− and ECH1^Tagln-OE-ApoE^−/− mice with or without CKD operation (n = 6). Scale bar, 10 μm. (H and I) Western blot (WB) analysis and quantification of 4-HNE expression levels in arteries of ECH1^R26-LSL-ApoE^−/− and ECH1^Tagln-OE-ApoE^−/− mice with or without CKD operation (n = 3). (J) Relative of malondialdehyde (MDA) content in arteries of ECH1^R26-LSL-ApoE^−/− and ECH1^Tagln-OE-ApoE^−/− mice with or without CKD operation (n = 6). (K) Representative transmission electron microscopy (TEM) images of fibrous cap VSMCs in ECH1^R26-LSL-ApoE^−/− and ECH1^Tagln-OE-ApoE^−/− with or without CKD operation. Scale bar, 2 μm. Data represent means ± SD. **P < 0.05, **P < 0.01, and ***P < 0.001, ANOVA.

Fig. 7. Vascular smooth muscle cell (VSMC)-specific overexpression of enoyl-coenzyme A hydratase 1 (ECH1) mitigates atherosclerotic plaque vulnerability. (A) Representative images and quantification of Oil Red O staining in arteries of sham/ApoE^−/− and chronic kidney disease (CKD)/ApoE^−/− mice after ECH1 overexpression (n = 10). Scale bar, 2 μm. (B) Representative images of α-smooth muscle actin (α-SMA) immunofluorescence (IF) staining in aortic root plaques of sham/ApoE^−/− and CKD/ApoE^−/− mice after ECH1 overexpression. Scale bar, 10 μm (hematoxylin and eosin [H&E]). (C) Quantification of the fold change of fibrous cap thickness and fibrous cap VSMCs (α-SMA⁺) contents in aortic root plaques of sham/ApoE^−/− and CKD/ApoE^−/− mice after ECH1 overexpression (n = 10). (D and E) Representative H&E staining and quantification of the fraction area of multiple sections of aortic root plaques in sham/ApoE^−/− and CKD/ApoE^−/− mice after ECH1 overexpression (n = 10). Scale bar, 200 μm. **P < 0.01 and ***P < 0.001, ANOVA.

Fig. 8. Inhibition of acyl-coenzyme A synthetase long-chain family member 4 (ACSL4) alleviates vascular smooth muscle cells (VSMC) ferroptosis and atherosclerotic plaque vulnerability of chronic kidney disease (CKD)/ApoE^−/− mice. (A and B) Representative images and quantification of relative mean fluorescence intensity (MFI) of α-smooth muscle actin (α-SMA) and 4-hydroxynonenal (4-HNE) staining in fibrous cap VSMCs of sham/ApoE^−/− and CKD/ApoE^−/− mice after PRGL493 treatment (n = 10). Scale bar, 10 μm. (C and D) Western blot (WB) analysis and quantification of 4-HNE expression levels in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice after PRGL493 treatment. (E) Relative of malondialdehyde (MDA) content in arteries of sham/ApoE^−/− and CKD/ApoE^-/− mice after PRGL493 treatment (n = 10). (F) Representative transmission electron microscopy (TEM) images of fibrous cap VSMCs in sham/ApoE^−/− and CKD/ApoE^−/− mice after PRGL493 treatment. Scale bar, 2 μm. (G) Representative images of α-SMA immunofluorescence (IF) staining in aortic root plaques of sham/ApoE^−/− and CKD/ApoE^−/− mice after PRGL493 treatment. Scale bar, 10 μm. Quantification of the fold change of fibrous cap thickness and fibrous cap VSMCs (α-SMA⁺) contents in aortic root plaques of sham/ApoE^−/− and CKD/ApoE^−/− mice after PRGL493 treatment (n = 10). (H) Representative images and quantification of Oil Red O staining in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice after PRGL493 treatment. Scale bar, 2 μm. (n = 10). (I to K) Quantification of the level of arachidonic acid (AA), linoleic acid (LA), and linolenic acid (ALA) in arteries of sham/ApoE^−/− and CKD/ApoE^−/− mice after PRGL493 treatment (n = 6).

Articles: Latest Articles; Most Read; Collections

Updates: Events; News; Multimedia

About: About Us

Contact

No. 86 Xueyuan South Road, Haidian District, Beijing

100081

010-62662699(Operation and Technical Support)

qkjq@cast.org.cn

Copyright © 2025 China Association for Science and Technology. All rights reserved. For all open access content, the relevant licensing terms apply.
Sponsored by the Office of the Leading Group for Cybersecurity and Informatization of CAST, and supported by Science and Technology Review Publishing House