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Mitochondrial preconditioning of pericytes attenuates pulmonary vascular leakage in sepsis-induced rats
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Zhongyuan DU1, Yiyan LIU2, Daiqin BAO1, Yibo ZHAO3, Juncai GUO4, Yuxuan LI5, Liangming LIU2, Tao LI2, Qingxiang MAO1
Journal of Army Medical University | 2025, 47(23) : 2881 - 2892
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Journal of Army Medical University | 2025, 47(23): 2881-2892
• Military Medicine •
Mitochondrial preconditioning of pericytes attenuates pulmonary vascular leakage in sepsis-induced rats
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Zhongyuan DU1, Yiyan LIU2, Daiqin BAO1, Yibo ZHAO3, Juncai GUO4, Yuxuan LI5, Liangming LIU2, Tao LI2, Qingxiang MAO1
Affiliations
  • 1Department of Anesthesiology,
  • 2National Key Laboratory of Trauma and Chemical Poisoning,Department of War Trauma,Shock and Blood Transfusion,Daping Hospital,Army Medical University,Chongqing
  • 3School of Pharmacy and Bioengineering,Chongqing University of Technology,Chongqing
  • 4School of Basic Medical Sciences,Southwest Medical University,Luzhou,Sichuan
  • 5The First School of Clinical Medicine,Nanjing Medical University,Nanjing,Jiangsu,China
Published: 2025-12-15 doi: 10.16016/j.2097-0927.202507052
Outline
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Objective

To investigate the protective effects of mitochondrial preconditioning in pericytes (PC) against pulmonary vascular leakage in septic rats.

Methods

① 128 specific-pathogen-free SD rats (equal gender, 200±20 g) were randomized into: Sham group (postoperative tail vein injection of 0.5 mL saline), Sepsis (Sep) group (CLP+saline), PC group (CLP+untreated PC: 10⁶ cells/rat), and Mito-PC group (CLP+PC preconditioned with 2 μg mitochondria/10⁴ cells for 12 h). Assessments included: PC lung colonization (flow cytometry), pulmonary barrier function (Evans blue assay), lung histopathology (HE staining), serum organ injury markers [cTnT (cardiac), urea/creatinine (renal)], and inflammatory cytokines (TNF-α, IL-6). ② MSC-derived mitochondria were validated by electron microscopy/flow cytometry; primary retinal PCs from weaned SD rats were purity-verified (confocal microscopy). In vitro groups: Control (PC), Mito-PC, PC+H₂O₂ (0.5 μmol/L, 4 h), and Mito-PC+H₂O₂. Antioxidant capacity was assessed via pentose phosphate pathway (PPP) activity, NADPH levels, G6PD activity, and NADP⁺/NADPH ratio.

Results

① Compared with Sham, Sep group showed significant increase in pulmonary leakage (Evans blue P<0.05), severe lung injury, elevated serum markers (TNF-α, IL-6, cTnT, urea, creatinine all P<0.05), 0% 72 h survival. PC group showed partial improvement (P<0.05). Mito-PC group demonstrated significant reduction in vascular leakage (P<0.05 vs PC group), improved histopathology and organ function (P<0.05), attenuated inflammation (P<0.05), higher 72 h survival rate (P<0.05).② Mitochondrial preconditioning significantly enhanced PPP activation and NADPH-mediated antioxidative capacity, Mito-PC+H₂O₂ vs PC+H₂O₂ showed improved cell viability (P<0.05), Mito-PC vs PC showed increased G6PD activity (P<0.05), decreased NADP⁺/NADPH ratio (P<0.05).

Conclusion

Mitochondrial preconditioning potentiates pericyte-mediated protection against sepsis-induced pulmonary vascular leakage through enhanced pentose phosphate pathway activity. Mitochondrial preconditioning potentiates pericyte-mediated protection against sepsis-induced pulmonary vascular leakage through enhanced pentose phosphate pathway activity.

sepsis  /  pulmonary vascular leakage  /  pericytes transplantation  /  mitochondrial precondition
杜钟媛, 刘奕言, 包代琴, 赵仪博, 郭俊材, 李雨轩, 刘良明, 李涛, 毛庆祥. 线粒体预处理周细胞对脓毒症大鼠肺血管渗漏的保护作用. 陆军军医大学学报, 2025 , 47 (23) : 2881 -2892 . DOI: 10.16016/j.2097-0927.202507052
Zhongyuan DU, Yiyan LIU, Daiqin BAO, Yibo ZHAO, Juncai GUO, Yuxuan LI, Liangming LIU, Tao LI, Qingxiang MAO. Mitochondrial preconditioning of pericytes attenuates pulmonary vascular leakage in sepsis-induced rats[J]. Journal of Army Medical University, 2025 , 47 (23) : 2881 -2892 . DOI: 10.16016/j.2097-0927.202507052
Year 2025 volume 47 Issue 23
17
7
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Article Info
doi: 10.16016/j.2097-0927.202507052
  • Receive Date:2025-07-17
  • Online Date:2026-10-30
  • Published:2025-12-15
Article Data
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History
  • Received:2025-07-17
  • Revised:2025-11-22
Affiliations
    1Department of Anesthesiology,
    2National Key Laboratory of Trauma and Chemical Poisoning,Department of War Trauma,Shock and Blood Transfusion,Daping Hospital,Army Medical University,Chongqing
    3School of Pharmacy and Bioengineering,Chongqing University of Technology,Chongqing
    4School of Basic Medical Sciences,Southwest Medical University,Luzhou,Sichuan
    5The First School of Clinical Medicine,Nanjing Medical University,Nanjing,Jiangsu,China
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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
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