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Animal models of idiopathic membranous nephropathy: Recent advances and future perspectives
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Qiuying Liu1, 2, Huixian Bian3, Jianhua Liu1, Lina Wu1, Zhijie Zhang1, Hongli Zhao2, Xiaosong Qin1
Animal Models and Experimental Medicine | 2026, 9(7) : 1325 - 1337
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Animal Models and Experimental Medicine | 2026, 9(7): 1325-1337
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Animal models of idiopathic membranous nephropathy: Recent advances and future perspectives
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Qiuying Liu1, 2, Huixian Bian3, Jianhua Liu1, Lina Wu1, Zhijie Zhang1, Hongli Zhao2, Xiaosong Qin1
Affiliations
  • 1Department of Laboratory Medicine, Shengjing Hospital of China Medical University, Shenyang, China
  • 2Department of Medical Laboratory Technology, Basic Medical Sciences Institute, He University, Shenyang, China
  • 3Department of Anesthesiology, The First Affiliated Hospital of China Medical University, Shenyang, China
Published: 2026-07-28 doi: 10.1002/ame2.70221
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Idiopathic membranous nephropathy (IMN) is one of the main causes of adult nephrotic syndrome. A subset of untreated or inadequately treated patients eventually progress to end-stage renal disease (ESRD), posing a significant clinical challenge. Although the discovery of novel podocyte target antigens has deepened our understanding of IMN pathogenesis, the precise molecular mechanisms remain incompletely elucidated, and effective targeted therapies are still lacking. Animal models play an irreplaceable role in uncovering IMN pathogenesis and developing effective therapies. In recent years, with a deeper understanding of IMN, researchers have successfully established various animal models, including Heymann nephritis (HN), cationic bovine serum albumin (C-BSA), Aminopeptidase A (APA), thrombospondin type 1 domain-containing 7A (THSD7A)-related, and phospholipase A2 receptor (PLA2R)-related IMN models. These models have substantially advanced the simulation of pathological human IMN features. Notably, the development of human PLA2R1-related animal models marks a landmark breakthrough in this field, as these models are the first to recapitulate the immunopathological processes driven by a key human autoantigen in experimental animals. However, current animal models have their own limitations and still cannot fully replicate the complex pathological process of human IMN. This review summarizes recent progress in animal IMN models, analyzes their methods, pathological features, strengths, and limitations, and discusses future directions. Future model development should integrate advanced multi-omics and artificial intelligence (AI) to achieve greater accessibility and precision, enabling the construction of multidimensional models encompassing genetics, environment, and immunity, thereby enabling a leap from "disease simulation" to "personalized treatment".

animal model  /  end-stage renal disease  /  idiopathic membranous nephropathy  /  phospholipase A2 receptor
Qiuying Liu, Huixian Bian, Jianhua Liu, Lina Wu, Zhijie Zhang, Hongli Zhao, Xiaosong Qin. Animal models of idiopathic membranous nephropathy: Recent advances and future perspectives[J]. Animal Models and Experimental Medicine, 2026 , 9 (7) : 1325 -1337 . DOI: 10.1002/ame2.70221
  • Liaoning Provincial Natural Science Foundation Joint Fund(2023-MSLH-077)
Year 2026 volume 9 Issue 7
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Article Info
doi: 10.1002/ame2.70221
  • Receive Date:2025-12-25
  • Online Date:2026-08-06
  • Published:2026-07-28
Article Data
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History
  • Received:2025-12-25
  • Revised:2026-04-06
  • Accepted:2026-04-08
Funding
Liaoning Provincial Natural Science Foundation Joint Fund(2023-MSLH-077)
Affiliations
    1Department of Laboratory Medicine, Shengjing Hospital of China Medical University, Shenyang, China
    2Department of Medical Laboratory Technology, Basic Medical Sciences Institute, He University, Shenyang, China
    3Department of Anesthesiology, The First Affiliated Hospital of China Medical University, Shenyang, China

Corresponding:

Hongli Zhao, Department of Medical Laboratory Technology, Basic Medical Sciences Institute, He University, No. 66 Sishui Street, Hunnan District, Shenyang, China. Email:
Xiaosong Qin, Department of Laboratory Medicine, Shengjing Hospital of China Medical University, No. 36 Sanhao Street, Heping District, Shenyang, China. Email:
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

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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