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ORIGINAL RESEARCH article

Front. Immunol.

Sec. Autoimmune and Autoinflammatory Disorders : Autoimmune Disorders

Single-cell analysis reveals shared adaptive responses across different types of podocyte injury

Provisionally accepted
Liuxiao  YangLiuxiao Yang1,2Lijun  SunLijun Sun2Wu  LiuWu Liu2Hongliang  RuiHongliang Rui2Haoran  DaiHaoran Dai2Wenbin  LiuWenbin Liu2,3*Baoli  LiuBaoli Liu2,3
  • 1School of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, China
  • 2Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China
  • 3Capital Medical University , Laboratory for Clinical Medicine, Beijing, China

The final, formatted version of the article will be published soon.

Abstract Introduction Podocytes are essential for maintaining the structural and functional integrity of the glomerular filtration barrier. Their damage constitutes a common pathological basis for proteinuria and renal function deterioration in kidney diseases. Podocyte injury exhibits marked heterogeneity in etiology, pathogenic mechanisms, and phenotypic manifestations across distinct kidney diseases, leading to different renal outcomes. However, the molecular underpinnings remain limited. Consequently, single-cell RNA sequencing (scRNA-seq) enables deconstruction of renal cell states with unprecedented resolution. Methods Here, we integrated 16 scRNA-seq samples of human kidney tissues, totaling 73,684 cells from healthy controls and patients with IgA nephropathy (IgAN), idiopathic membranous nephropathy (IMN), and acute kidney injury (AKI). We identified 11 major cell types and analyzed podocyte injury mechanisms among these diseases, as well as their crosstalk within the glomerular niche. Key molecules were confirmed using immunohistochemistry. Results Our analysis identified distinct podocyte injury mechanisms across diseases: HSPG2-mediated signaling from mesangial cells in IgAN, upregulation of extracellular matrix-related genes in IMN, and increased SPP1 signaling within glomeruli in AKI. Despite divergent triggers, podocytes mounted convergent adaptive responses characterized by initial structural disruption, a mitochondria-driven compensatory phase, and subsequent functional dysregulation via multiple stress pathways, culminating in irreversible damage. Conclusion Together, our study reveals both the heterogeneous and shared adaptive responses of injured podocytes through single-cell RNA analysis, providing new insights into disease mechanisms and potential therapeutic targets.

Keywords: Podocyte injury, adaptive response, Transcriptional program, single-cell RNA sequencing, Chronic Kidney Disease, Acute Kidney Injury

Received: 03 Oct 2025; Accepted: 01 Dec 2025.

Copyright: © 2025 Yang, Sun, Liu, Rui, Dai, Liu and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Wenbin Liu

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