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Calcineurin inhibitors ameliorate PAN ‐induced podocyte injury through the NFAT–Angptl4 pathway
Author(s) -
Shen Xiujin,
Zhang Ying,
Lin Chuan,
Weng Chunhua,
Wang Yucheng,
Feng Shi,
Wang Cuili,
Shao Xue,
Lin Weiqiang,
Li Bingjue,
Wang Haibing,
Chen Jianghua,
Jiang Hong
Publication year - 2020
Publication title -
the journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.964
H-Index - 184
eISSN - 1096-9896
pISSN - 0022-3417
DOI - 10.1002/path.5512
Subject(s) - podocyte , synaptopodin , podocin , angptl4 , nfat , gene knockdown , cancer research , chemistry , microbiology and biotechnology , diabetic nephropathy , medicine , pharmacology , endocrinology , calcineurin , biology , proteinuria , kidney , apoptosis , biochemistry , transplantation , gene
Podocyte injury plays a vital role in proteinuria and nephrotic syndrome. Calcineurin (CaN) inhibitors are effective in reducing proteinuria. However, their molecular mechanism is still not fully understood. Angiopoietin‐like‐4 (ANGPTL4) is a secreted protein that mediates proteinuria in podocyte‐related nephropathy. In this study, we established a puromycin aminonucleoside (PAN)‐induced minimal‐change disease (MCD) rat model and a cultured podocyte injury model. We found that CaN inhibitors protected against PAN‐induced podocyte injury, accompanied by an inhibition of Nfatc1 and Angptl4 both in vivo and in vitro . Nfatc1 overexpression and knockdown experiments indicated that Angptl4 was regulated by Nfatc1 in podocytes. ChIP assays further demonstrated that Nfatc1 increased Angptl4 expression by binding to the Angptl4 promoter. In addition, overexpression and knockdown of Angptl4 revealed that Angptl4 directly induced rearrangement of the cytoskeleton of podocytes, reduced the expression of synaptopodin, and enhanced PAN‐induced podocyte apoptosis. Furthermore, in a cohort of 83 MCD and 94 membranous nephropathy (MN) patients, we found increased expression of serum ANGPTL4 compared to 120 healthy controls, and there were close correlations between serum ANGPTL4 and Alb, urinary protein, urinary Alb, eGFR, Scr, and BUN in MCD patients. No obvious correlation was found in MN patients. Immunofluorescence studies indicated that increased ANGPTL4 in MCD and MN patients was located mostly in podocytes. In conclusion, our results demonstrate that CaN inhibitors ameliorate PAN‐induced podocyte injury by targeting Angptl4 through the NFAT pathway, and Angptl4 plays a vital role in podocyte injury and is involved in human podocyte‐related nephropathy. © 2020 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.