Loss of PTEN promotes podocyte cytoskeletal rearrangement, aggravating diabetic nephropathy

• Published in: The Journal of pathology Vol. 236; no. 1; pp. 30 - 40
• Main Authors: Lin, Jamie S, Shi, Yuanyuan, Peng, Hui, Shen, Xiaojie, Thomas, Sandhya, Wang, Yanlin, Truong, Luan D, Dryer, Stuart E, Hu, Zhaoyong, Xu, Jing
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01.05.2015; Wiley Subscription Services, Inc
• Subjects: Albuminuria - metabolism; Animals; cytoskeletal rearrangement; Cytoskeleton - metabolism; Cytoskeleton - pathology; Diabetic Nephropathies - metabolism; Diabetic Nephropathies - pathology; diabetic nephropathy; Disease Models, Animal; Glomerular Mesangium - metabolism; Humans; Membrane Proteins - metabolism; Mice; podocyte; Podocytes - metabolism; Podocytes - pathology; PTEN; PTEN Phosphohydrolase - metabolism; cytoskeletal rearrangement; PTEN; diabetic nephropathy; podocyte
• ISSN: 0022-3417; 1096-9896
• DOI: 10.1002/path.4508

In diabetic nephropathy (DN), podocyte cytoskeletal rearrangement occurs followed by podocyte effacement and the development of proteinuria. PTEN (phosphatase and tensin homologue) is a ubiquitously expressed phosphatase that plays a critical role in cell proliferation, cytoskeletal rearrangement, and motility. In mouse models of diabetes mellitus, PTEN expression is reportedly decreased in mesangial cells, contributing to expansion of the mesangial matrix, but how PTEN in the podocyte influences the development of DN is unknown. We observed that PTEN expression is down‐regulated in the podocytes of diabetic db/db mice and patients with DN. In cultured podocytes, PTEN inhibition caused actin cytoskeletal rearrangement and this response was associated with unbalanced activation of the small GTPases Rac1/Cdc42 and RhoA. In mice treated with PTEN inhibitor, actin cytoskeletal rearrangement occurred in podocytes and was accompanied by increased albumin excretion. We also created mice with an inducible deletion of PTEN selectively in podocytes. These mice exhibited increased albumin excretion and moderate foot process effacement. When the mice were challenged with a high fat diet, podocyte‐specific knockout of PTEN resulted in substantially increased proteinuria and glomeruloclerosis compared to control mice fed a high fat diet or mice with PTEN deletion fed a normal diet. These results indicate that PTEN is involved in the regulation of cytoskeletal rearrangement in podocytes and that loss of PTEN predisposes to the development of proteinuria and DN. Copyright © 2015 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.