2. Academic Validation
  3. Klotho inhibits PKCα/p66SHC-mediated podocyte injury in diabetic nephropathy

Klotho inhibits PKCα/p66SHC-mediated podocyte injury in diabetic nephropathy

  • Mol Cell Endocrinol. 2019 Aug 20;494:110490. doi: 10.1016/j.mce.2019.110490.
Wei Jiang 1,  Tangli Xiao 1,  Wenhao Han 1,  Jiachuan Xiong 1,  Ting He 1,  Yong Liu 1,  Yinghui Huang 1,  Ke Yang 1,  Xianjin Bi 1,  Xinli Xu 1,  Yanlin Yu 1,  Yan Li 1,  Jun Gu 2,  Jingbo Zhang 1,  Yunjian Huang 1,  Bo Zhang 3,  Jinghong Zhao 4
Affiliations

Affiliations

  • 1 Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
  • 2 State Key Laboratory of Protein and Plant Gene Research, College of Life Science, Peking University, Beijing, China.
  • 3 Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, China. Electronic address: bo_zhang@tmmu.edu.cn.
  • 4 Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, China. Electronic address: zhaojh@tmmu.edu.cn.
PMID: 31207271 DOI: 10.1016/j.mce.2019.110490
Abstract

Diabetic nephropathy (DN) is a progressive disease, the main pathogeny of which is podocyte injury. As a calcium-dependent serine/threonine protein kinase involved in podocyte injury, protein kinase C isoform α (PKCα) was reported to regulate the phosphorylation of p66SHC. However, the role of PKCα/p66SHC in DN remains unknown. Klotho, an Anti-aging protein with critical roles in protecting kidney, is expressed predominantly in the kidney and secreted in the blood. Nonetheless, the mechanism underlying amelioration of podocyte injury by Klotho in DN remains unclear. Our data showed that Klotho was decreased in STZ-treated mice and was further declined in diabetic KL ± mice. As expected, Klotho deficiency aggravated diabetes-induced proteinuria and podocyte injury, accompanied by the activation of PKCα and p66SHC. In contrast, overexpression of Klotho partially ameliorated PKCα/p66SHC-mediated podocyte injury and proteinuria. In addition, in vitro experiments showed that activation of PKCα and subsequently increased intracellular Reactive Oxygen Species (ROS) was involved in podocytic Apoptosis induced by high glucose (HG), which could be partially reversed by Klotho. Hence, we conclude that Klotho might inhibit PKCα/p66SHC-mediated podocyte injury in diabetic nephropathy.

Keywords

Diabetic nephropathy; Klotho; PKCα; Podocyte; Reactive oxygen species.

Figures
Products