Enhanced glycogen synthase kinase-3 beta activity mediates podocyte apoptosis under diabetic conditions
- Authors
- Paeng, Jisun; Chang, Jae Hyun; Lee, Sun Ha; Nam, Bo Young; Kang, Hye-Young; Kim, Seonghun; Oh, Hyung Jung; Park, Jung Tak; Han, Seung Hyeok; Yoo, Tae-Hyun; Kang, Shin-Wook
- Issue Date
- Dec-2014
- Publisher
- SPRINGER
- Keywords
- GSK-3 beta; Diabetic nephropathy; Podocyte; Apoptosis
- Citation
- APOPTOSIS, v.19, no.12, pp.1678 - 1690
- Journal Title
- APOPTOSIS
- Volume
- 19
- Number
- 12
- Start Page
- 1678
- End Page
- 1690
- URI
- https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12066
- DOI
- 10.1007/s10495-014-1037-5
- ISSN
- 1360-8185
- Abstract
- Glycogen synthase kinase-3 beta (GSK-3 beta) is involved in the pathogenesis of various kidney diseases. This study was undertaken to examine the changes in GSK-3 beta activity in podocytes under diabetic conditions and to elucidate the functional role of GSK-3 beta in podocyte apoptosis. In vivo, 32 rats were injected with either diluent (n = 16, C) or with streptozotocin intraperitoneally (n = 16, DM), and 8 rats from each group were treated with 6-bromoindirubin-3'-oxime (BIO) for 3 months. In vitro, immortalized mouse podocytes were exposed to 5.6 mM glucose or 30 mM glucose (HG) with or without 10 mu M BIO. Western blot analysis and TUNEL or Hoechst 33342 staining were performed to identify apoptosis. Urinary albumin excretion was significantly higher in DM rats, and this increase was significantly abrogated in DM rats by BIO treatment. The protein expression of Tyr216-phospho-GSK-3 beta was significantly increased in DM glomeruli and in cultured podocytes exposed to HG. Western blot analysis revealed that the protein expression of Bax and active fragments of caspase-3 were significantly increased, whereas phospho-Akt, beta-catenin, and Bcl-2 protein expression were significantly decreased in DM glomeruli and HG-stimulated podocytes. Apoptosis, determined by TUNEL assay and Hoechst 33342 staining, was also significantly increased in podocytes under diabetic conditions. The changes in the expression of apoptosis-related molecules and the increase in the number of apoptotic cells in DM glomeruli as well as in HG-stimulated podocytes were significantly ameliorated by BIO. These findings suggest that enhanced GSK-3 beta activity within podocytes under diabetic conditions is associated with podocyte loss in diabetic nephropathy.
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