High glucose promotes the CTGF expression in human mesangial cells via serum and glucocorticoid-induced kinase 1 pathway

Summary The role of serum and glucocorticoid-induced kinase 1 (SGK1) pathway in the connective tissue growth factor (CTGF) expression was investigated in cultured human mesangial cells (HMCs) under high glucose. By using RT-PCR and Western blot, the effect of SGK1 on the CTGF expression in HMCs unde...

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Published inJournal of Huazhong University of Science and Technology. Medical sciences Vol. 28; no. 5; pp. 508 - 512
Main Authors Wang, Quansheng, Zhang, Ali, Li, Renkang, Liu, Jianguo, Xie, Jiwen, Deng, Anguo, Feng, Yuxi, Zhu, Zhonghua
Format Journal Article
LanguageEnglish
Published Heidelberg Huazhong University of Science and Technology 01.10.2008
Department of Integrated Chinese Medicine and Western Medicine,Wuhan 430022, China%Department of Radiotherapy and Chemotherapy, Zhongnan Hospital Wuhan University, Wuhan 430071, China%Department of Nephrology, Union Hospital TongJi Medical College, Huazhong University of Science and Technology, Wuhan 430022, China
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Summary:Summary The role of serum and glucocorticoid-induced kinase 1 (SGK1) pathway in the connective tissue growth factor (CTGF) expression was investigated in cultured human mesangial cells (HMCs) under high glucose. By using RT-PCR and Western blot, the effect of SGK1 on the CTGF expression in HMCs under high glucose was examined. Overexpression of active SGK1 in HMCs transfected with p IRES 2 -EGFP- S422D hSGK1 (SD) could increase the expression of phosphorylated SGK1 and CTGF as compared with HMCs groups transfected with p IRES 2 -EGFP (FP) under high glucose or normal glucose. Overexpression of inactive SGK1 in HMCs transfected with p IRES 2 -EGFP- K127N hSGK1 (KN) could decrease phosphorylated SGK1 and CTGF expression as compared with HMCs groups transfected with FP under high glucose. In conclusion, these results suggest that high glucose-induced CTGF expression is mediated through the active SGK1 in HMCs.
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ISSN:1672-0733
1993-1352
DOI:10.1007/s11596-008-0504-z