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 in | Journal of Huazhong University of Science and Technology. Medical sciences Vol. 28; no. 5; pp. 508 - 512 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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 |
Subjects | |
Online Access | Get full text |
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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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1672-0733 1993-1352 |
DOI: | 10.1007/s11596-008-0504-z |