Vanadate enhances leptin-induced activation of JAK/STAT pathway in CHO cells

被引:21
作者
Kita, A
Uotani, S
Kuwahara, H
Takahashi, R
Oshima, K
Yamasaki, H
Mizuguchi, H
Hayakawa, T
Nagayama, Y
Yamaguchi, Y
Eguchi, K
机构
[1] Nagasaki Univ, Sch Med, Dept Internal Med 1, Nagasaki 8528501, Japan
[2] Natl Inst Hlth Sci, Div Cellular & Gene Therapy Prod, Tokyo 1588501, Japan
[3] Nagasaki Univ, Sch Med, Dept Pharmacol 1, Nagasaki 8528523, Japan
关键词
D O I
10.1016/S0006-291X(03)00264-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Leptin, the product of the ob gene, is an adipocyte-derived hormone that plays a key role in the control of food intake and energy expenditure. Leptin acts through receptors that belong to a member of the class I cytokine receptor family. It has been demonstrated that the SH2 domain-containing tyrosine phosphatase 2 (SHP-2) negatively regulates STAT3-mediated transcriptional activation through long form leptin receptor (OBRb). Vanadate has been shown to be a potent and selective inhibitor of PTPase activity in vitro. In this study, we have demonstrated that vanadate increases leptin-induced JAK2 and STAT3 phosphorylation in CHO cells expressing OBRb. The increased leptin-dependent luciferase activity of SOCS3 gene was also seen in vanadate-treated cell. Furthermore, vanadate reversed the inhibitory effects of SOCS3 on leptin-induced STAT3 phosphorylation. The present findings suggest that PTP inhibitors including vanadate and vanadate-derived compounds could be used as a therapeutic agent in the treatment of obesity. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:805 / 809
页数:5
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