KN-93, a specific inhibitor of CaMKII inhibits human hepatic stellate cell proliferation in vitro

被引:14
|
作者
An, Ping
Zhu, Jun-Yong
Yang, Yan
Ly, Peng
Tian, Yi-Hao
Chen, Ming-Kai
Luo, He-Sheng
机构
[1] Wuhan Univ, Renmin Hosp, Dept Gastroenterol, Wuhan 430060, Hubei Province, Peoples R China
[2] Wuhan Univ, Renmin Hosp, Educ Adm Off, Wuhan 430060, Hubei Province, Peoples R China
[3] Hubei Xinhua Hosp, Dept Obstet & Gynecol, Wuhan 430015, Hubei Province, Peoples R China
[4] Wuhan Univ, Sch Med, Fac Anat & Embryol, Wuhan 430071, Hubei Province, Peoples R China
关键词
KN-93; human hepatic stellate cells; LX-2; cell proliferation;
D O I
10.3748/wjg.v13.i9.1445
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the effects of KN-93, a CaMK II selective inhibitor on cell proliferation and the expression of p53 or p21 protein in human hepatic stellate cells. METHODS: Human hepatic stellate cells (LX-2) were incubated with various concentrations (0-50 mu mol/L) of KN-93 or its inactive derivative, KN-92. Cell proliferation was measured by CCK-8 assay, and the expression of two cell cycle regulators, p53 and p21, was determined by SDS-PAGE and Western blotting. RESULTS: KN-93 (5-50 mu mol/L) decreased the proliferation of human hepatic stellate cells in a dose-dependent manner from 81.76% (81.76% +/- 2.58% vs 96.63% +/- 2.69%, P < 0.05) to 27.15% (27.15% +/- 2.86% vs 96.59% +/- 2.44%, P < 0.01) after 24 h treatment. Incubation of 10 mu mol/L KN-93 induced the cell growth reduction in a time-dependent manner from 78.27% at 8 h to 11.48% at 48 h. However, KN-92, an inactive derivative of KN-93, did not inhibit cell proliferation effectively. Moreover, analysis of cell cycle regulator expression revealed that KN-93 rather than KN-92 reduced the expression of p53 and p21. CONCLUSION: KN-93 has potent inhibitory effect on proliferation of LX-2 cells by modulating the expression of two special cell cycle regulators, p53 and p21. (C) 2007 The WJG Press. All rights reserved.
引用
收藏
页码:1445 / 1448
页数:4
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