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

机译:KN-93CaMKII的特异性抑制剂体外抑制人肝星状细胞增殖

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摘要

AIM: To investigate the effects of KN-93, a CaMKII 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 μmol/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 μmol/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 μmol/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.
机译:目的:研究CaMKII选择性抑制剂KN-93对人肝星状细胞增殖及p53或p21蛋白表达的影响。方法:将人肝星状细胞(LX-2)在不同浓度下孵育(0 -50μmol/ L)的KN-93或其非活性衍生物KN-92。结果:KN-93(5-50μmol/ L)抑制CCK-8的增殖,并通过SDS-PAGE和Western blotting检测两种细胞周期调节子p53和p21的表达。人肝星状细胞以剂量依赖性方式从81.76%(81.76%±2.58%vs 96.63%±2.69%,P <0.05)到27.15%(27.15%±2.86%vs 96.59%±2.44%,P <0.01)治疗24小时后。 10μmol/ L KN-93的孵育以时间依赖性方式诱导细胞生长减少,从8小时的78.27%降至48小时的11.48%。但是,KN-92的无活性衍生物KN-92不能有效地抑制细胞增殖。此外,对细胞周期调节因子表达的分析表明,KN-93而非KN-92降低了p53和p21的表达。结论:KN-93通过调节两个特殊细胞的表达对LX-2细胞的增殖具有有效的抑制作用。循环调节器p53和p21。

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