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作 者:黄文勇[1] 曾骏文[1] 刘奕志[1] 吴明星[1]
出 处:《中国病理生理杂志》2005年第12期2443-2446,共4页Chinese Journal of Pathophysiology
基 金:广东省科技计划项目(NO.20030087)
摘 要:目的:探讨在绿茶提取物表没食子儿茶素没食子酸酯(EGCG)抑制兔晶状体上皮细胞增殖过程中, MEK/ERK1/2(MITOGEN-ACTIVATED PROTEIN KINASE KINASE,MAPKK,MEK;EXTRACELLULAR SIGNAL-REGULATED KINASE,ERK)及C-JUN 氨基末端激酶(C-JUN NH2-TERMINAL PROTEIN KINASE,JNK)信号转导通路的作用。方法:实验按EGCG浓度分50、100和 200 ΜMOL/L3组。预先分别加入25、50 ΜMOL/L的ERK活性拮抗剂PD980059孵育1 H;用噻唑蓝比色法(MTT比色法) 测定晶状体上皮细胞增殖;用蛋白质免疫沉淀法(WESTERN BLOTTING)法检测ERK及JNK的磷酸化水平。结果:(1) PD980059能明显增强EGCG抑制晶状体上皮细胞增殖的作用,呈浓度依赖性。(2)晶状体上皮细胞内磷酸化的ERK 基础水平高。加入EGCG后其活性升高,随后逐渐回降,但始终高于基础水平;ERK的活化水平也随EGCG浓度的增加而增高。(3)细胞内JNK的54 KD亚型磷酸化的基础水平较低而46 KD亚型的较高;呈剂量与时间依赖性。结论: EGCG可能部分通过调节ERK和JNK的磷酸化水平而抑制晶状体上皮细胞的增殖。AIM: ( - ) - Epigallocatechin- 3 - gallate (EGCG) is an extract from green tea, it could strongly inhibit the growth of cultured rabbit lens epithelial cells. This study explored the role of MEK1/ERK1/2 and JNK pathways in the prolifera-, tion inhibition of rabbit lens epithelial ceils (LECs) induced by EGCG. METHODS: MTI' colormetric assay was used to study the LECs growth inhibition. Western blotting were applied to study the kinsae phnsphorylation level of ERK and JNK. RESULTS: (1) ERK activity blocker PD980059 could enhance EGCG - induced inhibition effect on proliferation of LECs compared with control groups in a dose - dependent manner. (2) Basic phnsphorylation level of ERK was fairy high in LECs; and was increased by EGCG in a dose - dependent manner. The ERK phosphorylation reached its peak immediately after EGCG was added and stayed high even at the end of the test. (3) The basic phosphorylation - level of 54 kD JNK was weak but 46 kD was high in LECs; EGCG increased phnsphorylated JNK level in a tinre and concentration - dependent manner in our test. CONCLUSION: It is suggested that the LEC proliferation inhibition induced by EGCG is, at least in part, through ERK and JNK pathways.
关 键 词:表没食子儿茶素没食子酸酯 晶状体上皮细胞 有丝分裂素激活蛋白激酶类
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