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绿茶多酚表没食子儿没食子酸酯通过抑制基质金属蛋白酶-2(MMP-2)的表达及其激活来抑制大鼠肝星状细胞的侵袭。

Green tea polyphenol epigallocatechin-3-gallate suppresses rat hepatic stellate cell invasion by inhibition of MMP-2 expression and its activation.

作者信息

Zhen Mao-chuan, Huang Xiao-hui, Wang Qian, Sun Kai, Liu Yun-jian, Li Wen, Zhang Long-juan, Cao Liang-qi, Chen Xi-ling

机构信息

Department of Hepatobiliary Surgery, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.

出版信息

Acta Pharmacol Sin. 2006 Dec;27(12):1600-7. doi: 10.1111/j.1745-7254.2006.00439.x.

Abstract

AIM

Epigallocatechin-3-gallate (EGCG) is the major component of green tea polyphenols, whose wide range of biological properties includes anti-fibrogenic activity. Matrix metalloproteinases (MMP) that participate in extracellular matrix degradation are involved in the development of hepatic fibrosis. The present study investigates whether EGCG inhibits activation of the major gelatinase matrix metalloproteinase-2 (MMP-2) in rat hepatic stellate cells (HSC).

METHODS

The expression of MMP-2, tissue inhibitors of metalloproteinases-2 (TIMP-2), and membrane-type 1-MMP (MT1-MMP) was assessed by RT-PCR and Western blot analyses. MMP-2 activity was evaluated by zymography and MT1-MMP activity was assessed by an enzymatic assay. HSC migration was measured by a wound healing assay and cell invasion was performed using Transwell cell culture chambers.

RESULTS

The expression of MMP-2 mRNA and protein in HSC was substantially reduced by EGCG treatment. EGCG treatment also reduced concanavalin A (ConA)-induced activation of secreted MMP-2 and reduced MT1-MMP activity in a dose-dependent manner. In addition, EGCG inhibited either HSC migration or invasion.

CONCLUSION

The abilities of EGCG to suppress MMP-2 activation and HSC invasiveness suggest that EGCG may be useful in the treatment and prevention of hepatic fibrosis.

摘要

目的

表没食子儿茶素-3-没食子酸酯(EGCG)是绿茶多酚的主要成分,其广泛的生物学特性包括抗纤维化活性。参与细胞外基质降解的基质金属蛋白酶(MMP)与肝纤维化的发展有关。本研究调查EGCG是否抑制大鼠肝星状细胞(HSC)中主要明胶酶基质金属蛋白酶-2(MMP-2)的激活。

方法

通过逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹分析评估MMP-2、金属蛋白酶组织抑制剂-2(TIMP-2)和膜型1-MMP(MT1-MMP)的表达。通过酶谱法评估MMP-2活性,通过酶活性测定评估MT1-MMP活性。采用伤口愈合试验测量HSC迁移,并使用Transwell细胞培养小室进行细胞侵袭实验。

结果

EGCG处理可显著降低HSC中MMP-2 mRNA和蛋白质的表达。EGCG处理还以剂量依赖性方式降低伴刀豆球蛋白A(ConA)诱导的分泌型MMP-2的激活,并降低MT1-MMP活性。此外,EGCG抑制HSC迁移或侵袭。

结论

EGCG抑制MMP-2激活和HSC侵袭的能力表明,EGCG可能对肝纤维化的治疗和预防有用。

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