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Selective Inhibitory Effect of Epigallocatechin-3-gallate on Migration of Vascular Smooth Muscle Cells

机译:表没食子儿茶素-3-没食子酸酯对血管平滑肌细胞迁移的选择性抑制作用

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摘要

In order to prevent restenosis after angioplasty or stenting, one of the most popular targets is suppression of the abnormal growth and excess migration of vascular smooth muscle cells (VSMCs) with drugs. However, the drugs also adversely affect vascular endothelial cells (VECs), leading to the induction of late thrombosis. We have investigated the effect of epigallocatechin-3-gallate (EGCG) on the proliferation and migration of VECs and VSMCs. Both cells showed dose-dependent decrease of viability in response to EGCG while they have different IC50 values of EGCG (VECs, 150 μM and VSMCs, 1050 μM). Incubating both cells with EGCG resulted in significant reduction in cell proliferation irrespective of cell type. The proliferation of VECs were greater affected than that of VSMCs at the same concentrations of EGCG. EGCG exerted differential migration-inhibitory activity in VECs vs. VSMCs. The migration of VECs was not attenuated by 200 μM EGCG, but that of VSMCs was significantly inhibited at the same concentration of EGCG. It is suggested that that EGCG can be effectively used as an efficient drug for vascular diseases or stents due to its selective activity, completely suppressing the proliferation and migration of VSMCs, but not adversely affecting VECs migration in blood vessels.
机译:为了防止血管成形术或支架置入术后再狭窄,最受欢迎的目标之一是用药物抑制血管平滑肌细胞(VSMC)的异常生长和过度迁移。但是,这些药物也会对血管内皮细胞(VEC)产生不利影响,从而导致晚期血栓形成。我们已经研究了表没食子儿茶素-3-没食子酸酯(EGCG)对VEC和VSMC增殖和迁移的影响。两种细胞对EGCG的反应均显示出剂量依赖性的活力降低,而EGCG的IC50值不同(VEC为150μM,VSMC为1050μM)。将两种细胞与EGCG一起孵育均会导致细胞增殖显着降低,而与细胞类型无关。在相同的EGCG浓度下,VECs的增殖比VSMCs受到的影响更大。 EGCG在VEC与VSMC中发挥了不同的迁移抑制活性。 200μMEGCG不会减弱VEC的迁移,但是在相同浓度的EGCG下VSMC的迁移却受到显着抑制。提示EGCG由于具有选择性活性,可以有效地用作血管疾病或支架的有效药物,可以完全抑制VSMC的增殖和迁移,但对VEC在血管中的迁移没有不利影响。

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