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白藜芦醇诱导 p53 并抑制心肌营养素介导的血管平滑肌细胞分化。

Resveratrol induces p53 and suppresses myocardin-mediated vascular smooth muscle cell differentiation.

机构信息

Department of Internal Medicine, Wayne State University, Detroit, MI 48201, USA.

出版信息

Toxicol Lett. 2010 Nov 30;199(2):115-22. doi: 10.1016/j.toxlet.2010.08.010. Epub 2010 Aug 24.

Abstract

Resveratrol (RSVL), a polyphenolic antioxidant present in red wine, has been shown to provide cardiovascular protection by improving endothelial function and reducing myocardial ischemia. However, little is known about how RSVL affects vascular smooth muscle cells (VSMCs) differentiation. RSVL blocks VSMC proliferation in vitro and neointimal formation following artery injury in vivo. Thus, one might expect that RSVL will promote VSMC differentiation. Unexpectedly, our results in this study show that RSVL induces VSMCs phenotypic modulation; this is characterized by suppressed transcription of SMC-specific marker genes Tagln, Acta2, Myh11, and Smtn in a dose-dependent and time-dependent manner in cultured VSMCs. Consistent with previous studies, RSVL induces the nuclear translocation of p53 and the expression of p53-responsive genes such as Cdkn1a, Gadd45a, Gadd45, and Fas. In an effort to identify the molecular mechanisms whereby RSVL represses VSMC differentiation, we found that RSVL inhibits the transcription of Myocardin (myocd) and Srf, the key VSMC transcriptional regulators. However, knockingdown and overexpressing p53 did not affect RSVL-induced VSMCs phenotypic modulation: this suggests that RSVL may induce VSMC dedifferentiation via p53-independent mechanisms. This study provides the first evidence showing that RSVL induces VSMC dedifferentiation by regulating Myocardin and SRF-mediated VSMC gene transcription.

摘要

白藜芦醇(RSVL)是一种存在于红酒中的多酚抗氧化剂,已被证明通过改善内皮功能和减少心肌缺血来提供心血管保护。然而,人们对 RSVL 如何影响血管平滑肌细胞(VSMCs)分化知之甚少。RSVL 可阻止体外 VSMC 增殖,并可减少体内动脉损伤后的新生内膜形成。因此,人们可能会期望 RSVL 会促进 VSMC 分化。出乎意料的是,我们在这项研究中的结果表明,RSVL 诱导 VSMCs 表型调制;这表现为在培养的 VSMCs 中以剂量和时间依赖性方式抑制 SMC 特异性标记基因 Tagln、Acta2、Myh11 和 Smtn 的转录。与先前的研究一致,RSVL 诱导 p53 的核易位和 p53 反应基因如 Cdkn1a、Gadd45a、Gadd45 和 Fas 的表达。为了确定 RSVL 抑制 VSMC 分化的分子机制,我们发现 RSVL 抑制肌球蛋白重链基因(Myocd)和 Srf 的转录,这是关键的 VSMC 转录调节因子。然而,敲低和过表达 p53 并不影响 RSVL 诱导的 VSMCs 表型调制:这表明 RSVL 可能通过 p53 非依赖性机制诱导 VSMC 去分化。这项研究首次提供证据表明,RSVL 通过调节肌球蛋白重链和 Srf 介导的 VSMC 基因转录来诱导 VSMC 去分化。

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