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Effects of Estrogen Receptor Alpha on Vascular Smooth Muscle Cell SM22

机译:雌激素受体α对血管平滑肌细胞SM22的影响

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Myocardin and associated transcription factor (Myocardin-Related Transcription Factors, MRTFs) by serum response factor (SRF) together constitute the composition of molecular differentiation of muscle cell switch. This paper focuses on the vascular smooth muscle cells (vascular smooth muscle cells, VSMCs), breast cancer cell lines MCF-7 and African green monkey kidney cell line COS-7 as the research object, using cellular and molecular biological methods to study the transcription factor Myocardin and Estrogen receptor α (ER α) in the regulation of differentiation of vascular smooth muscle cell function. The luciferase reporter assay in COS-7 and MCF-7 cell lines and VSMCs (Luciferase Report assay) method to study the ER alpha for Myocardin differentiation ability, the results showed that ER α can inhibit SM22 α Myocardin for transcription activation. At the same time, the expression of estradiol and tamoxifen treatment by transfection group for detection of SM22 and found that blocking the ER alpha for the inhibitory effect of Myocardin differentiation ability can be ER alpha antagonist tamoxi.
机译:血清响应因子(SRF)的Myocardin和相关的转录因子(Myocardin相关转录因子,MRTF)共同构成肌细胞开关分子分化的组成。本文重点介绍血管平滑肌细胞(血管平滑肌细胞,VSMC),乳腺癌细胞系MCF-7和非洲绿猴肾细胞系COS-7作为研究对象,使用细胞和分子生物学方法研究转录血管平滑肌细胞功能分化调节中的因子肌陶器和雌激素受体α(ERα)。 COS-7和MCF-7细胞系和VSMCs(Luciferase报告测定)方法中的荧光素酶报告器测定方法研究ERα用于心肌素分化能力,结果表明,ERα可以抑制SM22α心肌蛋白用于转录激活。同时,转染基团的雌二醇和三莫昔芬治疗检测SM22的表达,发现阻断ER alpha用于心肌蛋白分化能力的抑制作用可以是ERα拮抗剂Tamoxi。

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