Regulation of differentiation/maturation in vascular smooth muscle cells by hormones and growth factors.

G K Owens, G Wise
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引用次数: 48

Abstract

Smooth muscle cells (SMC) within atherosclerotic lesions show marked alterations in their differentiated properties as compared to normal medial SMC. This process of de-differentiation of SMC has been referred to as "phenotypic modulation", and is characterized by increased growth responsiveness, altered lipid metabolism, increased matrix production, and loss of contractile proteins, all of which can contribute to the development and/or progression of atherosclerotic disease. As such there has been much interest in understanding mechanisms and factors that control the differentiation of the vascular SMC. This paper reviews the effects of growth factors, growth inhibitors, and other extrinsic factors on differentiation/maturation of SMC, with a particular emphasis on consideration of factors that may contribute to abnormal control of SMC differentiation in vascular disease. In addition, we will briefly summarize what is currently known regarding molecular mechanisms that control the coordinate expression of genes encoding for SMC-selective/specific proteins that are required for the differentiated function of the vascular SMC.

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激素和生长因子对血管平滑肌细胞分化/成熟的调控。
与正常内侧平滑肌细胞相比,动脉粥样硬化病变内的平滑肌细胞(SMC)的分化特性有明显改变。SMC的这种去分化过程被称为“表型调节”,其特征是生长反应性增强、脂质代谢改变、基质生成增加和收缩蛋白丧失,所有这些都可能导致动脉粥样硬化疾病的发生和/或进展。因此,人们对了解控制血管SMC分化的机制和因素非常感兴趣。本文综述了生长因子、生长抑制剂等外在因素对SMC分化/成熟的影响,重点讨论了血管疾病中可能导致SMC分化异常控制的因素。此外,我们将简要总结目前已知的控制SMC选择性/特异性蛋白编码基因协调表达的分子机制,这些蛋白是血管SMC分化功能所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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