Parmacek Michael S
University of Pennsylvania Cardiovascular Institute and Department of Medicine, Philadelphia, Pennsylvania 19104, USA.
J Clin Invest. 2009 Sep;119(9):2526-8. doi: 10.1172/JCI40503. Epub 2009 Aug 17.
VSMCs exhibit the remarkable plasticity required for development and adaptation of the cardiovascular system. The capacity of VSMCs to modulate their phenotype has evolved to facilitate angiogenesis and wound healing, but it has also been implicated in the pathogenesis of atherosclerosis, restenosis, posttransplant arteriopathy, and pulmonary hypertension. In this issue of the JCI, Boettger and colleagues report that the recently discovered Mir143/145 gene cluster promotes acquisition of the contractile phenotype of murine VSMCs (see the related article beginning on page 2634). These VSMC-restricted microRNAs, which target unique combinations of SMC genes, provide an efficient mechanism to fine-tune cardiovascular homeostasis and the response of the vessel wall to injury. This important discovery will open the door to new avenues of investigation and potentially future therapies for vascular diseases.
血管平滑肌细胞表现出心血管系统发育和适应所需的显著可塑性。血管平滑肌细胞调节其表型的能力已经进化,以促进血管生成和伤口愈合,但它也与动脉粥样硬化、再狭窄、移植后动脉病变和肺动脉高压的发病机制有关。在本期《临床研究杂志》中,博特格及其同事报告称,最近发现的Mir143/145基因簇促进了小鼠血管平滑肌细胞收缩表型的获得(见第2634页开始的相关文章)。这些血管平滑肌细胞特异性的微小RNA靶向平滑肌细胞基因的独特组合,为微调心血管稳态和血管壁对损伤的反应提供了一种有效的机制。这一重要发现将为血管疾病的新研究途径和潜在的未来治疗打开大门。