Dalton Cardiovascular Research Center and Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO 65211, USA.
Int J Biochem Cell Biol. 2012 Sep;44(9):1505-10. doi: 10.1016/j.biocel.2012.05.021. Epub 2012 Jun 5.
Contraction of small artery (diameters typically less than 250 μm) vascular smooth muscle cells (VSMCs) plays a critical role in local control of blood flow and arterial pressure through its affect on vascular caliber. Specifically, contraction of small arteries in response to increased intraluminal pressure is referred to as the myogenic response and represents an important role for mechanotransduction. Critical questions remain as to how changes in pressure are sensed by VSMCs and transduced across the cell membrane to tune the contractile state of the cell. Recent studies suggest a pivotal role for interactions between VSMCs and extracellular matrix (ECM) proteins. Thus, pressure-induced deformation of ECM proteins and their cell surface receptors (for example, integrins) may initiate contraction and cytoskeletal remodeling through modulation of ion channels, membrane depolarization, increased intracellular Ca(2+) and actomyosin crossbridge cycling. Importantly, it is argued that the contractile properties of small artery VSMCs reflect an intimate and integrated interaction with their extracellular environment and the three-dimensional structure of the vessel wall.
小动脉(直径通常小于 250μm)血管平滑肌细胞(VSMCs)的收缩在通过影响血管口径对局部血流和动脉压的控制中起着关键作用。具体而言,小动脉对腔内压力增加的反应性收缩称为肌源性反应,这代表了机械转导的重要作用。目前仍然存在一些关键问题,即 VSMCs 如何感知压力变化,并将其跨细胞膜转导,以调节细胞的收缩状态。最近的研究表明,VSMCs 与细胞外基质(ECM)蛋白之间的相互作用起着关键作用。因此,细胞外基质蛋白及其细胞表面受体(例如整合素)的压力诱导变形可能通过调节离子通道、膜去极化、增加细胞内 Ca(2+)和肌球蛋白交联循环来启动收缩和细胞骨架重塑。重要的是,有人认为小动脉 VSMCs 的收缩特性反映了它们与细胞外环境以及血管壁的三维结构的密切和综合相互作用。