Chettimada Sukrutha, Yang Jincheng, Moon Hyung-Geun, Jin Yang
Division of Pulmonary and Critical Care, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, United States.
World J Respirol. 2015 Jul 28;5(2):126-134. doi: 10.5320/wjr.v5.i2.126.
Caveolae are flask-shaped invaginations of cell membrane that play a significant structural and functional role. Caveolae harbor a variety of signaling molecules and serve to receive, concentrate and transmit extracellular signals across the membrane. Caveolins are the main structural proteins residing in the caveolae. Caveolins and another category of newly identified caveolae regulatory proteins, named cavins, are not only responsible for caveolae formation, but also interact with signaling complexes in the caveolae and regulate transmission of signals across the membrane. In the lung, two of the three caveolin isoforms, ., cav-1 and -2, are expressed ubiquitously. Cavin protein family is composed of four proteins, named cavin-1 (or PTRF for polymerase Ⅰ and transcript release factor), cavin-2 (or SDPR for serum deprivation protein response), cavin-3 (or SRBC for sdr-related gene product that binds to-c-kinase) and cavin-4 (or MURC for muscle restricted coiled-coiled protein or cavin-4). All the caveolin and cavin proteins are essential regulators for caveolae dynamics. Recently, emerging evidence suggest that caveolae and its associated proteins play crucial roles in development and progression of pulmonary hypertension. The focus of this review is to outline and discuss the contrast in alteration of cav-1 (cav-1),-2 and cavin-1 (PTRF) expression and downstream signaling mechanisms between human and experimental models of pulmonary hypertension.
小窝是细胞膜呈烧瓶状的内陷结构,发挥着重要的结构和功能作用。小窝含有多种信号分子,用于接收、浓缩并跨膜传递细胞外信号。小窝蛋白是存在于小窝中的主要结构蛋白。小窝蛋白以及另一类新发现的小窝调节蛋白(称为小窝结合蛋白)不仅负责小窝的形成,还与小窝中的信号复合物相互作用,并调节跨膜信号传递。在肺中,三种小窝蛋白亚型中的两种,即小窝蛋白-1(cav-1)和小窝蛋白-2,广泛表达。小窝结合蛋白家族由四种蛋白质组成,分别称为小窝结合蛋白-1(或聚合酶Ⅰ和转录释放因子的PTRF)、小窝结合蛋白-2(或血清剥夺蛋白反应的SDPR)、小窝结合蛋白-3(或与c激酶结合的sdr相关基因产物的SRBC)和小窝结合蛋白-4(或肌肉限制性卷曲螺旋蛋白的MURC或小窝结合蛋白-4)。所有的小窝蛋白和小窝结合蛋白都是小窝动态变化的重要调节因子。最近,越来越多的证据表明,小窝及其相关蛋白在肺动脉高压的发生和发展中起关键作用。本综述的重点是概述和讨论人类和实验性肺动脉高压模型中小窝蛋白-1(cav-1)、小窝蛋白-2和小窝结合蛋白-1(PTRF)表达变化及下游信号传导机制的差异。