肺动脉高压
右心室肥大
细胞凋亡
缺氧(环境)
肌肉肥大
细胞生长
胶溶蛋白
生物
肺动脉
癌症研究
内科学
病理
内分泌学
医学
细胞生物学
肌动蛋白
化学
有机化学
氧气
生物化学
遗传学
作者
Xiaoling Xu,Huihui Hu,Xiaohua Wang,Ye Wu,Hua Su,Yanjie Hu,Liu Dong,Ruifeng Zhang,Kejing Ying
标识
DOI:10.3109/01902148.2016.1160304
摘要
Actin-binding protein capping protein gelsolin-like (CapG) was preferentially expressed in human pulmonary arterial smooth muscle cells (PASMCs) under hypoxia, and reduced CapG expression was accompanied by impaired migration ability in vitro. We intended to investigate the effects of CapG on rat PASMCs and hypoxia-induced pulmonary hypertension (HPH) rat model.We investigated the effect of RNA interference-medicated down-regulation of CapG expression in rat PASMCs as well as in HPH rat model. The proliferation, apoptosis and cell cycle of PASMCs were evaluated. The HPH rat model was established by intratracheal instillation of lentiviral vector and subsequent hypoxia exposure for four weeks. Right ventricular systolic pressure, right ventricular hypertrophy and the percentage of medial wall thickness were measured to evaluate the development of HPH.Knock-down CapG in PASMCs resulted in decreased proliferation, increased apoptosis and induced cell cycle inhibition. Down-regulation of CapG expression locally could attenuate pulmonary hypertension, pulmonary vascular remodeling and right ventricular hypertrophy in HPH rat model.Our study indicated that CapG participated in the pathogenesis of pulmonary vascular remodeling in HPH rats, which was probably mediated by promoting the proliferation and inhibiting the apoptosis of PASMCs. We proposed CapG modulating protective effects of pulmonary hypertension.
科研通智能强力驱动
Strongly Powered by AbleSci AI