Yu Muqing, Liu Xiansheng, Wu Hongxu, Ni Wang, Chen Shixin, Xu Yongjian
Department of Respiratory and Critical Care Medicine, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, P.R. China.
Exp Ther Med. 2017 Nov;14(5):4671-4680. doi: 10.3892/etm.2017.5160. Epub 2017 Sep 21.
Cigarette smoke may contribute to pulmonary vascular remodeling (PVR), a result of the proliferation of pulmonary artery smooth muscle cells (PASMCs), before pulmonary hypertension in chronic obstructive pulmonary disease (COPD). Activated extracellular signal-regulated kinases 1 and 2 (ERK1/2) are considered to be involved the process of PVR. This study investigated the potential role of ERK1/2 in the proliferation of rat PASMCs (rPASMCs) and cigarette smoke-induced PVR in rats. A small interfering RNA (siRNA) against ERK1/2 (ERK1/2-siRNA) was synthesized, and it significantly reduced the expression of ERK1/2 and cyclin E1, significantly increased the proportion of cells arrested at G0/G1 phase and significantly suppressed the proliferation of rPASMCs treated with cigarette smoke extract compared with controls (all P<0.05). In rats, ERK1/2-siRNA, which was administered intranasally, also inhibited the activation of ERK1/2 and the upregulation of cyclin E1, both of which were induced after the rats were exposed to cigarette smoke for 3 months. ERK1/2-siRNA also significantly reduced PVR (observed by vessel wall thickness and the proportion of fully muscularized vessels) in cigarette smoke-exposed rats compared with a negative control siRNA (P<0.05). Collectively, these data indicated that ERK1/2-siRNA could attenuate PVR in cigarette smoke-exposed rats, and it may have therapeutic value in the treatment of COPD.
香烟烟雾可能会导致肺血管重塑(PVR),这是慢性阻塞性肺疾病(COPD)患者在发生肺动脉高压之前肺动脉平滑肌细胞(PASMCs)增殖的结果。活化的细胞外信号调节激酶1和2(ERK1/2)被认为参与了PVR的过程。本研究调查了ERK1/2在大鼠PASMCs(rPASMCs)增殖以及香烟烟雾诱导的大鼠PVR中的潜在作用。合成了针对ERK1/2的小干扰RNA(siRNA)(ERK1/2-siRNA),与对照组相比,它显著降低了ERK1/2和细胞周期蛋白E1的表达,显著增加了停滞在G0/G1期的细胞比例,并显著抑制了经香烟烟雾提取物处理的rPASMCs的增殖(所有P<0.05)。在大鼠中,经鼻给予的ERK1/2-siRNA也抑制了ERK1/2的激活和细胞周期蛋白E1的上调,这两者都是在大鼠暴露于香烟烟雾3个月后诱导产生的。与阴性对照siRNA相比,ERK1/2-siRNA还显著降低了暴露于香烟烟雾的大鼠的PVR(通过血管壁厚度和完全肌化血管的比例观察)(P<0.05)。总体而言,这些数据表明ERK1/2-siRNA可以减轻暴露于香烟烟雾的大鼠的PVR,并且它可能在COPD的治疗中具有治疗价值。