Li Zhen-Xing, Luo Ya-Ling, Xu Jian, Ren Dun-Qiang, Zhao Yan-Xia
Department of Respiratory Diseases, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2008 Jun;28(6):1031-4.
To investigate the role of Rho-kinase signaling pathway in human airway smooth muscle cell (ASMCs) migration and cytoskeletal reorganization induced by endothelin-1 (ET-1).
Primary cultured human ASMCs obtained by tracheal explant culture method were examined for cell migration in response to ET-1 treatment using modified Boyden chambers. The changes in actin cytoskeletal reorganization were observed under confocal laser scanning microscope, and the phosphorylation of myosin-phosphatase target 1 (p-MYPT1) was examined using Western blot analysis.
At the concentration of 0.1, 1, 10, and 100 nmol/L, ET-1 induced migration of the ASMCs, and 10 nmol/L ET-1 produced the most obvious effect (P<0.01). Rho-kinase inhibitor Y-27632 showed a dose-dependent inhibitory effect on ET-1-induced ASMC migration, and in cells exposed to 10 nmol/L ET-1, Y-27632 at 10 micromol/L significantly blocked ASMC migration (P<0.01). ET-1 (10 nmol/L) exposure resulted in reorganization of actin cytoskeleton and formation of stress fibers in the ASMCs, which were obviously inhibited by Y-27632. Compared with the control group, the AMSCs showed significant enhancement of p-MYPT1 protein expression after ET-1 exposure for 15 and 30 min (P<0.01), but prolonged exposure failed to result in the expression enhancement (P>0.05).
Rho-kinase signaling pathway may play an important role in ET-1-induced ASMC migration and reorganization of actin cytoskeleton.
探讨Rho激酶信号通路在内皮素-1(ET-1)诱导的人气道平滑肌细胞(ASMCs)迁移和细胞骨架重组中的作用。
采用气管外植体培养法获得原代培养的人ASMCs,使用改良的Boyden小室检测ET-1处理后细胞的迁移情况。在共聚焦激光扫描显微镜下观察肌动蛋白细胞骨架重组的变化,并用蛋白质印迹分析检测肌球蛋白磷酸酶靶标1(p-MYPT1)的磷酸化情况。
在0.1、1、10和100 nmol/L浓度下,ET-1诱导ASMCs迁移,10 nmol/L ET-1的作用最为明显(P<0.01)。Rho激酶抑制剂Y-27632对ET-1诱导的ASMC迁移呈剂量依赖性抑制作用,在暴露于10 nmol/L ET-1的细胞中,10 μmol/L的Y-27632显著阻断ASMC迁移(P<0.01)。暴露于10 nmol/L ET-1导致ASMCs中肌动蛋白细胞骨架重组和应力纤维形成,这被Y-27632明显抑制。与对照组相比,ET-1暴露15和30分钟后,ASMCs的p-MYPT1蛋白表达显著增强(P<0.01),但延长暴露时间未导致表达增强(P>0.05)。
Rho激酶信号通路可能在ET-1诱导的ASMC迁移和肌动蛋白细胞骨架重组中起重要作用。