Wang Han Qin, Huang Lang Xian, Qu Ming Juan, Yan Zhi Qiang, Liu Bo, Shen Bao Rong, Jiang Zong Lai
School of Life Sciences and Biotechnology, Institute of Mechanobiology and Medical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Endothelium. 2006 May-Jun;13(3):171-80. doi: 10.1080/10623320600760282.
Vascular endothelial cells (ECs) are constantly exposed to blood flow-induced shear stress; these forces strongly influence the behaviors of neighboring vascular smooth muscle cells (VSMCs). VSMC migration is a key event in vascular wall remodeling. In this study, the authors assessed the difference between VSMC migration in VSMC/EC coculture under static and shear stress conditions. Utilizing a parallel-plate coculture flow chamber system and Transwell migration assays, they demonstrated that human ECs cocultured with VSMCs under static conditions induced VSMC migration, whereas laminar shear stress (1.5 Pa, 15 dynes/cm2) applied to the EC side for 12 h significantly inhibited this process. The changes in VSMC migration is mainly dependent on the close interactions between ECs and VSMCs. Western blotting showed that there was a consistent correlation between the level of Akt phosphorylation and the efficacy of shear stress-mediated EC regulation of VSMC migration. Wortmannin and Akti significantly inhibited the EC-induced effect on VSMC Akt phosphorylation and migration. These results indicate that shear stress protects against endothelial regulation of VSMC migration, which may be an atheroprotective function on the vessel wall.
血管内皮细胞(ECs)持续暴露于血流诱导的剪切应力下;这些力强烈影响相邻血管平滑肌细胞(VSMCs)的行为。VSMC迁移是血管壁重塑中的关键事件。在本研究中,作者评估了静态和剪切应力条件下VSMC/EC共培养中VSMC迁移的差异。利用平行板共培养流动腔系统和Transwell迁移试验,他们证明,在静态条件下与VSMCs共培养的人ECs可诱导VSMC迁移,而在EC侧施加12小时的层流剪切应力(1.5 Pa,15达因/平方厘米)可显著抑制这一过程。VSMC迁移的变化主要取决于ECs与VSMCs之间的紧密相互作用。蛋白质印迹法显示,Akt磷酸化水平与剪切应力介导的EC对VSMC迁移的调节功效之间存在一致的相关性。渥曼青霉素和Akti显著抑制了EC诱导的对VSMC Akt磷酸化和迁移的影响。这些结果表明,剪切应力可防止内皮对VSMC迁移的调节,这可能是血管壁上的一种抗动脉粥样硬化功能。