在共培养系统中,剪切应力对血管平滑肌细胞迁移的内皮调节起保护作用。

Han Qin Wang, Lang Xian Huang, Ming Juan Qu, Zhi Qiang Yan, Bo Liu, Bao Rong Shen, Zong Lai Jiang
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引用次数: 53

摘要

血管内皮细胞(ECs)不断暴露于血流诱导的剪切应力;这些力强烈影响邻近血管平滑肌细胞(VSMCs)的行为。VSMC的迁移是血管壁重构的关键事件。在这项研究中,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室系统和Transwell迁移实验,他们证明在静态条件下,人类内皮细胞与VSMC共培养诱导了VSMC迁移,而在EC侧施加12小时的层流剪切应力(1.5 Pa, 15 dynes/cm2)显著抑制了这一过程。VSMC迁移的变化主要依赖于ec和VSMC之间的密切相互作用。Western blotting结果显示,Akt磷酸化水平与剪应力介导的EC调控VSMC迁移的效果之间存在一致的相关性。Wortmannin和Akti显著抑制ec诱导的VSMC Akt磷酸化和迁移作用。这些结果表明,剪切应力可以阻止内皮细胞对VSMC迁移的调节,这可能是血管壁的一种动脉粥样硬化保护功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shear stress protects against endothelial regulation of vascular smooth muscle cell migration in a coculture system.

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.

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