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整合素-FAK-Rho GTPases 通路在血管内皮细胞感知和响应等离子体纳米涂层表面润湿性中的作用。

Integrins-FAK-Rho GTPases pathway in endothelial cells sense and response to surface wettability of plasma nanocoatings.

机构信息

Institute of Biomedical Engineering, School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.

出版信息

ACS Appl Mater Interfaces. 2013 Jun 12;5(11):5112-21. doi: 10.1021/am400973a. Epub 2013 May 15.

Abstract

Vascular endothelial cell (EC) adhesion and migration are essential processes in re-endothelialization of implanted biomaterials, which are affected by surface properties of implanted materials such as surface wettability. Our previous study demonstrated that, as model substrates, EC adhesion/migration showed an opposite behavior on the hydrophobic and hydrophilic surfaces of plasma SiOx:H nanocoatings. Extending our previous works, the expression and distribution of crucial proteins in integrins-FAK-Rho GTPases signaling pathways were examined, respectively. The results showed that a hydrophilic surface could enhance the expression of focal adhesion protein associated with cell adhesion; however, the hydrophobic surface could improve the expression of Rho GTPases associated with cell migration and phosphorylation level of FAK, revealing the potential reason of surface wettability mediating different cells' adhesion/migration behaviors. These findings reveal the relationship and molecular mechanism of endothelial cell adhesion/migration, which was expected to guide the surface modification of implants for accelerating endothelialization.

摘要

血管内皮细胞(EC)黏附和迁移是植入生物材料再内皮化的必要过程,其受到植入材料表面特性的影响,如表面润湿性。我们之前的研究表明,作为模型底物,EC 在等离子体 SiOx:H 纳米涂层的疏水和亲水表面上表现出相反的黏附/迁移行为。在我们之前工作的基础上,进一步研究了整合素-FAK-Rho GTPases 信号通路中关键蛋白的表达和分布。结果表明,亲水表面可以增强与细胞黏附相关的黏着斑蛋白的表达;然而,疏水表面可以提高与细胞迁移相关的 Rho GTPases 以及 FAK 的磷酸化水平,揭示了表面润湿性调节不同细胞黏附/迁移行为的潜在原因。这些发现揭示了内皮细胞黏附和迁移的关系和分子机制,有望指导植入物表面改性以加速内皮化。

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