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Directing Vascular Cell Selectivity and Hemocompatibility on Patterned Platforms Featuring Variable Topographic Geometry and Size

机译:在具有可变拓扑几何形状和大小的图案化平台上指导血管细胞选择性和血液相容性

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摘要

It is great challenge to generate multifunctionality of vascular grafts and stents to enable vascular cell selectivity and improve hemocompatibility. Microanopatterning of vascular implant surfaces for such multi-functionality is a direction to be explored. We developed a novel patterned platform featuring two typical geometries (groove and pillar) and six pattern sizes (0.5—50 μm) in a single substrate to evaluate the response of vascular cells and platelets. Our results indicate that targeted multifunctionality can be indeed instructed by rationally designed surface topography. The pillars nonselectively inhibited the growth of endothelial and smooth muscle cells. By contrast, the grooves displayed selective effects: in a size-dependent manner, the grooves enhanced endothelialization but inhibited the growth of smooth muscle cells. Moreover, our studies suggest that topographic cues can affect response of vascular cells by regulating focal adhesion and stress fiber development, which define cytoskeleton organization and cell shape. Notably, both the grooves and the pillars at 1 μm size drastically reduced platelet adhesion and activation. Taken together, these findings suggest that the topographic pattern featuring 1 μm grooves may be the optimal design of surface multifunctionality that favors vascular cell selectivity and improves hemocompatibility.
机译:产生血管移植物和支架的多功能性以实现血管细胞选择性和改善血液相容性是一个巨大的挑战。对于这样的多功能性,血管植入物表面的微/纳米成像是一个需要探索的方向。我们开发了一种新颖的图案化平台,该平台在单个基板上具有两种典型的几何形状(凹槽和支柱)和六种图案尺寸(0.5-50μm),以评估血管细胞和血小板的反应。我们的结果表明,可以通过合理设计的表面形貌确实指导目标多功能。支柱非选择性地抑制内皮细胞和平滑肌细胞的生长。相比之下,凹槽显示出选择性的效果:以尺寸依赖的方式,凹槽增强了内皮化作用,但抑制了平滑肌细胞的生长。此外,我们的研究表明,地形线索可以通过调节粘着斑和应力纤维的发育来影响血管细胞的反应,这决定了细胞骨架的组织和细胞的形状。值得注意的是,尺寸为1μm的凹槽和柱子都大大降低了血小板的附着力和活化。综上所述,这些发现表明,具有1μm凹槽的地形图可能是表面多功能性的最佳设计,有利于血管细胞选择性并改善血液相容性。

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