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Directional shear flow and Rho activation prevent the endothelial cell apoptosis induced by micropatterned anisotropic geometry

机译:定向剪切流和Rho激活可防止微图案各向异性几何体诱导的内皮细胞凋亡

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摘要

To study the roles of anisotropic cell morphology and directionality of mechanical force in apoptosis, the spreading of human umbilical vein endothelial cells (HUVECs) was constrained by growing on micropatterned (MP) strips of fibronectin (FN, 20 μg/cm2) with widths of 15, 30, and 60 μm on silicone membrane. Cells on 30- and 60-μm strips, like cells on a nonpatterned (NP) surface coated with FN, showed clear actin stress fibers with anchoring spots of phosphorylated focal adhesion kinase (p-FAK) and no significant apoptosis. On 15-μm strips, cells had few stress fibers, no p-FAK, and significant apoptosis. After seeding for 12 h, the cells were subjected to pulsatile shear stress (12 ± 4 dyn/cm2) parallel or perpendicular to MP strips, or kept under static condition. Parallel flow caused cell elongation with enhanced stress fibers and p-FAK, and a reduction in apoptosis, but perpendicular flow did not. The Rho inhibitory C3 exoenzyme abolished the effects of parallel flow. RhoV14, the constitutively active Rho, enhanced stress fibers and p-FAK, and prevented apoptosis of HUVECs on 15-μm strips under static condition. RhoV14 also reduced cell apoptosis under both parallel and perpendicular flows. Our results indicate that cell apoptosis can be modulated by changes in ECM micropatterning, anisotropic cell morphology, and mechanical forces. These extracellular microenvironment factors affect cell survival through alterations in Rho GTPase activity, stress fiber organization, and FAK phosphorylation.
机译:为了研究各向异性细胞形态和机械力的方向性在凋亡中的作用,通过在纤连蛋白的微图案(MP)条(FN,20μg/ cm 2)上生长来限制人脐静脉内皮细胞(HUVEC)的扩散)在硅胶膜上的宽度为15、30和60μm。 30和60μm条带上的细胞,像涂有FN的无图案(NP)表面上的细胞一样,显示出清晰的肌动蛋白应激纤维,带有磷酸化粘着斑激酶(p-FAK)的锚定点,并且没有明显的凋亡。在15μm的条带上,细胞几乎没有应力纤维,没有p-FAK,并且凋亡明显。接种12小时后,使细胞经受平行于或垂直于MP条的脉动剪切应力(12±4 dyn / cm 2 ),或保持在静态条件下。平行流动引起细胞伸长,其中应力纤维和p-FAK增强,凋亡减少,但垂直流动却没有。 Rho抑制性C3外酶消除了平行流的影响。 RhoV14(一种具有活性的Rho)增强了应力纤维和p-FAK,并在静态条件下阻止了15μm条带上HUVEC的凋亡。 RhoV14还减少了平行和垂直流动下的细胞凋亡。我们的结果表明,细胞凋亡可以通过ECM显微图案,各向异性细胞形态和机械力的变化来调节。这些细胞外微环境因素通过Rho GTPase活性,应激纤维组织和FAK磷酸化改变影响细胞存活。

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