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Effect of Initial Orientation of Vascular Endothelial Cells on Activation of RhoGTPases Induced by Fluid Shear Stress

机译:血管内皮细胞初始取向对流体剪切应力诱导的RhoGTP酶激活的影响

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Vascular endothelial cells (ECs) exposed to fluid shear stress (FSS) become elongated and aligned to the direction of flow. However, the process of morphological change in individual cells is different depending of their initial shape. Rac1 and RhoA, members of the family of Rho GTPases, play important roles in cellular morphological changes but are thought to be activated differently in the process. Here, we measured changes in Rac1 and RhoA activities with a focus on the effect of cell orientation when exposed to FSS. In ECs initially oriented parallel to the direction of flow, RhoA and Rac1 were activated primarily in the upstream and the downstream regions of cells, respectively, accompanied by the formation of lamellipodia in the direction of flow. On the other hand, in cells oriented perpendicular to the direction of flow, FSS caused RhoA activation in the upstream region but did not change Rac1 activity. Furthermore, treatment with cytochalasin D inhibited the localization of Rac1 activation and suppressed RhoA activation by FSS. These results indicate that cell orientation affects the local activation of Rac1 and RhoA when induced by forces transmitted through the actin cytoskeleton under a FSS condition.
机译:暴露于流体剪切应力(FSS)的血管内皮细胞(EC)变得细长并与流动方向对齐。但是,单个细胞的形态变化过程取决于它们的初始形状。 Rac1和RhoA,Rho GTPases家族的成员,在细胞形态变化中起重要作用,但在此过程中被激活的方式有所不同。在这里,我们测量了Rac1和RhoA活性的变化,重点是暴露于FSS时细胞方向的影响。在最初平行于流动方向定向的EC中,RhoA和Rac1主要分别在细胞的上游和下游区域被激活,并在流动方向上形成了片状脂膜。另一方面,在垂直于流动方向定向的细胞中,FSS在上游区域引起RhoA激活,但未改变Rac1活性。此外,用细胞松弛素D抑制Rac1激活的本地化,并抑制FSS的RhoA激活。这些结果表明,在FSS条件下,通过肌动蛋白细胞骨架传递的力诱导细胞定向会影响Rac1和RhoA的局部激活。

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