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FRET biosensor allows spatio-temporal observation of shear stress-induced polar RhoGDIα activation

机译:FRET生物传感器允许时空观察剪切应力诱导的极性RhoGDIα激活

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摘要

Rho GDP-dissociation inhibitor α (RhoGDIα) is a known negative regulator of the Rho family that shuts off GDP/GTP cycling and cytoplasm/membrane translocation to regulate cell migration. However, to our knowledge, no reports are available that focus on how the RhoGDIα-Rho GTPases complex is activated by laminar flow through exploring the activation of RhoGDIα itself. Here, we constructed a new biosensor using fluorescence resonance energy transfer (FRET) technology to measure the spatio-temporal activation of RhoGDIα in its binding with Rho GTPases in living HeLa cells. Using this biosensor, we find that the dissociation of the RhoGDIα-Rho GTPases complex is increased by shear stress, and its dissociation rate varies with subcellular location. Moreover, this process is mediated by membrane fluidity, cytoskeleton and Src activity, which indicates that the regulation of RhoGDIα activation under shear stress application represents a relatively separate pathway from the shear stress-induced Rho pathway.
机译:Rho GDP离解抑制剂α(RhoGDIα)是Rho家族的已知负调节剂,它可以关闭GDP / GTP循环和细胞质/膜移位来调节细胞迁移。然而,据我们所知,尚无报道关注通过研究RhoGDIα本身的活化如何通过层流活化RhoGDIα-RhoGTPases复合物。在这里,我们使用荧光共振能量转移(FRET)技术构造了一种新型生物传感器,以测量RhoGDIα与活HeLa细胞中Rho GTPases结合时的时空激活。使用该生物传感器,我们发现RhoGDIα-RhoGTPases复合物的解离通过剪切应力而增加,并且其解离速率随亚细胞位置而变化。而且,该过程由膜流动性,细胞骨架和Src活性介导,这表明在施加剪切应力下RhoGDIα活化的调节代表了与剪切应力诱导的Rho途径相对独立的途径。

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