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Microtubules regulate GEF-H1 in response to extracellular matrix stiffness

机译:微管调节GEF-H1以响应细胞外基质的硬度

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Breast epithelial cells sense the stiffness of the extracellular matrix through Rho-mediated contractility. In turn, matrix stiffness regulates RhoA activity. However, the upstream signaling mechanisms are poorly defined. Here we demonstrate that the Rho exchange factor GEF-H1 mediates RhoA activation in response to extracellular matrix stiffness. We demonstrate the novel finding that microtubule stability is diminished by a stiff three-dimensional (3D) extracellular matrix, which leads to the activation of GEF-H1. Surprisingly, activation of the mitogen-activated protein kinase kinase/extracellular signal-regulated kinase pathway did not contribute to stiffness-induced GEF-H1 activation. Loss of GEF-H1 decreases cell contraction of and invasion through 3D matrices. These data support a model in which matrix stiffness regulates RhoA through microtubule destabilization and the subsequent release and activation of GEF-H1.
机译:乳房上皮细胞通过Rho介导的收缩力来感知细胞外基质的硬度。反过来,基质刚度调节RhoA活性。但是,上游信令机制定义不清。在这里,我们证明了Rho交换因子GEF-H1介导了RhoA激活以响应细胞外基质的硬度。我们证明了新颖的发现,即微管的稳定性被刚性的三维(3D)细胞外基质所削弱,从而导致GEF-H1的激活。出人意料的是,丝裂原活化的蛋白激酶激酶/细胞外信号调节激酶途径的活化并没有促进僵硬性诱导的GEF-H1活化。 GEF-H1的丢失减少了3D基质的细胞收缩和侵袭。这些数据支持了一个模型,其中基质刚度通过微管去稳定以及随后的GEF-H1释放和激活来调节RhoA。

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