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CCM proteins control endothelial β1 integrin dependent response to shear stress

机译:CCM蛋白控制内皮β1整合素对剪切应力的依赖性反应

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Hemodynamic shear stress from blood flow on the endothelium critically regulates vascular function in many physiological and pathological situations. Endothelial cells adapt to shear stress by remodeling their cytoskeletal components and subsequently by changing their shape and orientation. We demonstrate that β1 integrin activation is critically controlled during the mechanoresponse of endothelial cells to shear stress. Indeed, we show that overexpression of the CCM complex, an inhibitor of β1 integrin activation, blocks endothelial actin rearrangement and cell reorientation in response to shear stress similarly to β1 integrin silencing. Conversely, depletion of CCM2 protein leads to an elongated “shear-stress-like” phenotype even in the absence of flow. Taken together, our findings reveal the existence of a balance between positive extracellular and negative intracellular signals, i.e. shear stress and CCM complex, for the control of β1 integrin activation and subsequent adaptation of vascular endothelial cells to mechanostimulation by fluid shear stress.
机译:在许多生理和病理情况下,来自内皮上血流的血液动力剪切应力可严格调节血管功能。内皮细胞通过重塑细胞骨架成分并随后改变其​​形状和方向来适应剪切应力。我们证明,在内皮细胞对切应力的机械反应过程中,β1整合素的激活受到严格控制。确实,我们证明了CCM复合物(β1整合素激活的抑制剂)的过表达与β1整合素沉默类似,可响应剪切应力而阻止内皮肌动蛋白重排和细胞重新定向。相反,即使没有血流,CCM2蛋白的消耗也会导致延长的“剪切应力样”表型。综上所述,我们的发现揭示了细胞外正信号和细胞内负信号之间的平衡,即剪切应力和CCM复合物之间的平衡,用于控制β1整联蛋白的活化以及随后血管内皮细胞通过流体剪切应力适应机械刺激。

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