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首页> 外文期刊>Nature cell biology >Feedback regulation between plasma membrane tension and membrane-bending proteins organizes cell polarity during leading edge formation
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Feedback regulation between plasma membrane tension and membrane-bending proteins organizes cell polarity during leading edge formation

机译:质膜张力和膜弯曲蛋白之间的反馈调节在前沿形成过程中组织细胞极性

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摘要

Tension applied to the plasma membrane (PM) is a global mechanical parameter involved in cell migration. However, how membrane tension regulates actin assembly is unknown. Here, we demonstrate that FBP17, a membrane-bending protein and an activator of WASP/N-WASP-dependent actin nucleation, is a PM tension sensor involved in leading edge formation. In migrating cells, FBP17 localizes to short membrane invaginations at the leading edge, while diminishing from the cell rear in response to PM tension increase. Conversely, following reduced PM tension, FBP17 dots randomly distribute throughout the cell, correlating with loss of polarized actin assembly on PM tension reduction. Actin protrusive force is required for the polarized accumulation, indicating a role for FBP17-mediated activation of WASP/N-WASP in PM tension generation. In vitro experiments show that FBP17 membrane-bending activity depends on liposomal membrane tension. Thus, FBP17 is the local activator of actin polymerization that is inhibited by PM tension in the feedback loop that regulates cell migration.
机译:施加于质膜(PM)的张力是细胞迁移所涉及的全局机械参数。然而,膜张力如何调节肌动蛋白组装尚不清楚。在这里,我们证明FBP17,膜弯曲蛋白和WASP / N-WASP依赖性肌动蛋白成核的激活剂,是参与前缘形成的PM张力传感器。在迁移的细胞中,FBP17定位在前缘的短膜内陷处,同时随着PM张力的增加而从细胞后部减少。相反,在降低PM张力后,FBP17点随机分布在整个细胞中,这与极化肌动蛋白装配在PM张力降低时的损失有关。极化积累需要肌动蛋白突出力,表明FBP17介导的WASP / N-WASP激活在PM张力产生中的作用。体外实验表明,FBP17膜弯曲活性取决于脂质体膜张力。因此,FBP17是肌动蛋白聚合反应的局部活化剂,它受到调节细胞迁移的反馈回路中PM张力的抑制。

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