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首页> 外文期刊>Journal of cell biology >A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility
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A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility

机译:NUMB–EFA6B–ARF6的回收途径可控制顶端受限制的细胞突起和间充质运动

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摘要

The endocytic protein NUMB has been implicated in the control of various polarized cellular processes, including the acquisition of mesenchymal migratory traits through molecular mechanisms that have only been partially defined. Here, we report that NUMB is a negative regulator of a specialized set of understudied, apically restricted, actin-based protrusions, the circular dorsal ruffles (CDRs), induced by either PDGF or HGF stimulation. Through its PTB domain, NUMB binds directly to an N-terminal NPLF motif of the ARF6 guanine nucleotide exchange factor, EFA6B, and promotes its exchange activity in vitro. In cells, a NUMB–EFA6B–ARF6 axis regulates the recycling of the actin regulatory cargo RAC1 and is critical for the formation of CDRs that mark the acquisition of a mesenchymal mode of motility. Consistently, loss of NUMB promotes HGF-induced cell migration and invasion. Thus, NUMB negatively controls membrane protrusions and the acquisition of mesenchymal migratory traits by modulating EFA6B–ARF6 activity.
机译:内吞蛋白NUMB与各种极化细胞过程的控制有关,包括通过仅部分定义的分子机制获得间充质迁移性状。在这里,我们报告NUMB是由PDGF或HGF刺激引起的一组专门研究的,研究不足的,根尖受限制的,基于肌动蛋白的突起,圆形背褶(CDR)的负调节剂。通过其PTB结构域,NUMB直接与ARF6鸟嘌呤核苷酸交换因子EFA6B的N端NPLF基序结合,并在体外促进其交换活性。在细胞中,NUMB–EFA6B–ARF6轴可调节肌动蛋白调节货物RAC1的回收利用,并且对于形成CDR的形成至关重要,而CDR则标志着间充质运动模式的获得。一致地,NUMB的丢失促进了HGF诱导的细胞迁移和侵袭。因此,NUMB通过调节EFA6B–ARF6活性来负面地控制膜突出和间充质迁徙性状的获得。

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