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The Rac activator STEF (Tiam2) regulates cell migration by microtubule-mediated focal adhesion disassembly

机译:Rac激活剂STEF(Tiam2)通过微管介导的粘着斑拆卸来调节细胞迁移

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摘要

Focal adhesion (FA) disassembly required for optimal cell migration is mediated by microtubules (MTs); targeting of FAs by MTs coincides with their disassembly. Regrowth of MTs, induced by removal of the MT destabilizer nocodazole, activates the Rho-like GTPase Rac, concomitant with FA disassembly. Here, we show that the Rac guanine nucleotide exchange factor (GEF) Sif and Tiam1-like exchange factor (STEF) is responsible for Rac activation during MT regrowth. Importantly, STEF is required for multiple targeting of FAs by MTs. As a result, FAs in STEF-knockdown cells have a reduced disassembly rate and are consequently enlarged. This leads to reduced speed of migration. Together, these findings suggest a new role for STEF in FA disassembly and cell migration through MT-mediated mechanisms.
机译:最佳细胞迁移所需的粘着性粘附(FA)拆卸是由微管(MTs)介导的。 MT对FA的定位恰好与它们的拆卸相吻合。通过去除MT稳定剂诺考达唑诱导MT的再生,激活了Rho样GTPase Rac,并伴随FA的分解。在这里,我们显示Rac鸟嘌呤核苷酸交换因子(GEF)Sif和Tiam1样交换因子(STEF)负责MT再生期间的Rac激活。重要的是,MT必须将STEF用作FA的多重目标。结果,STEF组合式细胞中的FA分解率降低,因此扩大。这导致迁移速度降低。在一起,这些发现表明STEF通过MT介导的机制在FA拆卸和细胞迁移中具有新的作用。

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