4.7 Article

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

期刊

EMBO REPORTS
卷 11, 期 4, 页码 292-298

出版社

WILEY
DOI: 10.1038/embor.2010.10

关键词

focal adhesions; microtubules; Rac; STEF; Tiam2

资金

  1. Bioimaging Facility of the Faculty of Life Sciences (The University of Manchester)
  2. Biotechnology and Biological Sciences Research Council [BB/G004552/1]
  3. Cancer Research UK [C147/A6058]
  4. BBSRC [BB/G004552/1] Funding Source: UKRI
  5. Biotechnology and Biological Sciences Research Council [BB/G004552/1] Funding Source: researchfish

向作者/读者索取更多资源

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.

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