Arf6 and microtubules in adhesion-dependent trafficking of lipid rafts

被引:163
作者
Balasubramanian, Nagaraj
Scott, David W.
Castle, J. David
Casanova, James E.
Schwartz, Martin Alexander [1 ]
机构
[1] Univ Virginia, Mellon Prostate Canc Res Inst, Robert M Beirne Cardiovasc Res Ctr, Charlottesville, VA 22908 USA
[2] Univ Virginia, Mellon Prostate Canc Res Inst, Dept Cell Biol, Charlottesville, VA 22908 USA
[3] Univ Virginia, Mellon Prostate Canc Res Inst, Dept Microbiol, Charlottesville, VA 22908 USA
[4] Univ Virginia, Mellon Prostate Canc Res Inst, Dept Biomed Engn, Charlottesville, VA 22908 USA
关键词
D O I
10.1038/ncb1657
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Integrin-mediated adhesion regulates membrane binding sites for Rac1 within lipid rafts. Detachment of cells from the substratum triggers the clearance of rafts from the plasma membrane through caveolin-dependent internalization. The small GTPase Arf6 and microtubules also regulate Rac-dependent cell spreading and migration, but the mechanisms are poorly understood. Here we show that endocytosis of rafts after detachment requires F-actin, followed by microtubule-dependent trafficking to recycling endosomes. When cells are replated on fibronectin, rafts exit from recycling endosomes in an Arf6-dependent manner and return to the plasma membrane along microtubules. Both of these steps are required for the plasma membrane targeting of Rac1 and for its activation. These data therefore define a new membrane raft trafficking pathway that is crucial for anchorage-dependent signalling.
引用
收藏
页码:1381 / U73
页数:18
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