Cdc42 and Vesicle Trafficking in Polarized Cells

被引:142
作者
Harris, Kathryn P. [1 ]
Tepass, Ulrich [1 ]
机构
[1] Univ Toronto, Dept Cell Syst Biol, Toronto, ON M5S 3G5, Canada
关键词
adherens junctions; aPKC; Arp2; 3; Cdc42; cell polarity; Drosophila; Par3; Par6; vesicle trafficking; yeast; EPITHELIAL MORPHOGENESIS; SACCHAROMYCES-CEREVISIAE; INTERCELLULAR-JUNCTIONS; DYNAMIC LOCALIZATION; ACTIN POLYMERIZATION; ADHERENS JUNCTIONS; GOLGI MEMBRANES; PAR PROTEINS; N-WASP; ENDOCYTOSIS;
D O I
10.1111/j.1600-0854.2010.01102.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cdc42, a highly conserved small GTPase of the Rho family, acts as a molecular switch to modulate a wide range of signaling pathways. Vesicle trafficking and cell polarity are two processes Cdc42 is known to regulate. Although the trafficking and polarity machineries are each well understood, how they interact to cross-regulate each other in cell polarization is still a mystery. Cdc42 is an interesting candidate that may integrate these two networks within the cell. Here we review findings on the interplay between Cdc42 and trafficking in yeast, Caenorhabditis elegans, Drosophila and mammalian cell culture systems, and discuss recent advances in our understanding of the function of Cdc42 and two of its effectors, the WASp-Arp2/3 and Par complexes, in regulating polarized traffic. Work in yeast suggests that the polarized distribution of Cdc42, which acts here as a key polarity determinant, requires input from multiple processes including endocytosis and recycling. In metazoan cells, Cdc42 can regulate several steps in the biosynthetic as well as endocytotic and recycling pathways. The recent discovery that the Par polarity complex co-operates with Cdc42 in the regulation of endocytosis and recycling opens exciting possibilities for the integration of polarity protein function and endocytotic machinery.
引用
收藏
页码:1272 / 1279
页数:8
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