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Regulation of leading edge microtubule and actin dynamics downstream of Rac1
被引:219
作者:
Wittmann, T
Bokoch, GM
Waterman-Storer, CM
机构:
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Inst Childhood & Neglected Dis, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词:
cell motility;
cytoskeleton;
tubulin;
Rho GTPases;
p21-activated;
kinase;
D O I:
10.1083/jcb.200303082
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Actin in migrating cells is regulated by Rho GTPases. However, Rho proteins might also affect microtubules (MTs). Here, we used time-lapse microscopy of PtK1 cells to examine MT regulation downstream of Rac1. In these cells, "pioneer" MTs growing into leading-edge protrusions exhibited a decreased catastrophe frequency and an increased time in growth as compared with MTs further from the leading edge. Constitutively active Rac1(Q61L) promoted pioneer behavior in most MTs, whereas dominant-negative Rac1(T17N) eliminated pioneer MTs, indicating that Rac1 is a regulator of MT dynamics in vivo. Rac1(Q61L) also enhanced MT turnover through stimulation of MT retrograde flow and breakage. Inhibition of p21-activated kinases (Paks), downstream effectors of Rac1, inhibited Rac1 (Q61L)-induced MT growth and retrograde flow. In addition, Rac1 (Q61L) promoted lamellipodial actin polymerization and Pak-dependent retrograde flow. Together, these results indicate coordinated regulation of the two cytoskeletal systems in the leading edge of migrating cells.
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页码:845 / 851
页数:7
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