Regulation of leading edge microtubule and actin dynamics downstream of Rac1

J Cell Biol. 2003 Jun 9;161(5):845-51. doi: 10.1083/jcb.200303082.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actin Cytoskeleton / metabolism*
  • Animals
  • Cell Movement / physiology*
  • Cell Polarity / physiology*
  • Cells, Cultured
  • Enzyme Inhibitors / pharmacology
  • Eukaryotic Cells / metabolism*
  • Microscopy, Video
  • Microtubules / metabolism*
  • Mutation / genetics
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / metabolism
  • Pseudopodia / metabolism*
  • p21-Activated Kinases
  • rac1 GTP-Binding Protein / genetics
  • rac1 GTP-Binding Protein / metabolism*

Substances

  • Enzyme Inhibitors
  • Protein Serine-Threonine Kinases
  • p21-Activated Kinases
  • rac1 GTP-Binding Protein