Parallel phosphatidylinositol 3-kinase (PI3K)-dependent and Src-dependent pathways lead to CXCL8-mediated Rac2 activation and chemotaxis

J Biol Chem. 2008 Sep 26;283(39):26538-47. doi: 10.1074/jbc.M805611200. Epub 2008 Jul 28.

Abstract

The requirement for phosphatidylinositol 3-kinase (PI3K) in the establishment of cell polarity and motility in a number of cell types has recently come into question. In this study, we demonstrate that inhibition of PI3K by wortmannin in neutrophil-like differentiated HL60 cells expressing CXCR2 resulted in reduced cell motility but normal chemotaxis in response to a gradient of CXCL8. However, wortmannin inhibition of PI3K did impair the ability of cells to re-orient their polarity and respond quickly to a change in the direction of the CXCL8 gradient. We hypothesized that Src-regulated ELMO-Dock2-Rac2 activation mediates chemotaxis in the absence of PI3K activity. Inhibition of Src with the small molecule inhibitor, PP2, or inhibition of Dock2 by shRNA knockdown confirmed the functional role of Src and Dock2 in regulating chemotaxis when PI3K was inhibited. Moreover, neutrophils isolated from bone marrow of hck(-/-)fgr(-/-)lyn(-/-) mice exhibited much more severe inhibition of chemotaxis when PI3K was blocked with wortmannin as compared with neutrophils isolated from bone marrow of wild-type mice. Thus, PI3K and Src-ELMO-Dock2 pathways work in parallel to activate Rac2 and modulate chemotaxis in response to a CXCL8 gradient in neutrophils.

Publication types

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

MeSH terms

  • Androstadienes / pharmacology
  • Animals
  • Cell Polarity / physiology
  • Chemotaxis / drug effects
  • Chemotaxis / physiology*
  • GTPase-Activating Proteins
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / metabolism
  • HL-60 Cells
  • Humans
  • Interleukin-8 / genetics
  • Interleukin-8 / metabolism*
  • Mice
  • Mice, Knockout
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neutrophils / cytology
  • Neutrophils / metabolism*
  • Phosphatidylinositol 3-Kinases
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-hck / genetics
  • Proto-Oncogene Proteins c-hck / metabolism
  • Pyrimidines / pharmacology
  • RAC2 GTP-Binding Protein
  • Receptors, Interleukin-8B / genetics
  • Receptors, Interleukin-8B / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Wortmannin
  • rac GTP-Binding Proteins / genetics
  • rac GTP-Binding Proteins / metabolism*
  • src-Family Kinases / genetics
  • src-Family Kinases / metabolism*

Substances

  • AG 1879
  • Androstadienes
  • CXCL8 protein, human
  • DOCK2 protein, human
  • DOCK3 protein, human
  • FGD1-related Cdc42-GEF protein, human
  • GTPase-Activating Proteins
  • Guanine Nucleotide Exchange Factors
  • Interleukin-8
  • Nerve Tissue Proteins
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Receptors, Interleukin-8B
  • HCK protein, human
  • Hck protein, mouse
  • Proto-Oncogene Proteins c-hck
  • lyn protein-tyrosine kinase
  • src-Family Kinases
  • rac GTP-Binding Proteins
  • Wortmannin