RACK1 regulates directional cell migration by acting on gβγ at the interface with its effectors PLCβ and PI3Kγ

Songhai Chen, Fang Lin, Eun Shin Myung, Fei Wang, Lixin Shen, Heidi E. Hamm

Research output: Contribution to journalArticle

Abstract

Migration of cells up the chemoattractant gradients is mediated by the binding of chemoattractants to G protein-coupled receptors and activation of a network of coordinated excitatory and inhibitory signals. Although the excitatory process has been well studied, the molecular nature of the inhibitory signals remains largely elusive. Here we report that the receptor for activated C kinase 1 (RACK1), a novel binding protein of heterotrimeric G protein βγ (Gβγ) subunits, acts as a negative regulator of directed cell migration. After chemoattractant-induced polarization of Jurkat and neutrophil-like differentiated HL60 (dHL60) cells, RACK1 interacts with Gβγ and is recruited to the leading edge. Down-regulation of RACK1 dramatically enhances chemotaxis of cells, whereas overexpression of RACK1 or a fragment of RACK1 that retains Gβγ-binding capacity inhibits cell migration. Further studies reveal that RACK1 does not modulate cell migration through binding to other known interacting proteins such as PKCβ and Src. Rather, RACK1 selectively inhibits Gβγ-stimulated phosphatidylinositol 3-kinase γ (PI3Kγ) and phospholipase C (PLC) β activity, due to the competitive binding of RACK1, PI3Kγ, and PLCβ to Gβγ. Taken together, these findings provide a novel mechanism of regulating cell migration, i.e., RACK1-mediated interference with Gβγ-dependent activation of key effectors critical for chemotaxis.

Original languageEnglish (US)
Pages (from-to)3909-3922
Number of pages14
JournalMolecular biology of the cell
Volume19
Issue number9
DOIs
StatePublished - Sep 1 2008

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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