RACK1 regulates directional cell migration by acting on G betagamma at the interface with its effectors PLC beta and PI3K gamma.

Chen S, Lin F, Shin ME, Wang F, Shen L, Hamm HE
Mol Biol Cell. 2008 19 (9): 3909-22

PMID: 18596232 · PMCID: PMC2526680 · DOI:10.1091/mbc.e08-04-0433

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 betagamma (G betagamma) 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 G betagamma 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 G betagamma-binding capacity inhibits cell migration. Further studies reveal that RACK1 does not modulate cell migration through binding to other known interacting proteins such as PKC beta and Src. Rather, RACK1 selectively inhibits G betagamma-stimulated phosphatidylinositol 3-kinase gamma (PI3K gamma) and phospholipase C (PLC) beta activity, due to the competitive binding of RACK1, PI3K gamma, and PLC beta to G betagamma. Taken together, these findings provide a novel mechanism of regulating cell migration, i.e., RACK1-mediated interference with G betagamma-dependent activation of key effectors critical for chemotaxis.

MeSH Terms (21)

Cell Movement Chemotaxis Class Ib Phosphatidylinositol 3-Kinase Enzyme Inhibitors Gene Expression Regulation GTP-Binding Protein beta Subunits GTP-Binding Protein gamma Subunits GTP-Binding Proteins HL-60 Cells Humans Isoenzymes Jurkat Cells Models, Molecular Models, Theoretical Neoplasm Proteins Neutrophils Phosphatidylinositol 3-Kinases Phospholipase C beta Receptors, Cell Surface Receptors for Activated C Kinase RNA, Small Interfering

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