Journal
CELLULAR SIGNALLING
Volume 21, Issue 7, Pages 1207-1217Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2009.03.011
Keywords
Lysophosphatidic acid (LPA) receptor; Ral GTPase; G protein-coupled receptor kinase (GRK); Desensitization; Endocytosis; Phospholipase C (PLC)
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Funding
- Natural Sciences and Engineering Research Council of Canada (NSERC)
- Heart and Stroke Foundation of Ontario
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Lysophosphatidic acid (LPA) is a major constituent of blood and is involved in a variety of physiological and pathophysiological processes. LPA signals via the ubiquitously expressed G protein-coupled receptors (GPCRs), LPA(1) and LPA(2) that are specific for LPA. However, in large, the molecular mechanisms that regulate the signalling of these receptors are unknown. We show that the small GTPase RalA associates with both LPA(1) and LPA(2) in human embryonic kidney (HEK 293) cells and that stimulation of LPA(1) receptors with LPA triggers the activation of RalA. While RalA was not found to play a role in the endocytosis of LPA receptors, we reveal that LPA, receptor stimulation promoted Ral-dependent phospholipase C activity. Furthermore, we found that GRK2 is required for the desensitization of LPA(1) and LPA(2) and have identified a novel interaction between RalA and GRK2, which is promoted by LPA(1) receptor activity. Taken together, these results establish RalA and GRK2 as key regulators of LPA receptor signalling and demonstrate for the first time that LPA(1) activity facilitates the formation of a novel protein complex between these two proteins. (C) 2009 Elsevier Inc. All rights reserved.
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