| Literature DB >> 17002593 |
Abstract
Beta-arrestins have recently emerged as key regulators of directed cell migration or chemotaxis. Given their traditional role as mediators of receptor desensitization, one theory is that beta-arrestins contribute to cell polarity during chemotaxis by quenching the signal at the trailing edge of the cell. A second theory is that they scaffold signaling molecules involved in cytoskeletal reorganization to promote localized actin assembly events leading to the formation of a leading edge. This review addresses both models. It discusses studies demonstrating the involvement of beta-arrestins in chemotaxis both in vivo and in vitro as well as recent evidence that beta-arrestins directly bind and regulate proteins involved in actin reorganization.Mesh:
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Year: 2007 PMID: 17002593 DOI: 10.1146/annurev.physiol.69.022405.154804
Source DB: PubMed Journal: Annu Rev Physiol ISSN: 0066-4278 Impact factor: 19.318