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First published online February 20, 2008
doi: 10.1242/jcs.023333

Journal of Cell Science 121, 551-559 (2008)
Published by The Company of Biologists 2008
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Commentary

The regulation of cell motility and chemotaxis by phospholipid signaling

Verena Kölsch, Pascale G. Charest and Richard A. Firtel*

Section of Cell and Developmental Biology, Division of Biological Sciences, Center for Molecular Genetics, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0380, USA

* Author for correspondence (e-mail: rafirtel{at}ucsd.edu)

Accepted 22 November 2007

Phosphoinositide 3-kinase (PI3K), PTEN and localized phosphatidylinositol (3,4,5)-trisphosphate [PtdIns(3,4,5)P3] play key roles in chemotaxis, regulating cell motility by controlling the actin cytoskeleton in Dictyostelium and mammalian cells. PtdIns(3,4,5)P3, produced by PI3K, acts via diverse downstream signaling components, including the GTPase Rac, Arf-GTPases and the kinase Akt (PKB). It has become increasingly apparent, however, that chemotaxis results from an interplay between the PI3K-PTEN pathway and other parallel pathways in Dictyostelium and mammalian cells. In Dictyostelium, the phospholipase PLA2 acts in concert with PI3K to regulate chemotaxis, whereas phospholipase C (PLC) plays a supporting role in modulating PI3K activity. In adenocarcinoma cells, PLC and the actin regulator cofilin seem to provide the direction-sensing machinery, whereas PI3K might regulate motility.

Key words: Dictyostelium, Phospholipase, PTEN, Phosphatidylinositol (3,4,5)-trisphosphate [PtdIns(3,4,5)P3], Ras, Cytoskeleton


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