FASEB J. Avanti Polar Lipids
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published as doi: 10.1096/fj.06-7420com.
(The FASEB Journal. 2007;21:1503-1514.)
© 2007 FASEB
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
fj.06-7420comv1
21/7/1503    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Novgorodov, A. S.
Right arrow Articles by Gudz, T. I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Novgorodov, A. S.
Right arrow Articles by Gudz, T. I.

Activation of sphingosine-1-phosphate receptor S1P5 inhibits oligodendrocyte progenitor migration

Alexander S. Novgorodov{dagger}, Mazen El-Alwani{ddagger}, Jacek Bielawski§, Lina M. Obeid*,{ddagger} and Tatyana I. Gudz*,{dagger},1

* Ralph H. Johnson Veterans Affairs Medical Center, and the Departments of

{dagger} Neuroscience,

{ddagger} Medicine and

§ Biochemistry of Medical University of South Carolina, Charleston, South Carolina, USA

1Correspondence: Department of Neuroscience, Medical University of South Carolina, 114 Doughty St. Charleston, SC 29425, USA. E-mail: gudz{at}musc.edu

Sphingosine-1-phosphate (S1P) acts as an extracellular ligand for a family of G-protein coupled receptors that are crucial in cell migration. S1P5 is exclusively expressed in oligodendrocytes and oligodendrocyte precursor cells (OPCs), which migrate considerable distances during brain development. The current studies suggest a physiological role for S1P and S1P5 in regulation of OPC migration. mRNA expression levels of S1P2 and S1P5 are comparable in OPCs, but S1P binding specifically to the S1P5 receptor blocked OPC migration (IC50=29 nM). Thus, knocking down S1P5 using siRNA prevented the S1P-induced decrease in OPC migration, whereas knocking down S1P2 did not have any effect. S1P-induced modulation of OPC migration was insensitive to pertussis toxin, suggesting that S1P5-initiated signaling is not mediated by the G{alpha}i-protein coupled pathway. Furthermore, S1P5 appears to engage the G{alpha}12/13 protein coupled Rho/ROCK signaling pathway to impede OPC migration. To modulate OPC motility, extracellular S1P could be derived from the export of intracellular S1P generated in response to glutamate treatment of OPCs. These studies suggest that S1P could be a part of the neuron-oligodendroglial communication network regulating OPC migration and may provide directional guidance cues for migrating OPCs in the developing brain.—Novgorodov, A. S., El-Alwani, M., Bielawski, J., Obeid, L. M., Gudz, T. I. Activation of sphingosine-1-phosphate receptor S1P5 inhibits oligodendrocyte progenitor migration.


Key Words: brain development • S1P2 receptor • FTY720 • directional guidance cue




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
D. A. Chudakova, Y. H. Zeidan, B. W. Wheeler, J. Yu, S. A. Novgorodov, M. S. Kindy, Y. A. Hannun, and T. I. Gudz
Integrin-associated Lyn Kinase Promotes Cell Survival by Suppressing Acid Sphingomyelinase Activity
J. Biol. Chem., October 24, 2008; 283(43): 28806 - 28816.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
V. E. Miron, J. A. Hall, T. E. Kennedy, B. Soliven, and J. P. Antel
Cyclical and Dose-Dependent Responses of Adult Human Mature Oligodendrocytes to Fingolimod
Am. J. Pathol., October 1, 2008; 173(4): 1143 - 1152.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by The Federation of American Societies for Experimental Biology.