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


     


Published as doi: 10.1096/fj.07-9087com.
(The FASEB Journal. 2008;22:307-315.)
© 2008 FASEB
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
fj.07-9087comv1
22/1/307    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 Allende, M. L.
Right arrow Articles by Proia, R. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Allende, M. L.
Right arrow Articles by Proia, R. L.
(The FASEB Journal. 2008;22:307-315.)
© 2008 FASEB

S1P1 receptor expression regulates emergence of NKT cells in peripheral tissues

Maria L. Allende*,1, Dapeng Zhou{dagger}, Danielle N. Kalkofen*, Sonia Benhamed*, Galina Tuymetova*, Christine Borowski{ddagger}, Albert Bendelac{ddagger} and Richard L. Proia*,1

* Genetics of Development and Disease Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA;

{dagger} Department of Melanoma Medical Oncology, MD Anderson Cancer Center, University of Texas, Houston, Texas, USA; and

{ddagger} Committee on Immunology, University of Chicago and Howard Hughes Medical Institute, Chicago, Illinois, USA

1Correspondence: R.L.P. and M.L.A., National Institute of Diabetes and Digestive and Kidney Diseases, Bldg. 10, Room 9D-06, 10 Center DR MSC 1821, Bethesda, MD 20892-1821, USA. E-mail: R.L.P., proia{at}nih.gov; M.L.A., mariaa{at}intra.niddk.nih.gov

The S1P1 receptor, on the surface of lymphocytes and endothelial cells, regulates the unique trafficking behavior of certain lymphocyte populations. We have examined whether the S1P1 receptor also dictates the distinctive tissue distribution of V{alpha}14-J{alpha}18 natural killer T (NKT) cells, whose trafficking pattern is not well understood. Mice (TCS1P1KO) were established with a conditional deletion of the S1P1 receptor in thymocytes that included precursors of NKT cells. Within the thymus, NKT cells were found at normal or increased levels, indicating that S1P1 receptor expression was dispensable for NKT cell development. However, substantially reduced numbers of NKT cells were detected in the peripheral tissues of the TCS1P1KO mice. Short-term S1P1 deletion after NKT cells had established residence in the periphery did not substantially alter their distribution in tissues, except for a partial decrease in the spleen. FTY720, a S1P1 receptor ligand that has potent effects on the trafficking of conventional T cells, did not alter the preexisting distribution of NKT cells within peripheral tissues of wild-type mice. Our results indicate that the S1P1 receptor expression on NKT cells is dispensable for development within thymus but is essential for the establishment of their tissue residency in the periphery.—Allende, M. L., Zhou, D., Kalkofen, D. N., Benhamed, S., Tuymetova, G., Borowski, C., Bendelac, A., Proia, R. L. S1P1 receptor expression regulates emergence of NKT cells in peripheral tissues.


Key Words: lipid signaling • G-protein coupled receptors • lymphocyte trafficking • conditional knockout mice




This article has been cited by other articles:


Home page
J. Immunol.Home page
A. Astrakhan, H. D. Ochs, and D. J. Rawlings
Wiskott-Aldrich Syndrome Protein Is Required for Homeostasis and Function of Invariant NKT Cells
J. Immunol., June 15, 2009; 182(12): 7370 - 7380.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by The Federation of American Societies for Experimental Biology.