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Promotion of Lymphocyte Egress into Blood and Lymph by Distinct Sources of Sphingosine-1-Phosphate
Lymphocytes require sphingosine-1-phosphate (S1P) receptor-1 to exit lymphoid organs, but the source(s) of extracellular S1P and whether S1P directly promotes egress are unknown. By using mice in which the two kinases that generate S1P were conditionally ablated, we find that plasma S1P is mainly he...
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Published in: | Science (American Association for the Advancement of Science) 2007-04, Vol.316 (5822), p.295-298 |
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creator | Pappu, Rajita Schwab, Susan R Cornelissen, Ivo Pereira, João P Regard, Jean B Xu, Ying Camerer, Eric Zheng, Yao-Wu Huang, Yong Cyster, Jason G Coughlin, Shaun R |
description | Lymphocytes require sphingosine-1-phosphate (S1P) receptor-1 to exit lymphoid organs, but the source(s) of extracellular S1P and whether S1P directly promotes egress are unknown. By using mice in which the two kinases that generate S1P were conditionally ablated, we find that plasma S1P is mainly hematopoietic in origin, with erythrocytes a major contributor, whereas lymph S1P is from a distinct radiation-resistant source. Lymphocyte egress from thymus and secondary lymphoid organs was markedly reduced in kinase-deficient mice. Restoration of S1P to plasma rescued egress to blood but not lymph, and the rescue required lymphocyte expression of S1P-receptor-1. Thus, separate sources provide S1P to plasma and lymph to help lymphocytes exit the low-S1P environment of lymphoid organs. Disruption of compartmentalized S1P signaling is a plausible mechanism by which S1P-receptor-1 agonists function as immunosuppressives. |
doi_str_mv | 10.1126/science.1139221 |
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By using mice in which the two kinases that generate S1P were conditionally ablated, we find that plasma S1P is mainly hematopoietic in origin, with erythrocytes a major contributor, whereas lymph S1P is from a distinct radiation-resistant source. Lymphocyte egress from thymus and secondary lymphoid organs was markedly reduced in kinase-deficient mice. Restoration of S1P to plasma rescued egress to blood but not lymph, and the rescue required lymphocyte expression of S1P-receptor-1. Thus, separate sources provide S1P to plasma and lymph to help lymphocytes exit the low-S1P environment of lymphoid organs. Disruption of compartmentalized S1P signaling is a plausible mechanism by which S1P-receptor-1 agonists function as immunosuppressives.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.1139221</identifier><identifier>PMID: 17363629</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>Washington, DC: American Association for the Advancement of Science</publisher><subject>Animals ; B lymphocytes ; Biological and medical sciences ; Blood ; Blood plasma ; Blood transfusion ; Bone Marrow - metabolism ; Chemotaxis, Leukocyte - physiology ; Chromatography, Liquid ; Endothelium, Vascular ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Genetics of the immune response ; Hematopoietic Stem Cells - metabolism ; Immune system ; Immunobiology ; Kinases ; Lymph ; Lymph nodes ; Lymphocytes ; Lymphocytes - metabolism ; Lymphocytes - physiology ; Lysophospholipids - biosynthesis ; Lysophospholipids - blood ; Lysophospholipids - deficiency ; Lysophospholipids - physiology ; Male ; Mice ; Mice, Inbred C57BL ; Phosphates ; Phosphotransferases (Alcohol Group Acceptor) - genetics ; Phosphotransferases (Alcohol Group Acceptor) - metabolism ; Receptors, Lysosphingolipid - physiology ; Rodents ; Signal transduction ; Sphingosine - analogs & derivatives ; Sphingosine - biosynthesis ; Sphingosine - blood ; Sphingosine - deficiency ; Sphingosine - physiology ; Spleen ; T lymphocytes ; Tandem Mass Spectrometry ; Thymocytes</subject><ispartof>Science (American Association for the Advancement of Science), 2007-04, Vol.316 (5822), p.295-298</ispartof><rights>Copyright 2006 American Association for the Advancement of Science</rights><rights>2008 INIST-CNRS</rights><rights>Copyright American Association for the Advancement of Science Apr 13, 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-7da6a9017ad40319cf2919b2b21bad92595122bf4095f7a3f4ed487dfcff84c33</citedby><cites>FETCH-LOGICAL-c521t-7da6a9017ad40319cf2919b2b21bad92595122bf4095f7a3f4ed487dfcff84c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2882,2883,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18694781$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17363629$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pappu, Rajita</creatorcontrib><creatorcontrib>Schwab, Susan R</creatorcontrib><creatorcontrib>Cornelissen, Ivo</creatorcontrib><creatorcontrib>Pereira, João P</creatorcontrib><creatorcontrib>Regard, Jean B</creatorcontrib><creatorcontrib>Xu, Ying</creatorcontrib><creatorcontrib>Camerer, Eric</creatorcontrib><creatorcontrib>Zheng, Yao-Wu</creatorcontrib><creatorcontrib>Huang, Yong</creatorcontrib><creatorcontrib>Cyster, Jason G</creatorcontrib><creatorcontrib>Coughlin, Shaun R</creatorcontrib><title>Promotion of Lymphocyte Egress into Blood and Lymph by Distinct Sources of Sphingosine-1-Phosphate</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>Lymphocytes require sphingosine-1-phosphate (S1P) receptor-1 to exit lymphoid organs, but the source(s) of extracellular S1P and whether S1P directly promotes egress are unknown. By using mice in which the two kinases that generate S1P were conditionally ablated, we find that plasma S1P is mainly hematopoietic in origin, with erythrocytes a major contributor, whereas lymph S1P is from a distinct radiation-resistant source. Lymphocyte egress from thymus and secondary lymphoid organs was markedly reduced in kinase-deficient mice. Restoration of S1P to plasma rescued egress to blood but not lymph, and the rescue required lymphocyte expression of S1P-receptor-1. Thus, separate sources provide S1P to plasma and lymph to help lymphocytes exit the low-S1P environment of lymphoid organs. Disruption of compartmentalized S1P signaling is a plausible mechanism by which S1P-receptor-1 agonists function as immunosuppressives.</description><subject>Animals</subject><subject>B lymphocytes</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Blood plasma</subject><subject>Blood transfusion</subject><subject>Bone Marrow - metabolism</subject><subject>Chemotaxis, Leukocyte - physiology</subject><subject>Chromatography, Liquid</subject><subject>Endothelium, Vascular</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. 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Academic</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pappu, Rajita</au><au>Schwab, Susan R</au><au>Cornelissen, Ivo</au><au>Pereira, João P</au><au>Regard, Jean B</au><au>Xu, Ying</au><au>Camerer, Eric</au><au>Zheng, Yao-Wu</au><au>Huang, Yong</au><au>Cyster, Jason G</au><au>Coughlin, Shaun R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Promotion of Lymphocyte Egress into Blood and Lymph by Distinct Sources of Sphingosine-1-Phosphate</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>2007-04-13</date><risdate>2007</risdate><volume>316</volume><issue>5822</issue><spage>295</spage><epage>298</epage><pages>295-298</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>Lymphocytes require sphingosine-1-phosphate (S1P) receptor-1 to exit lymphoid organs, but the source(s) of extracellular S1P and whether S1P directly promotes egress are unknown. By using mice in which the two kinases that generate S1P were conditionally ablated, we find that plasma S1P is mainly hematopoietic in origin, with erythrocytes a major contributor, whereas lymph S1P is from a distinct radiation-resistant source. Lymphocyte egress from thymus and secondary lymphoid organs was markedly reduced in kinase-deficient mice. Restoration of S1P to plasma rescued egress to blood but not lymph, and the rescue required lymphocyte expression of S1P-receptor-1. Thus, separate sources provide S1P to plasma and lymph to help lymphocytes exit the low-S1P environment of lymphoid organs. Disruption of compartmentalized S1P signaling is a plausible mechanism by which S1P-receptor-1 agonists function as immunosuppressives.</abstract><cop>Washington, DC</cop><pub>American Association for the Advancement of Science</pub><pmid>17363629</pmid><doi>10.1126/science.1139221</doi><tpages>4</tpages></addata></record> |
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subjects | Animals B lymphocytes Biological and medical sciences Blood Blood plasma Blood transfusion Bone Marrow - metabolism Chemotaxis, Leukocyte - physiology Chromatography, Liquid Endothelium, Vascular Female Fundamental and applied biological sciences. Psychology Fundamental immunology Genetics of the immune response Hematopoietic Stem Cells - metabolism Immune system Immunobiology Kinases Lymph Lymph nodes Lymphocytes Lymphocytes - metabolism Lymphocytes - physiology Lysophospholipids - biosynthesis Lysophospholipids - blood Lysophospholipids - deficiency Lysophospholipids - physiology Male Mice Mice, Inbred C57BL Phosphates Phosphotransferases (Alcohol Group Acceptor) - genetics Phosphotransferases (Alcohol Group Acceptor) - metabolism Receptors, Lysosphingolipid - physiology Rodents Signal transduction Sphingosine - analogs & derivatives Sphingosine - biosynthesis Sphingosine - blood Sphingosine - deficiency Sphingosine - physiology Spleen T lymphocytes Tandem Mass Spectrometry Thymocytes |
title | Promotion of Lymphocyte Egress into Blood and Lymph by Distinct Sources of Sphingosine-1-Phosphate |
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