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Regulation of Immune Cell Migration by Sphingosine-1-Phosphate

Sphingosine-1-phosphate [S1P] is a potent bioactive sphingolipid molecule. In response to a stimulus, S1P is produced intracellularly by the action of two sphingosine kinases, and then it is exported to the extracellular environment or acts as an intracellular second messenger. S1P binds to its cogn...

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Detalles Bibliográficos
Autores principales: Kumar, A., Saba, JD.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169313/
https://www.ncbi.nlm.nih.gov/pubmed/30294722
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author Kumar, A.
Saba, JD.
author_facet Kumar, A.
Saba, JD.
author_sort Kumar, A.
collection PubMed
description Sphingosine-1-phosphate [S1P] is a potent bioactive sphingolipid molecule. In response to a stimulus, S1P is produced intracellularly by the action of two sphingosine kinases, and then it is exported to the extracellular environment or acts as an intracellular second messenger. S1P binds to its cognate G-protein coupled receptors, which are known as S1P receptors. There are five S1P receptors that have been identified in vertebrates. By activating S1P receptors, S1P controls a variety of physiological and pathological processes including cell migration, angiogenesis, vascular maturation, inflammation, and invasion, metastasis, and chemoresistance in cancer. S1P has emerged as a critical regulator of leukocyte migration and plays a central role in lymphocyte egress from the thymus and secondary lymphoid organs. In the current review article, we summarize the current understanding of the emigration of lymphocytes and other leukocytes from bone marrow, thymus and secondary lymphoid organs to the circulation, as well as the clinical implications of modulating the activity of the major S1P receptor, S1PR1.
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spelling pubmed-61693132018-10-03 Regulation of Immune Cell Migration by Sphingosine-1-Phosphate Kumar, A. Saba, JD. Cell Mol Biol (OMICS) Article Sphingosine-1-phosphate [S1P] is a potent bioactive sphingolipid molecule. In response to a stimulus, S1P is produced intracellularly by the action of two sphingosine kinases, and then it is exported to the extracellular environment or acts as an intracellular second messenger. S1P binds to its cognate G-protein coupled receptors, which are known as S1P receptors. There are five S1P receptors that have been identified in vertebrates. By activating S1P receptors, S1P controls a variety of physiological and pathological processes including cell migration, angiogenesis, vascular maturation, inflammation, and invasion, metastasis, and chemoresistance in cancer. S1P has emerged as a critical regulator of leukocyte migration and plays a central role in lymphocyte egress from the thymus and secondary lymphoid organs. In the current review article, we summarize the current understanding of the emigration of lymphocytes and other leukocytes from bone marrow, thymus and secondary lymphoid organs to the circulation, as well as the clinical implications of modulating the activity of the major S1P receptor, S1PR1. 2015-12-31 2015 /pmc/articles/PMC6169313/ /pubmed/30294722 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Kumar, A.
Saba, JD.
Regulation of Immune Cell Migration by Sphingosine-1-Phosphate
title Regulation of Immune Cell Migration by Sphingosine-1-Phosphate
title_full Regulation of Immune Cell Migration by Sphingosine-1-Phosphate
title_fullStr Regulation of Immune Cell Migration by Sphingosine-1-Phosphate
title_full_unstemmed Regulation of Immune Cell Migration by Sphingosine-1-Phosphate
title_short Regulation of Immune Cell Migration by Sphingosine-1-Phosphate
title_sort regulation of immune cell migration by sphingosine-1-phosphate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169313/
https://www.ncbi.nlm.nih.gov/pubmed/30294722
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