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Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites

Inflammation can be protective or pathogenic depending on context and timeframe. Acute inflammation, including the accumulation of CD4 T cells, accompanies protective immune responses to pathogens, but the presence of activated CD4 T cells at sites of inflammation is associated with chronic inflamma...

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Autores principales: Jaigirdar, Shafqat Ahrar, Benson, Robert A., Elmesmari, Aziza, Kurowska-Stolarska, Mariola Stefania, McInnes, Iain B., Garside, Paul, MacLeod, Megan K. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705559/
https://www.ncbi.nlm.nih.gov/pubmed/29225602
http://dx.doi.org/10.3389/fimmu.2017.01627
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author Jaigirdar, Shafqat Ahrar
Benson, Robert A.
Elmesmari, Aziza
Kurowska-Stolarska, Mariola Stefania
McInnes, Iain B.
Garside, Paul
MacLeod, Megan K. L.
author_facet Jaigirdar, Shafqat Ahrar
Benson, Robert A.
Elmesmari, Aziza
Kurowska-Stolarska, Mariola Stefania
McInnes, Iain B.
Garside, Paul
MacLeod, Megan K. L.
author_sort Jaigirdar, Shafqat Ahrar
collection PubMed
description Inflammation can be protective or pathogenic depending on context and timeframe. Acute inflammation, including the accumulation of CD4 T cells, accompanies protective immune responses to pathogens, but the presence of activated CD4 T cells at sites of inflammation is associated with chronic inflammatory disease. While significant progress has been made in understanding the migration of CD4 T cells into inflamed sites, the signals that lead to their persistence are poorly characterized. Using a murine ear model of acute inflammation and intravital two-photon imaging, we have dissected the signals that mediate CD4 T cell persistence. We report the unexpected finding that the bioactive lipid, sphingosine-1-phosphate (S1P), is both necessary and sufficient for the persistence of activated CD4 T cells at peripheral tissues in acute inflammation. S1P mediated the enhanced motility of CD4 T cells at inflamed tissues but did not affect their migration to the downstream draining lymph node. We found that sphingosine kinase-1, which regulates S1P production is increased at inflamed sites in mice and in patients with the chronic inflammatory disease, rheumatoid arthritis. Together, these data suggest that S1P, or its regulators, may be key targets to promote or disrupt accumulation of CD4 T cells at inflamed tissues.
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spelling pubmed-57055592017-12-08 Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites Jaigirdar, Shafqat Ahrar Benson, Robert A. Elmesmari, Aziza Kurowska-Stolarska, Mariola Stefania McInnes, Iain B. Garside, Paul MacLeod, Megan K. L. Front Immunol Immunology Inflammation can be protective or pathogenic depending on context and timeframe. Acute inflammation, including the accumulation of CD4 T cells, accompanies protective immune responses to pathogens, but the presence of activated CD4 T cells at sites of inflammation is associated with chronic inflammatory disease. While significant progress has been made in understanding the migration of CD4 T cells into inflamed sites, the signals that lead to their persistence are poorly characterized. Using a murine ear model of acute inflammation and intravital two-photon imaging, we have dissected the signals that mediate CD4 T cell persistence. We report the unexpected finding that the bioactive lipid, sphingosine-1-phosphate (S1P), is both necessary and sufficient for the persistence of activated CD4 T cells at peripheral tissues in acute inflammation. S1P mediated the enhanced motility of CD4 T cells at inflamed tissues but did not affect their migration to the downstream draining lymph node. We found that sphingosine kinase-1, which regulates S1P production is increased at inflamed sites in mice and in patients with the chronic inflammatory disease, rheumatoid arthritis. Together, these data suggest that S1P, or its regulators, may be key targets to promote or disrupt accumulation of CD4 T cells at inflamed tissues. Frontiers Media S.A. 2017-11-24 /pmc/articles/PMC5705559/ /pubmed/29225602 http://dx.doi.org/10.3389/fimmu.2017.01627 Text en Copyright © 2017 Jaigirdar, Benson, Elmesmari, Kurowska-Stolarska, McInnes, Garside and MacLeod. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Jaigirdar, Shafqat Ahrar
Benson, Robert A.
Elmesmari, Aziza
Kurowska-Stolarska, Mariola Stefania
McInnes, Iain B.
Garside, Paul
MacLeod, Megan K. L.
Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites
title Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites
title_full Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites
title_fullStr Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites
title_full_unstemmed Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites
title_short Sphingosine-1-Phosphate Promotes the Persistence of Activated CD4 T Cells in Inflamed Sites
title_sort sphingosine-1-phosphate promotes the persistence of activated cd4 t cells in inflamed sites
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705559/
https://www.ncbi.nlm.nih.gov/pubmed/29225602
http://dx.doi.org/10.3389/fimmu.2017.01627
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