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Sphingosine Kinases promote IL-17 expression in human T lymphocytes
Sphingosine 1-phosphate (S1P) has a role in many cellular processes. S1P is involved in cell growth and apoptosis, regulation of cell trafficking, production of cytokines and chemokines. The kinases SphK1 and SphK2 (SphKs) phosphorilate Sphingosine (Sph) to S1P and several phosphatases revert S1P to...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125344/ https://www.ncbi.nlm.nih.gov/pubmed/30185808 http://dx.doi.org/10.1038/s41598-018-31666-1 |
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author | Barra, Giusi Lepore, Alessio Gagliardi, Miriam Somma, Domenico Matarazzo, Maria Rosaria Costabile, Francesca Pasquale, Giuseppe Mazzoni, Alessio Gallo, Carmela Nuzzo, Genoveffa Annunziato, Francesco Fontana, Angelo Leonardi, Antonio De Palma, Raffaele |
author_facet | Barra, Giusi Lepore, Alessio Gagliardi, Miriam Somma, Domenico Matarazzo, Maria Rosaria Costabile, Francesca Pasquale, Giuseppe Mazzoni, Alessio Gallo, Carmela Nuzzo, Genoveffa Annunziato, Francesco Fontana, Angelo Leonardi, Antonio De Palma, Raffaele |
author_sort | Barra, Giusi |
collection | PubMed |
description | Sphingosine 1-phosphate (S1P) has a role in many cellular processes. S1P is involved in cell growth and apoptosis, regulation of cell trafficking, production of cytokines and chemokines. The kinases SphK1 and SphK2 (SphKs) phosphorilate Sphingosine (Sph) to S1P and several phosphatases revert S1P to sphingosine, thus assuring a balanced pool that can be depleted by a Sphingosine lyase in hexadecenal compounds and aldehydes. There are evidences that SphK1 and 2 may per se control cellular processes. Here, we report that Sph kinases regulate IL-17 expression in human T cells. SphKs inhibition impairs the production of IL-17, while their overexpression up-regulates expression of the cytokine through acetylation of IL-17 promoter. SphKs were up-regulated also in PBMCs of patients affected by IL-17 related diseases. Thus, S1P/S1P kinases axis is a mechanism likely to promote IL-17 expression in human T cells, representing a possible therapeutic target in human inflammatory diseases. |
format | Online Article Text |
id | pubmed-6125344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61253442018-09-10 Sphingosine Kinases promote IL-17 expression in human T lymphocytes Barra, Giusi Lepore, Alessio Gagliardi, Miriam Somma, Domenico Matarazzo, Maria Rosaria Costabile, Francesca Pasquale, Giuseppe Mazzoni, Alessio Gallo, Carmela Nuzzo, Genoveffa Annunziato, Francesco Fontana, Angelo Leonardi, Antonio De Palma, Raffaele Sci Rep Article Sphingosine 1-phosphate (S1P) has a role in many cellular processes. S1P is involved in cell growth and apoptosis, regulation of cell trafficking, production of cytokines and chemokines. The kinases SphK1 and SphK2 (SphKs) phosphorilate Sphingosine (Sph) to S1P and several phosphatases revert S1P to sphingosine, thus assuring a balanced pool that can be depleted by a Sphingosine lyase in hexadecenal compounds and aldehydes. There are evidences that SphK1 and 2 may per se control cellular processes. Here, we report that Sph kinases regulate IL-17 expression in human T cells. SphKs inhibition impairs the production of IL-17, while their overexpression up-regulates expression of the cytokine through acetylation of IL-17 promoter. SphKs were up-regulated also in PBMCs of patients affected by IL-17 related diseases. Thus, S1P/S1P kinases axis is a mechanism likely to promote IL-17 expression in human T cells, representing a possible therapeutic target in human inflammatory diseases. Nature Publishing Group UK 2018-09-05 /pmc/articles/PMC6125344/ /pubmed/30185808 http://dx.doi.org/10.1038/s41598-018-31666-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Barra, Giusi Lepore, Alessio Gagliardi, Miriam Somma, Domenico Matarazzo, Maria Rosaria Costabile, Francesca Pasquale, Giuseppe Mazzoni, Alessio Gallo, Carmela Nuzzo, Genoveffa Annunziato, Francesco Fontana, Angelo Leonardi, Antonio De Palma, Raffaele Sphingosine Kinases promote IL-17 expression in human T lymphocytes |
title | Sphingosine Kinases promote IL-17 expression in human T lymphocytes |
title_full | Sphingosine Kinases promote IL-17 expression in human T lymphocytes |
title_fullStr | Sphingosine Kinases promote IL-17 expression in human T lymphocytes |
title_full_unstemmed | Sphingosine Kinases promote IL-17 expression in human T lymphocytes |
title_short | Sphingosine Kinases promote IL-17 expression in human T lymphocytes |
title_sort | sphingosine kinases promote il-17 expression in human t lymphocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125344/ https://www.ncbi.nlm.nih.gov/pubmed/30185808 http://dx.doi.org/10.1038/s41598-018-31666-1 |
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