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Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models
Dimethyl fumarate is an orally bioavailable compound for the treatment of multiple sclerosis and psoriasis. A mechanism involving nuclear factor erythroid 2-like 2 activation has been proposed to account for its efficacy in multiple sclerosis. Here, we report that dimethyl fumarate inhibits expressi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603381/ https://www.ncbi.nlm.nih.gov/pubmed/26478898 http://dx.doi.org/10.1002/acn3.251 |
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author | Kihara, Yasuyuki Groves, Aran Rivera, Richard R Chun, Jerold |
author_facet | Kihara, Yasuyuki Groves, Aran Rivera, Richard R Chun, Jerold |
author_sort | Kihara, Yasuyuki |
collection | PubMed |
description | Dimethyl fumarate is an orally bioavailable compound for the treatment of multiple sclerosis and psoriasis. A mechanism involving nuclear factor erythroid 2-like 2 activation has been proposed to account for its efficacy in multiple sclerosis. Here, we report that dimethyl fumarate inhibits expression of integrin α4 on circulating lymphocytes in experimental autoimmune encephalomyelitis mice and also on activated human Jurkat T cells in a manner distinct from nuclear factor erythroid 2-like 2 activation. Our results offer an alternative mechanism for the efficacy of dimethyl fumarate in multiple sclerosis. |
format | Online Article Text |
id | pubmed-4603381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46033812015-10-16 Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models Kihara, Yasuyuki Groves, Aran Rivera, Richard R Chun, Jerold Ann Clin Transl Neurol Brief Communications Dimethyl fumarate is an orally bioavailable compound for the treatment of multiple sclerosis and psoriasis. A mechanism involving nuclear factor erythroid 2-like 2 activation has been proposed to account for its efficacy in multiple sclerosis. Here, we report that dimethyl fumarate inhibits expression of integrin α4 on circulating lymphocytes in experimental autoimmune encephalomyelitis mice and also on activated human Jurkat T cells in a manner distinct from nuclear factor erythroid 2-like 2 activation. Our results offer an alternative mechanism for the efficacy of dimethyl fumarate in multiple sclerosis. John Wiley & Sons, Ltd 2015-10 2015-09-11 /pmc/articles/PMC4603381/ /pubmed/26478898 http://dx.doi.org/10.1002/acn3.251 Text en © 2015 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Brief Communications Kihara, Yasuyuki Groves, Aran Rivera, Richard R Chun, Jerold Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models |
title | Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models |
title_full | Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models |
title_fullStr | Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models |
title_full_unstemmed | Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models |
title_short | Dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models |
title_sort | dimethyl fumarate inhibits integrin α4 expression in multiple sclerosis models |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603381/ https://www.ncbi.nlm.nih.gov/pubmed/26478898 http://dx.doi.org/10.1002/acn3.251 |
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