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The Gas6/TAM System and Multiple Sclerosis
Growth arrest specific 6 (Gas6) is a multimodular circulating protein, the biological actions of which are mediated by the interaction with three transmembrane tyrosine kinase receptors: Tyro3, Axl, and MerTK, collectively named TAM. Over the last few decades, many progresses have been done in the u...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133808/ https://www.ncbi.nlm.nih.gov/pubmed/27801848 http://dx.doi.org/10.3390/ijms17111807 |
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author | Bellan, Mattia Pirisi, Mario Sainaghi, Pier Paolo |
author_facet | Bellan, Mattia Pirisi, Mario Sainaghi, Pier Paolo |
author_sort | Bellan, Mattia |
collection | PubMed |
description | Growth arrest specific 6 (Gas6) is a multimodular circulating protein, the biological actions of which are mediated by the interaction with three transmembrane tyrosine kinase receptors: Tyro3, Axl, and MerTK, collectively named TAM. Over the last few decades, many progresses have been done in the understanding of the biological activities of this highly pleiotropic system, which plays a role in the regulation of immune response, inflammation, coagulation, cell growth, and clearance of apoptotic bodies. Recent findings have further related Gas6 and TAM receptors to neuroinflammation in general and, specifically, to multiple sclerosis (MS). In this paper, we review the biology of the Gas6/TAM system and the current evidence supporting its potential role in the pathogenesis of MS. |
format | Online Article Text |
id | pubmed-5133808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-51338082016-12-12 The Gas6/TAM System and Multiple Sclerosis Bellan, Mattia Pirisi, Mario Sainaghi, Pier Paolo Int J Mol Sci Review Growth arrest specific 6 (Gas6) is a multimodular circulating protein, the biological actions of which are mediated by the interaction with three transmembrane tyrosine kinase receptors: Tyro3, Axl, and MerTK, collectively named TAM. Over the last few decades, many progresses have been done in the understanding of the biological activities of this highly pleiotropic system, which plays a role in the regulation of immune response, inflammation, coagulation, cell growth, and clearance of apoptotic bodies. Recent findings have further related Gas6 and TAM receptors to neuroinflammation in general and, specifically, to multiple sclerosis (MS). In this paper, we review the biology of the Gas6/TAM system and the current evidence supporting its potential role in the pathogenesis of MS. MDPI 2016-10-28 /pmc/articles/PMC5133808/ /pubmed/27801848 http://dx.doi.org/10.3390/ijms17111807 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bellan, Mattia Pirisi, Mario Sainaghi, Pier Paolo The Gas6/TAM System and Multiple Sclerosis |
title | The Gas6/TAM System and Multiple Sclerosis |
title_full | The Gas6/TAM System and Multiple Sclerosis |
title_fullStr | The Gas6/TAM System and Multiple Sclerosis |
title_full_unstemmed | The Gas6/TAM System and Multiple Sclerosis |
title_short | The Gas6/TAM System and Multiple Sclerosis |
title_sort | gas6/tam system and multiple sclerosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133808/ https://www.ncbi.nlm.nih.gov/pubmed/27801848 http://dx.doi.org/10.3390/ijms17111807 |
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