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TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity

The TGFβ superfamily is composed of more than 33 growth and differentiation factors, including TGFβ1, β2, β3, BMPs, GDFs, nodal-related proteins, and activins. These members usually exert pleiotropic actions on several tissues and control multiple cellular processes, such as cell growth, cell surviv...

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Detalles Bibliográficos
Autores principales: Tamayo, Esther, Alvarez, Pilar, Merino, Ramón
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321615/
https://www.ncbi.nlm.nih.gov/pubmed/30544541
http://dx.doi.org/10.3390/ijms19123928
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author Tamayo, Esther
Alvarez, Pilar
Merino, Ramón
author_facet Tamayo, Esther
Alvarez, Pilar
Merino, Ramón
author_sort Tamayo, Esther
collection PubMed
description The TGFβ superfamily is composed of more than 33 growth and differentiation factors, including TGFβ1, β2, β3, BMPs, GDFs, nodal-related proteins, and activins. These members usually exert pleiotropic actions on several tissues and control multiple cellular processes, such as cell growth, cell survival, cell migration, cell fate specification, and differentiation, both during embryonic development and postnatal life. Although the effects of these factors on immune responses were elucidated long ago, most studies have been focused on the actions of TGFβs on T cells, as major regulators of adaptive immunity. In this review, we discuss new findings about the involvement of TGFβ superfamily members in the control of B cell development and function. Moreover, the potential contribution of TGFβ signaling to control B cell-mediated autoimmune diseases and its utility in the design of new therapies are also discussed.
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spelling pubmed-63216152019-01-07 TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity Tamayo, Esther Alvarez, Pilar Merino, Ramón Int J Mol Sci Review The TGFβ superfamily is composed of more than 33 growth and differentiation factors, including TGFβ1, β2, β3, BMPs, GDFs, nodal-related proteins, and activins. These members usually exert pleiotropic actions on several tissues and control multiple cellular processes, such as cell growth, cell survival, cell migration, cell fate specification, and differentiation, both during embryonic development and postnatal life. Although the effects of these factors on immune responses were elucidated long ago, most studies have been focused on the actions of TGFβs on T cells, as major regulators of adaptive immunity. In this review, we discuss new findings about the involvement of TGFβ superfamily members in the control of B cell development and function. Moreover, the potential contribution of TGFβ signaling to control B cell-mediated autoimmune diseases and its utility in the design of new therapies are also discussed. MDPI 2018-12-07 /pmc/articles/PMC6321615/ /pubmed/30544541 http://dx.doi.org/10.3390/ijms19123928 Text en © 2018 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
Tamayo, Esther
Alvarez, Pilar
Merino, Ramón
TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity
title TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity
title_full TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity
title_fullStr TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity
title_full_unstemmed TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity
title_short TGFβ Superfamily Members as Regulators of B Cell Development and Function—Implications for Autoimmunity
title_sort tgfβ superfamily members as regulators of b cell development and function—implications for autoimmunity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321615/
https://www.ncbi.nlm.nih.gov/pubmed/30544541
http://dx.doi.org/10.3390/ijms19123928
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