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Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes

We have recently shown that activin A, a member of TGF-β superfamily, stimulates mouse B cells to express IgA isotype but other isotypes. In the present study, we further characterized effects of activin A on B cell growth and IgA expression. We found that activin A did not have effect on LPS-stimul...

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Detalles Bibliográficos
Autores principales: Lee, Hwa-Joung, Kim, Pyeung-Hyeun
Formato: Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816946/
https://www.ncbi.nlm.nih.gov/pubmed/20157600
http://dx.doi.org/10.4110/in.2009.9.4.133
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author Lee, Hwa-Joung
Kim, Pyeung-Hyeun
author_facet Lee, Hwa-Joung
Kim, Pyeung-Hyeun
author_sort Lee, Hwa-Joung
collection PubMed
description We have recently shown that activin A, a member of TGF-β superfamily, stimulates mouse B cells to express IgA isotype but other isotypes. In the present study, we further characterized effects of activin A on B cell growth and IgA expression. We found that activin A did not have effect on LPS-stimulated cell viability. In parallel, CFSE staining analysis revealed that activin A did not alter cell division. An increase of IgA secretion by activin A was completely abrogated by anti-activin A Ab but not by anti-TGFβ1 Ab. In the same conditions, no other isotypes are significantly affected by each antibody treatment. Finally, activin A, as similar to TGF-β1, increased IgA secretion by mesenteric lymph node cells. These results suggest that activin A can specifically stimulate IgA response, independent of TGF-β in the gut.
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spelling pubmed-28169462010-02-12 Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes Lee, Hwa-Joung Kim, Pyeung-Hyeun Immune Netw Original Article We have recently shown that activin A, a member of TGF-β superfamily, stimulates mouse B cells to express IgA isotype but other isotypes. In the present study, we further characterized effects of activin A on B cell growth and IgA expression. We found that activin A did not have effect on LPS-stimulated cell viability. In parallel, CFSE staining analysis revealed that activin A did not alter cell division. An increase of IgA secretion by activin A was completely abrogated by anti-activin A Ab but not by anti-TGFβ1 Ab. In the same conditions, no other isotypes are significantly affected by each antibody treatment. Finally, activin A, as similar to TGF-β1, increased IgA secretion by mesenteric lymph node cells. These results suggest that activin A can specifically stimulate IgA response, independent of TGF-β in the gut. The Korean Association of Immunologists 2009-08 2009-08-31 /pmc/articles/PMC2816946/ /pubmed/20157600 http://dx.doi.org/10.4110/in.2009.9.4.133 Text en Copyright © 2009 The Korean Association of Immunologists http://creativecommons.org/licenses/by-nc/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Hwa-Joung
Kim, Pyeung-Hyeun
Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes
title Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes
title_full Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes
title_fullStr Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes
title_full_unstemmed Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes
title_short Further Characterization of Activin A-induced IgA Response in Murine B Lymphocytes
title_sort further characterization of activin a-induced iga response in murine b lymphocytes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816946/
https://www.ncbi.nlm.nih.gov/pubmed/20157600
http://dx.doi.org/10.4110/in.2009.9.4.133
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