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14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production
The presence of autoantibodies against 14-3-3ζ in human autoimmune diseases indicates its antigenic function. However, neither the cause nor the consequence of this newly-identified antigenic function of 14-3-3ζ protein is known. To address this, we investigated the immunological functions of 14-3-3...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667649/ https://www.ncbi.nlm.nih.gov/pubmed/31396202 http://dx.doi.org/10.3389/fimmu.2019.01553 |
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author | McGowan, Jenna Peter, Cara Chattopadhyay, Saurabh Chakravarti, Ritu |
author_facet | McGowan, Jenna Peter, Cara Chattopadhyay, Saurabh Chakravarti, Ritu |
author_sort | McGowan, Jenna |
collection | PubMed |
description | The presence of autoantibodies against 14-3-3ζ in human autoimmune diseases indicates its antigenic function. However, neither the cause nor the consequence of this newly-identified antigenic function of 14-3-3ζ protein is known. To address this, we investigated the immunological functions of 14-3-3ζ by studying ex vivo effects on human peripheral blood mononuclear cells (PBMC) proliferation, polarization, and cytokine production. Exogenous 14-3-3ζ promoted PBMC proliferation and T cell polarization toward Th1 and Th17 populations. Significant increases in IFN-γ and IL-17 levels were observed in the presence of 14-3-3ζ. A specific increase in Th1 cells and IFN-γ production provided strong evidence for MHC class II presentation of 14-3-3ζ antigen. Particularly HLA-DRB1(*)0401 allele strongly promoted 14-3-3ζ-induced IFN-γ producing cells. In contrast, prednisolone treatment suppressed both 14-3-3ζ-induced T cell polarization and cytokine production. Overall, we show that MHC presentation and the adaptor functions of 14-3-3ζ participate in promoting IFN-γ and IL-17 production, two of the cytokines commonly associated with autoimmune diseases. To the best of our knowledge, this is the first report describing the ex vivo antigenic function of 14-3-3ζ with human PBMC, thereby providing the basis of its immunological role in human diseases. |
format | Online Article Text |
id | pubmed-6667649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66676492019-08-08 14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production McGowan, Jenna Peter, Cara Chattopadhyay, Saurabh Chakravarti, Ritu Front Immunol Immunology The presence of autoantibodies against 14-3-3ζ in human autoimmune diseases indicates its antigenic function. However, neither the cause nor the consequence of this newly-identified antigenic function of 14-3-3ζ protein is known. To address this, we investigated the immunological functions of 14-3-3ζ by studying ex vivo effects on human peripheral blood mononuclear cells (PBMC) proliferation, polarization, and cytokine production. Exogenous 14-3-3ζ promoted PBMC proliferation and T cell polarization toward Th1 and Th17 populations. Significant increases in IFN-γ and IL-17 levels were observed in the presence of 14-3-3ζ. A specific increase in Th1 cells and IFN-γ production provided strong evidence for MHC class II presentation of 14-3-3ζ antigen. Particularly HLA-DRB1(*)0401 allele strongly promoted 14-3-3ζ-induced IFN-γ producing cells. In contrast, prednisolone treatment suppressed both 14-3-3ζ-induced T cell polarization and cytokine production. Overall, we show that MHC presentation and the adaptor functions of 14-3-3ζ participate in promoting IFN-γ and IL-17 production, two of the cytokines commonly associated with autoimmune diseases. To the best of our knowledge, this is the first report describing the ex vivo antigenic function of 14-3-3ζ with human PBMC, thereby providing the basis of its immunological role in human diseases. Frontiers Media S.A. 2019-07-24 /pmc/articles/PMC6667649/ /pubmed/31396202 http://dx.doi.org/10.3389/fimmu.2019.01553 Text en Copyright © 2019 McGowan, Peter, Chattopadhyay and Chakravarti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology McGowan, Jenna Peter, Cara Chattopadhyay, Saurabh Chakravarti, Ritu 14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production |
title | 14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production |
title_full | 14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production |
title_fullStr | 14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production |
title_full_unstemmed | 14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production |
title_short | 14-3-3ζ-A Novel Immunogen Promotes Inflammatory Cytokine Production |
title_sort | 14-3-3ζ-a novel immunogen promotes inflammatory cytokine production |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667649/ https://www.ncbi.nlm.nih.gov/pubmed/31396202 http://dx.doi.org/10.3389/fimmu.2019.01553 |
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