Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: McGowan, Jenna, Peter, Cara, Chattopadhyay, Saurabh, Chakravarti, Ritu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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
_version_ 1783440068827938816
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
work_keys_str_mv AT mcgowanjenna 1433zanovelimmunogenpromotesinflammatorycytokineproduction
AT petercara 1433zanovelimmunogenpromotesinflammatorycytokineproduction
AT chattopadhyaysaurabh 1433zanovelimmunogenpromotesinflammatorycytokineproduction
AT chakravartiritu 1433zanovelimmunogenpromotesinflammatorycytokineproduction