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IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells
IL-36γ is a proinflamatory cytokine which belongs to the IL-1 family of cytokines. It is expressed in the skin and by epithelial cells (ECs) lining lung and gut tissue. We used human 3-D organotypic cells, that recapitulate either in vivo human vaginal or cervical tissue, to explore the possible rol...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911402/ https://www.ncbi.nlm.nih.gov/pubmed/27379082 http://dx.doi.org/10.3389/fmicb.2016.00955 |
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author | Winkle, Sean M. Throop, Andrea L. Herbst-Kralovetz, Melissa M. |
author_facet | Winkle, Sean M. Throop, Andrea L. Herbst-Kralovetz, Melissa M. |
author_sort | Winkle, Sean M. |
collection | PubMed |
description | IL-36γ is a proinflamatory cytokine which belongs to the IL-1 family of cytokines. It is expressed in the skin and by epithelial cells (ECs) lining lung and gut tissue. We used human 3-D organotypic cells, that recapitulate either in vivo human vaginal or cervical tissue, to explore the possible role of IL-36γ in host defense against pathogens in the human female reproductive tract (FRT). EC were exposed to compounds derived from virus or bacterial sources and induction and regulation of IL-36γ and its receptor was determined. Polyinosinic-polycytidylic acid (poly I:C), flagellin, and synthetic lipoprotein (FSL-1) significantly induced expression of IL-36γ in a dose-dependent manner, and appeared to be TLR-dependent. Recombinant IL-36γ treatment resulted in self-amplification of IL-36γ and its receptor (IL-36R) via increased gene expression, and promoted other inflammatory signaling pathways. This is the first report to demonstrate that the IL-36 receptor and IL-36γ are present in the human FRT EC and that they are differentially induced by microbial products at this site. We conclude that IL-36γ is a driver for epithelial and immune activation following microbial insult and, as such, may play a critical role in host defense in the FRT. |
format | Online Article Text |
id | pubmed-4911402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49114022016-07-04 IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells Winkle, Sean M. Throop, Andrea L. Herbst-Kralovetz, Melissa M. Front Microbiol Microbiology IL-36γ is a proinflamatory cytokine which belongs to the IL-1 family of cytokines. It is expressed in the skin and by epithelial cells (ECs) lining lung and gut tissue. We used human 3-D organotypic cells, that recapitulate either in vivo human vaginal or cervical tissue, to explore the possible role of IL-36γ in host defense against pathogens in the human female reproductive tract (FRT). EC were exposed to compounds derived from virus or bacterial sources and induction and regulation of IL-36γ and its receptor was determined. Polyinosinic-polycytidylic acid (poly I:C), flagellin, and synthetic lipoprotein (FSL-1) significantly induced expression of IL-36γ in a dose-dependent manner, and appeared to be TLR-dependent. Recombinant IL-36γ treatment resulted in self-amplification of IL-36γ and its receptor (IL-36R) via increased gene expression, and promoted other inflammatory signaling pathways. This is the first report to demonstrate that the IL-36 receptor and IL-36γ are present in the human FRT EC and that they are differentially induced by microbial products at this site. We conclude that IL-36γ is a driver for epithelial and immune activation following microbial insult and, as such, may play a critical role in host defense in the FRT. Frontiers Media S.A. 2016-06-17 /pmc/articles/PMC4911402/ /pubmed/27379082 http://dx.doi.org/10.3389/fmicb.2016.00955 Text en Copyright © 2016 Winkle, Throop and Herbst-Kralovetz. 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) or licensor 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 | Microbiology Winkle, Sean M. Throop, Andrea L. Herbst-Kralovetz, Melissa M. IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells |
title | IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells |
title_full | IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells |
title_fullStr | IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells |
title_full_unstemmed | IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells |
title_short | IL-36γ Augments Host Defense and Immune Responses in Human Female Reproductive Tract Epithelial Cells |
title_sort | il-36γ augments host defense and immune responses in human female reproductive tract epithelial cells |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911402/ https://www.ncbi.nlm.nih.gov/pubmed/27379082 http://dx.doi.org/10.3389/fmicb.2016.00955 |
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