Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent Manner

The IL-17-producing CD4+ T helper cell (Th17) differentiation is affected by stimulation of the aryl hydrocarbon receptor (AhR) pathway and by hypoxia-inducible factor 1 alpha (HIF-1α). In some cases, Th17 become non-pathogenic and produce IL-10. However, the initiating events triggering this phenot...

Full description

Bibliographic Details
Main Authors: Roman Volchenkov, Vegard Nygaard, Zeynep Sener, Bjørn Steen Skålhegg
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-06-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2017.00698/full
id doaj-2c39a16808ff42b3935219a95503e135
record_format Article
spelling doaj-2c39a16808ff42b3935219a95503e1352020-11-25T01:08:49ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-06-01810.3389/fimmu.2017.00698259536Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent MannerRoman Volchenkov0Vegard Nygaard1Zeynep Sener2Bjørn Steen Skålhegg3Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayDepartment of Core Facilities, Institute for Cancer Research, Oslo University Hospital HF – Radiumhospitalet, Montebello, Oslo, NorwayDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayThe IL-17-producing CD4+ T helper cell (Th17) differentiation is affected by stimulation of the aryl hydrocarbon receptor (AhR) pathway and by hypoxia-inducible factor 1 alpha (HIF-1α). In some cases, Th17 become non-pathogenic and produce IL-10. However, the initiating events triggering this phenotype are yet to be fully understood. Here, we show that such cells may be differentiated at low oxygen and regardless of AhR ligand treatment such as cigarette smoke extract. Hypoxia led to marked alterations of the transcriptome of IL-10-producing Th17 cells affecting genes involved in metabolic, anti-apoptotic, cell cycle, and T cell functional pathways. Moreover, we show that oxygen regulates the expression of CD52, which is a cell surface protein that has been shown to suppress the activation of other T cells upon release. Taken together, these findings suggest a novel ability for Th17 cells to regulate immune responses in vivo in an oxygen-dependent fashion.http://journal.frontiersin.org/article/10.3389/fimmu.2017.00698/fullTh17 cellsIL-17oxygencigarette smokearyl hydrocarbon receptor
collection DOAJ
language English
format Article
sources DOAJ
author Roman Volchenkov
Vegard Nygaard
Zeynep Sener
Bjørn Steen Skålhegg
spellingShingle Roman Volchenkov
Vegard Nygaard
Zeynep Sener
Bjørn Steen Skålhegg
Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent Manner
Frontiers in Immunology
Th17 cells
IL-17
oxygen
cigarette smoke
aryl hydrocarbon receptor
author_facet Roman Volchenkov
Vegard Nygaard
Zeynep Sener
Bjørn Steen Skålhegg
author_sort Roman Volchenkov
title Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent Manner
title_short Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent Manner
title_full Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent Manner
title_fullStr Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent Manner
title_full_unstemmed Th17 Polarization under Hypoxia Results in Increased IL-10 Production in a Pathogen-Independent Manner
title_sort th17 polarization under hypoxia results in increased il-10 production in a pathogen-independent manner
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2017-06-01
description The IL-17-producing CD4+ T helper cell (Th17) differentiation is affected by stimulation of the aryl hydrocarbon receptor (AhR) pathway and by hypoxia-inducible factor 1 alpha (HIF-1α). In some cases, Th17 become non-pathogenic and produce IL-10. However, the initiating events triggering this phenotype are yet to be fully understood. Here, we show that such cells may be differentiated at low oxygen and regardless of AhR ligand treatment such as cigarette smoke extract. Hypoxia led to marked alterations of the transcriptome of IL-10-producing Th17 cells affecting genes involved in metabolic, anti-apoptotic, cell cycle, and T cell functional pathways. Moreover, we show that oxygen regulates the expression of CD52, which is a cell surface protein that has been shown to suppress the activation of other T cells upon release. Taken together, these findings suggest a novel ability for Th17 cells to regulate immune responses in vivo in an oxygen-dependent fashion.
topic Th17 cells
IL-17
oxygen
cigarette smoke
aryl hydrocarbon receptor
url http://journal.frontiersin.org/article/10.3389/fimmu.2017.00698/full
work_keys_str_mv AT romanvolchenkov th17polarizationunderhypoxiaresultsinincreasedil10productioninapathogenindependentmanner
AT vegardnygaard th17polarizationunderhypoxiaresultsinincreasedil10productioninapathogenindependentmanner
AT zeynepsener th17polarizationunderhypoxiaresultsinincreasedil10productioninapathogenindependentmanner
AT bjørnsteenskalhegg th17polarizationunderhypoxiaresultsinincreasedil10productioninapathogenindependentmanner
_version_ 1725181387049271296