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Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8
Regulation of intestinal T-cell responses is crucial for immune homeostasis and prevention of inflammatory bowel disease (IBD). A vital cytokine in regulating intestinal Tcells is transforming growth factor-β (TGFβ), which is secreted by cells as a latent complex that requires activation to function...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439516/ https://www.ncbi.nlm.nih.gov/pubmed/27782111 http://dx.doi.org/10.1038/mi.2016.94 |
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author | Fenton, TM Kelly, A Shuttleworth, EE Smedley, C Atakilit, A Powrie, F Campbell, S Nishimura, SL Sheppard, D Levison, S Worthington, JJ Lehtinen, MJ Travis, MA |
author_facet | Fenton, TM Kelly, A Shuttleworth, EE Smedley, C Atakilit, A Powrie, F Campbell, S Nishimura, SL Sheppard, D Levison, S Worthington, JJ Lehtinen, MJ Travis, MA |
author_sort | Fenton, TM |
collection | PubMed |
description | Regulation of intestinal T-cell responses is crucial for immune homeostasis and prevention of inflammatory bowel disease (IBD). A vital cytokine in regulating intestinal Tcells is transforming growth factor-β (TGFβ), which is secreted by cells as a latent complex that requires activation to function. However, how TGFβ activation is regulated in the human intestine, and how such pathways are altered in IBD is completely unknown. Here we show that a key activator of TGFβ, integrin αvβ8, is highly expressed on human intestinal dendritic cells (DCs), specifically on the CD1c(+) but not the CD141(+) intestinal DC subset. Expression was significantly upregulated on intestinal DC from IBD patients, indicating that inflammatory signals may upregulate expression of this key TGFβ-activating molecule. Indeed, we found that the Toll-like receptor 4 ligand lipopolysaccharide upregulates integrin αvβ8 expression and TGFβ activation by human DC. We also show that DC expression of integrin αvβ8 enhanced induction of FOXP3 in CD4(+) Tcells, suggesting functional importance of integrin αvβ8 expression by human DC. These results show that microbial signals enhance the TGFβ-activating ability of human DC via regulation of integrin αvβ8 expression, and that intestinal inflammation may drive this pathway in patients with IBD. |
format | Online Article Text |
id | pubmed-5439516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-54395162017-05-22 Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 Fenton, TM Kelly, A Shuttleworth, EE Smedley, C Atakilit, A Powrie, F Campbell, S Nishimura, SL Sheppard, D Levison, S Worthington, JJ Lehtinen, MJ Travis, MA Mucosal Immunol Article Regulation of intestinal T-cell responses is crucial for immune homeostasis and prevention of inflammatory bowel disease (IBD). A vital cytokine in regulating intestinal Tcells is transforming growth factor-β (TGFβ), which is secreted by cells as a latent complex that requires activation to function. However, how TGFβ activation is regulated in the human intestine, and how such pathways are altered in IBD is completely unknown. Here we show that a key activator of TGFβ, integrin αvβ8, is highly expressed on human intestinal dendritic cells (DCs), specifically on the CD1c(+) but not the CD141(+) intestinal DC subset. Expression was significantly upregulated on intestinal DC from IBD patients, indicating that inflammatory signals may upregulate expression of this key TGFβ-activating molecule. Indeed, we found that the Toll-like receptor 4 ligand lipopolysaccharide upregulates integrin αvβ8 expression and TGFβ activation by human DC. We also show that DC expression of integrin αvβ8 enhanced induction of FOXP3 in CD4(+) Tcells, suggesting functional importance of integrin αvβ8 expression by human DC. These results show that microbial signals enhance the TGFβ-activating ability of human DC via regulation of integrin αvβ8 expression, and that intestinal inflammation may drive this pathway in patients with IBD. 2016-10-26 2017-05 /pmc/articles/PMC5439516/ /pubmed/27782111 http://dx.doi.org/10.1038/mi.2016.94 Text en http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fenton, TM Kelly, A Shuttleworth, EE Smedley, C Atakilit, A Powrie, F Campbell, S Nishimura, SL Sheppard, D Levison, S Worthington, JJ Lehtinen, MJ Travis, MA Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 |
title | Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 |
title_full | Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 |
title_fullStr | Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 |
title_full_unstemmed | Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 |
title_short | Inflammatory cues enhance TGFβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 |
title_sort | inflammatory cues enhance tgfβ activation by distinct subsets of human intestinal dendritic cells via integrin αvβ8 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439516/ https://www.ncbi.nlm.nih.gov/pubmed/27782111 http://dx.doi.org/10.1038/mi.2016.94 |
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