Cargando…

Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine

CD4 T cells differentiate into RORγt/IL-17A-expressing cells in the small intestine following colonization by segmented filamentous bacteria (SFB). However, it remains unclear whether SFB-specific CD4 T cells can differentiate directly from naïve precursors, and whether their effector differentiatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Yi, Jaeu, Jung, Jisun, Han, Daehee, Surh, Charles D., Lee, You Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449712/
https://www.ncbi.nlm.nih.gov/pubmed/30759969
http://dx.doi.org/10.14348/molcells.2018.0424
_version_ 1783408907565137920
author Yi, Jaeu
Jung, Jisun
Han, Daehee
Surh, Charles D.
Lee, You Jeong
author_facet Yi, Jaeu
Jung, Jisun
Han, Daehee
Surh, Charles D.
Lee, You Jeong
author_sort Yi, Jaeu
collection PubMed
description CD4 T cells differentiate into RORγt/IL-17A-expressing cells in the small intestine following colonization by segmented filamentous bacteria (SFB). However, it remains unclear whether SFB-specific CD4 T cells can differentiate directly from naïve precursors, and whether their effector differentiation is solely directed towards the Th17 lineage. In this study, we used adoptive T cell transfer experiments and showed that naïve CD4 T cells can migrate to the small intestinal lamina propria (sLP) and differentiate into effector T cells that synthesize IL-17A in response to SFB colonization. Using single cell RT-PCR analysis, we showed that the progenies of SFB responding T cells are not uniform but composed of transcriptionally divergent populations including Th1, Th17 and follicular helper T cells. We further confirmed this finding using in vitro culture of SFB specific intestinal CD4 T cells in the presence of cognate antigens, which also generated heterogeneous population with similar features. Collectively, these findings indicate that a single species of intestinal bacteria can generate a divergent population of antigen-specific effector CD4 T cells, rather than it provides a cytokine milieu for the development of a particular effector T cell subset.
format Online
Article
Text
id pubmed-6449712
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Korean Society for Molecular and Cellular Biology
record_format MEDLINE/PubMed
spelling pubmed-64497122019-04-10 Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine Yi, Jaeu Jung, Jisun Han, Daehee Surh, Charles D. Lee, You Jeong Mol Cells Article CD4 T cells differentiate into RORγt/IL-17A-expressing cells in the small intestine following colonization by segmented filamentous bacteria (SFB). However, it remains unclear whether SFB-specific CD4 T cells can differentiate directly from naïve precursors, and whether their effector differentiation is solely directed towards the Th17 lineage. In this study, we used adoptive T cell transfer experiments and showed that naïve CD4 T cells can migrate to the small intestinal lamina propria (sLP) and differentiate into effector T cells that synthesize IL-17A in response to SFB colonization. Using single cell RT-PCR analysis, we showed that the progenies of SFB responding T cells are not uniform but composed of transcriptionally divergent populations including Th1, Th17 and follicular helper T cells. We further confirmed this finding using in vitro culture of SFB specific intestinal CD4 T cells in the presence of cognate antigens, which also generated heterogeneous population with similar features. Collectively, these findings indicate that a single species of intestinal bacteria can generate a divergent population of antigen-specific effector CD4 T cells, rather than it provides a cytokine milieu for the development of a particular effector T cell subset. Korean Society for Molecular and Cellular Biology 2019-03-31 2019-02-08 /pmc/articles/PMC6449712/ /pubmed/30759969 http://dx.doi.org/10.14348/molcells.2018.0424 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.
spellingShingle Article
Yi, Jaeu
Jung, Jisun
Han, Daehee
Surh, Charles D.
Lee, You Jeong
Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine
title Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine
title_full Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine
title_fullStr Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine
title_full_unstemmed Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine
title_short Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine
title_sort segmented filamentous bacteria induce divergent populations of antigen-specific cd4 t cells in the small intestine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449712/
https://www.ncbi.nlm.nih.gov/pubmed/30759969
http://dx.doi.org/10.14348/molcells.2018.0424
work_keys_str_mv AT yijaeu segmentedfilamentousbacteriainducedivergentpopulationsofantigenspecificcd4tcellsinthesmallintestine
AT jungjisun segmentedfilamentousbacteriainducedivergentpopulationsofantigenspecificcd4tcellsinthesmallintestine
AT handaehee segmentedfilamentousbacteriainducedivergentpopulationsofantigenspecificcd4tcellsinthesmallintestine
AT surhcharlesd segmentedfilamentousbacteriainducedivergentpopulationsofantigenspecificcd4tcellsinthesmallintestine
AT leeyoujeong segmentedfilamentousbacteriainducedivergentpopulationsofantigenspecificcd4tcellsinthesmallintestine