Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine
DC Field | Value | Language |
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dc.contributor.author | Jaeu Yi | - |
dc.contributor.author | Jisun Jung | - |
dc.contributor.author | Daehee Han | - |
dc.contributor.author | Charles D. Surh | - |
dc.contributor.author | You Jeong Lee | - |
dc.date.available | 2019-08-19T02:07:03Z | - |
dc.date.created | 2019-04-22 | - |
dc.date.issued | 2019-03 | - |
dc.identifier.issn | 1016-8478 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/6015 | - |
dc.description.abstract | CD4 T cells differentiate into ROR gamma t/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 naive 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 naive 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. C.The Korean Society for Molecular and Cellular Biology. All rights reserved. | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | KOREAN SOC MOLECULAR & CELLULAR BIOLOGY | - |
dc.subject | antigen-specific CD4 T cells | - |
dc.subject | germ-free mice | - |
dc.subject | segmented filamentous bacteria | - |
dc.subject | single cell RT-PCR | - |
dc.subject | small intestine | - |
dc.title | Segmented Filamentous Bacteria Induce Divergent Populations of Antigen-Specific CD4 T Cells in the Small Intestine | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000462739200005 | - |
dc.identifier.scopusid | 2-s2.0-85063997285 | - |
dc.identifier.rimsid | 67879 | - |
dc.contributor.affiliatedAuthor | Jaeu Yi | - |
dc.contributor.affiliatedAuthor | Jisun Jung | - |
dc.contributor.affiliatedAuthor | Daehee Han | - |
dc.contributor.affiliatedAuthor | Charles D. Surh | - |
dc.contributor.affiliatedAuthor | You Jeong Lee | - |
dc.identifier.doi | 10.14348/molcells.2018.0424 | - |
dc.identifier.bibliographicCitation | MOLECULES AND CELLS, v.42, no.3, pp.228 - 236 | - |
dc.citation.title | MOLECULES AND CELLS | - |
dc.citation.volume | 42 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 228 | - |
dc.citation.endPage | 236 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.subject.keywordPlus | MICROBIOTA | - |
dc.subject.keywordPlus | DIFFERENTIATION | - |
dc.subject.keywordPlus | IMMUNITY | - |
dc.subject.keywordPlus | MICE | - |
dc.subject.keywordPlus | TH1 | - |
dc.subject.keywordAuthor | antigen-specific CD4 T cells | - |
dc.subject.keywordAuthor | germ-free mice | - |
dc.subject.keywordAuthor | segmented filamentous bacteria | - |
dc.subject.keywordAuthor | single cell RT-PCR | - |
dc.subject.keywordAuthor | small intestine | - |