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Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells
Analysis of the T-cell receptor (TCR) repertoire of innate CD4(+) T cells selected by major histocompatibility complex (MHC) class II-dependent thymocyte–thymocyte (T-T) interaction (T-T CD4(+) T cells) is essential for predicting the characteristics of the antigens that bind to these T cells and fo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351420/ https://www.ncbi.nlm.nih.gov/pubmed/25813222 http://dx.doi.org/10.1038/emm.2015.7 |
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author | Kang, Byung Hyun Min, Hye Sook Lee, You Jeong Choi, Bomi Kim, Eun Ji Lee, Jonghoon Kim, Jeong-Rae Cho, Kwang-Hyun Kim, Tae Jin Jung, Kyeong Cheon Park, Seong Hoe |
author_facet | Kang, Byung Hyun Min, Hye Sook Lee, You Jeong Choi, Bomi Kim, Eun Ji Lee, Jonghoon Kim, Jeong-Rae Cho, Kwang-Hyun Kim, Tae Jin Jung, Kyeong Cheon Park, Seong Hoe |
author_sort | Kang, Byung Hyun |
collection | PubMed |
description | Analysis of the T-cell receptor (TCR) repertoire of innate CD4(+) T cells selected by major histocompatibility complex (MHC) class II-dependent thymocyte–thymocyte (T-T) interaction (T-T CD4(+) T cells) is essential for predicting the characteristics of the antigens that bind to these T cells and for distinguishing T-T CD4(+) T cells from other types of innate T cells. Using the TCR(mini) Tg mouse model, we show that the repertoire of TCRα chains in T-T CD4(+) T cells was extremely diverse, in contrast to the repertoires previously described for other types of innate T cells. The TCRα chain sequences significantly overlapped between T-T CD4(+) T cells and conventional CD4(+) T cells in the thymus and spleen. However, the diversity of the TCRα repertoire of T-T CD4(+) T cells seemed to be restricted compared with that of conventional CD4(+) T cells. Interestingly, the frequency of the parental OT-II TCRα chains was significantly reduced in the process of T-T interaction. This diverse and shifted repertoire in T-T CD4(+) T cells has biological relevance in terms of defense against diverse pathogens and a possible regulatory role during peripheral T-T interaction. |
format | Online Article Text |
id | pubmed-4351420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43514202015-03-10 Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells Kang, Byung Hyun Min, Hye Sook Lee, You Jeong Choi, Bomi Kim, Eun Ji Lee, Jonghoon Kim, Jeong-Rae Cho, Kwang-Hyun Kim, Tae Jin Jung, Kyeong Cheon Park, Seong Hoe Exp Mol Med Original Article Analysis of the T-cell receptor (TCR) repertoire of innate CD4(+) T cells selected by major histocompatibility complex (MHC) class II-dependent thymocyte–thymocyte (T-T) interaction (T-T CD4(+) T cells) is essential for predicting the characteristics of the antigens that bind to these T cells and for distinguishing T-T CD4(+) T cells from other types of innate T cells. Using the TCR(mini) Tg mouse model, we show that the repertoire of TCRα chains in T-T CD4(+) T cells was extremely diverse, in contrast to the repertoires previously described for other types of innate T cells. The TCRα chain sequences significantly overlapped between T-T CD4(+) T cells and conventional CD4(+) T cells in the thymus and spleen. However, the diversity of the TCRα repertoire of T-T CD4(+) T cells seemed to be restricted compared with that of conventional CD4(+) T cells. Interestingly, the frequency of the parental OT-II TCRα chains was significantly reduced in the process of T-T interaction. This diverse and shifted repertoire in T-T CD4(+) T cells has biological relevance in terms of defense against diverse pathogens and a possible regulatory role during peripheral T-T interaction. Nature Publishing Group 2015-03 2015-03-27 /pmc/articles/PMC4351420/ /pubmed/25813222 http://dx.doi.org/10.1038/emm.2015.7 Text en Copyright © 2015 KSBMB. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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-nc-nd/4.0/ |
spellingShingle | Original Article Kang, Byung Hyun Min, Hye Sook Lee, You Jeong Choi, Bomi Kim, Eun Ji Lee, Jonghoon Kim, Jeong-Rae Cho, Kwang-Hyun Kim, Tae Jin Jung, Kyeong Cheon Park, Seong Hoe Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells |
title | Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells |
title_full | Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells |
title_fullStr | Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells |
title_full_unstemmed | Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells |
title_short | Analyses of the TCR repertoire of MHC class II-restricted innate CD4(+) T cells |
title_sort | analyses of the tcr repertoire of mhc class ii-restricted innate cd4(+) t cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351420/ https://www.ncbi.nlm.nih.gov/pubmed/25813222 http://dx.doi.org/10.1038/emm.2015.7 |
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