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T‐cell egress from the thymus: Should I stay or should I go?
T‐cells bearing the αβTCR play a vital role in defending the host against foreign pathogens and malignant transformation of self. Importantly, T‐cells are required to remain tolerant to the host's own cells and tissues in order to prevent self‐reactive responses that can lead to autoimmune dise...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174998/ https://www.ncbi.nlm.nih.gov/pubmed/29485734 http://dx.doi.org/10.1002/JLB.1MR1217-496R |
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author | James, Kieran D. Jenkinson, William E. Anderson, Graham |
author_facet | James, Kieran D. Jenkinson, William E. Anderson, Graham |
author_sort | James, Kieran D. |
collection | PubMed |
description | T‐cells bearing the αβTCR play a vital role in defending the host against foreign pathogens and malignant transformation of self. Importantly, T‐cells are required to remain tolerant to the host's own cells and tissues in order to prevent self‐reactive responses that can lead to autoimmune disease. T‐cells achieve the capacity for self/nonself discrimination by undergoing a highly selective and rigorous developmental program during their maturation in the thymus. This organ is unique in its ability to support a program of T‐cell development that ensures the establishment of a functionally diverse αβTCR repertoire within the peripheral T‐cell pool. The thymus achieves this by virtue of specialized stromal microenvironments that contain heterogeneous cell types, whose organization and function underpins their ability to educate, support, and screen different thymocyte subsets through various stages of development. These stages range from the entry of early T‐cell progenitors into the thymus, through to the positive and negative selection of the αβTCR repertoire. The importance of the thymus medulla as a site for T‐cell tolerance and the exit of newly generated T‐cells into the periphery is well established. In this review, we summarize current knowledge on the developmental pathways that take place during αβT‐cell development in the thymus. In addition, we focus on the mechanisms that regulate thymic egress and contribute to the seeding of peripheral tissues with newly selected self‐tolerant αβT‐cells. |
format | Online Article Text |
id | pubmed-6174998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61749982018-10-15 T‐cell egress from the thymus: Should I stay or should I go? James, Kieran D. Jenkinson, William E. Anderson, Graham J Leukoc Biol Special Focus Issue T‐cells bearing the αβTCR play a vital role in defending the host against foreign pathogens and malignant transformation of self. Importantly, T‐cells are required to remain tolerant to the host's own cells and tissues in order to prevent self‐reactive responses that can lead to autoimmune disease. T‐cells achieve the capacity for self/nonself discrimination by undergoing a highly selective and rigorous developmental program during their maturation in the thymus. This organ is unique in its ability to support a program of T‐cell development that ensures the establishment of a functionally diverse αβTCR repertoire within the peripheral T‐cell pool. The thymus achieves this by virtue of specialized stromal microenvironments that contain heterogeneous cell types, whose organization and function underpins their ability to educate, support, and screen different thymocyte subsets through various stages of development. These stages range from the entry of early T‐cell progenitors into the thymus, through to the positive and negative selection of the αβTCR repertoire. The importance of the thymus medulla as a site for T‐cell tolerance and the exit of newly generated T‐cells into the periphery is well established. In this review, we summarize current knowledge on the developmental pathways that take place during αβT‐cell development in the thymus. In addition, we focus on the mechanisms that regulate thymic egress and contribute to the seeding of peripheral tissues with newly selected self‐tolerant αβT‐cells. John Wiley and Sons Inc. 2018-02-27 2018-08 /pmc/articles/PMC6174998/ /pubmed/29485734 http://dx.doi.org/10.1002/JLB.1MR1217-496R Text en ©2018 The Authors. Society for Leukocyte Biology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Special Focus Issue James, Kieran D. Jenkinson, William E. Anderson, Graham T‐cell egress from the thymus: Should I stay or should I go? |
title | T‐cell egress from the thymus: Should I stay or should I go? |
title_full | T‐cell egress from the thymus: Should I stay or should I go? |
title_fullStr | T‐cell egress from the thymus: Should I stay or should I go? |
title_full_unstemmed | T‐cell egress from the thymus: Should I stay or should I go? |
title_short | T‐cell egress from the thymus: Should I stay or should I go? |
title_sort | t‐cell egress from the thymus: should i stay or should i go? |
topic | Special Focus Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174998/ https://www.ncbi.nlm.nih.gov/pubmed/29485734 http://dx.doi.org/10.1002/JLB.1MR1217-496R |
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