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Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels
Characterising the longevity of immunological memory requires establishing the rules underlying the renewal and death of peripheral T cells. However, we lack knowledge of the population structure and how self-renewal and de novo influx contribute to the maintenance of memory compartments. Here, we c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426903/ https://www.ncbi.nlm.nih.gov/pubmed/28282024 http://dx.doi.org/10.7554/eLife.23013 |
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author | Gossel, Graeme Hogan, Thea Cownden, Daniel Seddon, Benedict Yates, Andrew J |
author_facet | Gossel, Graeme Hogan, Thea Cownden, Daniel Seddon, Benedict Yates, Andrew J |
author_sort | Gossel, Graeme |
collection | PubMed |
description | Characterising the longevity of immunological memory requires establishing the rules underlying the renewal and death of peripheral T cells. However, we lack knowledge of the population structure and how self-renewal and de novo influx contribute to the maintenance of memory compartments. Here, we characterise the kinetics and structure of murine CD4 T cell memory subsets by measuring the rates of influx of new cells and using detailed timecourses of DNA labelling that also distinguish the behaviour of recently divided and quiescent cells. We find that both effector and central memory CD4 T cells comprise subpopulations with highly divergent rates of turnover, and show that inflows of new cells sourced from the naive pool strongly impact estimates of memory cell lifetimes and division rates. We also demonstrate that the maintenance of CD4 T cell memory subsets in healthy mice is unexpectedly and strikingly reliant on this replenishment. DOI: http://dx.doi.org/10.7554/eLife.23013.001 |
format | Online Article Text |
id | pubmed-5426903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54269032017-05-15 Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels Gossel, Graeme Hogan, Thea Cownden, Daniel Seddon, Benedict Yates, Andrew J eLife Computational and Systems Biology Characterising the longevity of immunological memory requires establishing the rules underlying the renewal and death of peripheral T cells. However, we lack knowledge of the population structure and how self-renewal and de novo influx contribute to the maintenance of memory compartments. Here, we characterise the kinetics and structure of murine CD4 T cell memory subsets by measuring the rates of influx of new cells and using detailed timecourses of DNA labelling that also distinguish the behaviour of recently divided and quiescent cells. We find that both effector and central memory CD4 T cells comprise subpopulations with highly divergent rates of turnover, and show that inflows of new cells sourced from the naive pool strongly impact estimates of memory cell lifetimes and division rates. We also demonstrate that the maintenance of CD4 T cell memory subsets in healthy mice is unexpectedly and strikingly reliant on this replenishment. DOI: http://dx.doi.org/10.7554/eLife.23013.001 eLife Sciences Publications, Ltd 2017-03-10 /pmc/articles/PMC5426903/ /pubmed/28282024 http://dx.doi.org/10.7554/eLife.23013 Text en © 2017, Gossel et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Gossel, Graeme Hogan, Thea Cownden, Daniel Seddon, Benedict Yates, Andrew J Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels |
title | Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels |
title_full | Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels |
title_fullStr | Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels |
title_full_unstemmed | Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels |
title_short | Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels |
title_sort | memory cd4 t cell subsets are kinetically heterogeneous and replenished from naive t cells at high levels |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426903/ https://www.ncbi.nlm.nih.gov/pubmed/28282024 http://dx.doi.org/10.7554/eLife.23013 |
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