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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...

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Autores principales: Gossel, Graeme, Hogan, Thea, Cownden, Daniel, Seddon, Benedict, Yates, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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
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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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