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The fate and lifespan of human monocyte subsets in steady state and systemic inflammation

In humans, the monocyte pool comprises three subsets (classical, intermediate, and nonclassical) that circulate in dynamic equilibrium. The kinetics underlying their generation, differentiation, and disappearance are critical to understanding both steady-state homeostasis and inflammatory responses....

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Autores principales: Patel, Amit A., Zhang, Yan, Fullerton, James N., Boelen, Lies, Rongvaux, Anthony, Maini, Alexander A., Bigley, Venetia, Flavell, Richard A., Gilroy, Derek W., Asquith, Becca, Macallan, Derek, Yona, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502436/
https://www.ncbi.nlm.nih.gov/pubmed/28606987
http://dx.doi.org/10.1084/jem.20170355
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author Patel, Amit A.
Zhang, Yan
Fullerton, James N.
Boelen, Lies
Rongvaux, Anthony
Maini, Alexander A.
Bigley, Venetia
Flavell, Richard A.
Gilroy, Derek W.
Asquith, Becca
Macallan, Derek
Yona, Simon
author_facet Patel, Amit A.
Zhang, Yan
Fullerton, James N.
Boelen, Lies
Rongvaux, Anthony
Maini, Alexander A.
Bigley, Venetia
Flavell, Richard A.
Gilroy, Derek W.
Asquith, Becca
Macallan, Derek
Yona, Simon
author_sort Patel, Amit A.
collection PubMed
description In humans, the monocyte pool comprises three subsets (classical, intermediate, and nonclassical) that circulate in dynamic equilibrium. The kinetics underlying their generation, differentiation, and disappearance are critical to understanding both steady-state homeostasis and inflammatory responses. Here, using human in vivo deuterium labeling, we demonstrate that classical monocytes emerge first from marrow, after a postmitotic interval of 1.6 d, and circulate for a day. Subsequent labeling of intermediate and nonclassical monocytes is consistent with a model of sequential transition. Intermediate and nonclassical monocytes have longer circulating lifespans (∼4 and ∼7 d, respectively). In a human experimental endotoxemia model, a transient but profound monocytopenia was observed; restoration of circulating monocytes was achieved by the early release of classical monocytes from bone marrow. The sequence of repopulation recapitulated the order of maturation in healthy homeostasis. This developmental relationship between monocyte subsets was verified by fate mapping grafted human classical monocytes into humanized mice, which were able to differentiate sequentially into intermediate and nonclassical cells.
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spelling pubmed-55024362017-07-10 The fate and lifespan of human monocyte subsets in steady state and systemic inflammation Patel, Amit A. Zhang, Yan Fullerton, James N. Boelen, Lies Rongvaux, Anthony Maini, Alexander A. Bigley, Venetia Flavell, Richard A. Gilroy, Derek W. Asquith, Becca Macallan, Derek Yona, Simon J Exp Med Research Articles In humans, the monocyte pool comprises three subsets (classical, intermediate, and nonclassical) that circulate in dynamic equilibrium. The kinetics underlying their generation, differentiation, and disappearance are critical to understanding both steady-state homeostasis and inflammatory responses. Here, using human in vivo deuterium labeling, we demonstrate that classical monocytes emerge first from marrow, after a postmitotic interval of 1.6 d, and circulate for a day. Subsequent labeling of intermediate and nonclassical monocytes is consistent with a model of sequential transition. Intermediate and nonclassical monocytes have longer circulating lifespans (∼4 and ∼7 d, respectively). In a human experimental endotoxemia model, a transient but profound monocytopenia was observed; restoration of circulating monocytes was achieved by the early release of classical monocytes from bone marrow. The sequence of repopulation recapitulated the order of maturation in healthy homeostasis. This developmental relationship between monocyte subsets was verified by fate mapping grafted human classical monocytes into humanized mice, which were able to differentiate sequentially into intermediate and nonclassical cells. The Rockefeller University Press 2017-07-03 /pmc/articles/PMC5502436/ /pubmed/28606987 http://dx.doi.org/10.1084/jem.20170355 Text en © 2017 Patel et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Patel, Amit A.
Zhang, Yan
Fullerton, James N.
Boelen, Lies
Rongvaux, Anthony
Maini, Alexander A.
Bigley, Venetia
Flavell, Richard A.
Gilroy, Derek W.
Asquith, Becca
Macallan, Derek
Yona, Simon
The fate and lifespan of human monocyte subsets in steady state and systemic inflammation
title The fate and lifespan of human monocyte subsets in steady state and systemic inflammation
title_full The fate and lifespan of human monocyte subsets in steady state and systemic inflammation
title_fullStr The fate and lifespan of human monocyte subsets in steady state and systemic inflammation
title_full_unstemmed The fate and lifespan of human monocyte subsets in steady state and systemic inflammation
title_short The fate and lifespan of human monocyte subsets in steady state and systemic inflammation
title_sort fate and lifespan of human monocyte subsets in steady state and systemic inflammation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502436/
https://www.ncbi.nlm.nih.gov/pubmed/28606987
http://dx.doi.org/10.1084/jem.20170355
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