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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....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2017
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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. |
format | Online Article Text |
id | pubmed-5502436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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