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Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages
Dendritic cells (DCs), monocytes, and macrophages are leukocytes with critical roles in immunity and tolerance. The DC network is evolutionarily conserved; the homologs of human tissue CD141(hi)XCR1(+)CLEC9A(+) DCs and CD1c(+) DCs are murine CD103(+) DCs and CD64(−)CD11b(+) DCs. In addition, human t...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175180/ https://www.ncbi.nlm.nih.gov/pubmed/25200712 http://dx.doi.org/10.1016/j.immuni.2014.08.006 |
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author | McGovern, Naomi Schlitzer, Andreas Gunawan, Merry Jardine, Laura Shin, Amanda Poyner, Elizabeth Green, Kile Dickinson, Rachel Wang, Xiao-nong Low, Donovan Best, Katie Covins, Samuel Milne, Paul Pagan, Sarah Aljefri, Khadija Windebank, Martin Saavedra, Diego Miranda Larbi, Anis Wasan, Pavandip Singh Duan, Kaibo Poidinger, Michael Bigley, Venetia Ginhoux, Florent Collin, Matthew Haniffa, Muzlifah |
author_facet | McGovern, Naomi Schlitzer, Andreas Gunawan, Merry Jardine, Laura Shin, Amanda Poyner, Elizabeth Green, Kile Dickinson, Rachel Wang, Xiao-nong Low, Donovan Best, Katie Covins, Samuel Milne, Paul Pagan, Sarah Aljefri, Khadija Windebank, Martin Saavedra, Diego Miranda Larbi, Anis Wasan, Pavandip Singh Duan, Kaibo Poidinger, Michael Bigley, Venetia Ginhoux, Florent Collin, Matthew Haniffa, Muzlifah |
author_sort | McGovern, Naomi |
collection | PubMed |
description | Dendritic cells (DCs), monocytes, and macrophages are leukocytes with critical roles in immunity and tolerance. The DC network is evolutionarily conserved; the homologs of human tissue CD141(hi)XCR1(+)CLEC9A(+) DCs and CD1c(+) DCs are murine CD103(+) DCs and CD64(−)CD11b(+) DCs. In addition, human tissues also contain CD14(+) cells, currently designated as DCs, with an as-yet unknown murine counterpart. Here we have demonstrated that human dermal CD14(+) cells are a tissue-resident population of monocyte-derived macrophages with a short half-life of <6 days. The decline and reconstitution kinetics of human blood CD14(+) monocytes and dermal CD14(+) cells in vivo supported their precursor-progeny relationship. The murine homologs of human dermal CD14(+) cells are CD11b(+)CD64(+) monocyte-derived macrophages. Human and mouse monocytes and macrophages were defined by highly conserved gene transcripts, which were distinct from DCs. The demonstration of monocyte-derived macrophages in the steady state in human tissue supports a conserved organization of human and mouse mononuclear phagocyte system. |
format | Online Article Text |
id | pubmed-4175180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41751802014-09-30 Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages McGovern, Naomi Schlitzer, Andreas Gunawan, Merry Jardine, Laura Shin, Amanda Poyner, Elizabeth Green, Kile Dickinson, Rachel Wang, Xiao-nong Low, Donovan Best, Katie Covins, Samuel Milne, Paul Pagan, Sarah Aljefri, Khadija Windebank, Martin Saavedra, Diego Miranda Larbi, Anis Wasan, Pavandip Singh Duan, Kaibo Poidinger, Michael Bigley, Venetia Ginhoux, Florent Collin, Matthew Haniffa, Muzlifah Immunity Article Dendritic cells (DCs), monocytes, and macrophages are leukocytes with critical roles in immunity and tolerance. The DC network is evolutionarily conserved; the homologs of human tissue CD141(hi)XCR1(+)CLEC9A(+) DCs and CD1c(+) DCs are murine CD103(+) DCs and CD64(−)CD11b(+) DCs. In addition, human tissues also contain CD14(+) cells, currently designated as DCs, with an as-yet unknown murine counterpart. Here we have demonstrated that human dermal CD14(+) cells are a tissue-resident population of monocyte-derived macrophages with a short half-life of <6 days. The decline and reconstitution kinetics of human blood CD14(+) monocytes and dermal CD14(+) cells in vivo supported their precursor-progeny relationship. The murine homologs of human dermal CD14(+) cells are CD11b(+)CD64(+) monocyte-derived macrophages. Human and mouse monocytes and macrophages were defined by highly conserved gene transcripts, which were distinct from DCs. The demonstration of monocyte-derived macrophages in the steady state in human tissue supports a conserved organization of human and mouse mononuclear phagocyte system. Cell Press 2014-09-18 /pmc/articles/PMC4175180/ /pubmed/25200712 http://dx.doi.org/10.1016/j.immuni.2014.08.006 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Article McGovern, Naomi Schlitzer, Andreas Gunawan, Merry Jardine, Laura Shin, Amanda Poyner, Elizabeth Green, Kile Dickinson, Rachel Wang, Xiao-nong Low, Donovan Best, Katie Covins, Samuel Milne, Paul Pagan, Sarah Aljefri, Khadija Windebank, Martin Saavedra, Diego Miranda Larbi, Anis Wasan, Pavandip Singh Duan, Kaibo Poidinger, Michael Bigley, Venetia Ginhoux, Florent Collin, Matthew Haniffa, Muzlifah Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages |
title | Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages |
title_full | Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages |
title_fullStr | Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages |
title_full_unstemmed | Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages |
title_short | Human Dermal CD14(+) Cells Are a Transient Population of Monocyte-Derived Macrophages |
title_sort | human dermal cd14(+) cells are a transient population of monocyte-derived macrophages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175180/ https://www.ncbi.nlm.nih.gov/pubmed/25200712 http://dx.doi.org/10.1016/j.immuni.2014.08.006 |
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