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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2014
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.
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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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