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A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels

Dendritic cells (DCs), macrophages (Mφ), and T cells are major components of the skin immune system, but their interstitial spatial organization is poorly characterized. Using four-channel whole-mount immunofluorescence staining of the human dermis, we demonstrated the three-dimensional distribution...

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Autores principales: Wang, Xiao-Nong, McGovern, Naomi, Gunawan, Merry, Richardson, Connor, Windebank, Martin, Siah, Tee-Wei, Lim, Hwee-Ying, Fink, Katja, Li, Jackson L Yao, Ng, Lai G, Ginhoux, Florent, Angeli, Veronique, Collin, Matthew, Haniffa, Muzlifah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961477/
https://www.ncbi.nlm.nih.gov/pubmed/24352044
http://dx.doi.org/10.1038/jid.2013.481
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author Wang, Xiao-Nong
McGovern, Naomi
Gunawan, Merry
Richardson, Connor
Windebank, Martin
Siah, Tee-Wei
Lim, Hwee-Ying
Fink, Katja
Li, Jackson L Yao
Ng, Lai G
Ginhoux, Florent
Angeli, Veronique
Collin, Matthew
Haniffa, Muzlifah
author_facet Wang, Xiao-Nong
McGovern, Naomi
Gunawan, Merry
Richardson, Connor
Windebank, Martin
Siah, Tee-Wei
Lim, Hwee-Ying
Fink, Katja
Li, Jackson L Yao
Ng, Lai G
Ginhoux, Florent
Angeli, Veronique
Collin, Matthew
Haniffa, Muzlifah
author_sort Wang, Xiao-Nong
collection PubMed
description Dendritic cells (DCs), macrophages (Mφ), and T cells are major components of the skin immune system, but their interstitial spatial organization is poorly characterized. Using four-channel whole-mount immunofluorescence staining of the human dermis, we demonstrated the three-dimensional distribution of CD31(+) blood capillaries, LYVE-1(+) lymphatics, discrete populations of CD11c(+) myeloid DCs, FXIIIa(+) Mφ, and lymphocytes. We showed phenotypic and morphological differences in situ between DCs and Mφ. DCs formed the first dermal cellular layer (0–20 μm beneath the dermoepidermal junction), Mφ were located deeper (40–60 μm), and CD3(+) lymphocytes were observed throughout (0–60 μm). Below this level, DCs, T cells, and the majority of Mφ formed stable perivascular sheaths. Whole-mount imaging revealed the true extent of dermal leukocytes previously underestimated from cross-section views. The total area of apical dermis (0–30 μm) contained approximately 10-fold more myeloid DCs than the entire blood volume of an average individual. Surprisingly, <1% of dermal DCs occupied lymphatics in freshly isolated skin. Dermal DCs rapidly accumulated within lymphatics, but Mφ remained fixed in skin explants cultured ex vivo. The leukocyte architecture observed in normal skin was distorted in inflammation and disease. These studies illustrate the micro-anatomy of dermal leukocytes and provide further insights into their functional organization.
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spelling pubmed-39614772014-03-24 A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels Wang, Xiao-Nong McGovern, Naomi Gunawan, Merry Richardson, Connor Windebank, Martin Siah, Tee-Wei Lim, Hwee-Ying Fink, Katja Li, Jackson L Yao Ng, Lai G Ginhoux, Florent Angeli, Veronique Collin, Matthew Haniffa, Muzlifah J Invest Dermatol Original Article Dendritic cells (DCs), macrophages (Mφ), and T cells are major components of the skin immune system, but their interstitial spatial organization is poorly characterized. Using four-channel whole-mount immunofluorescence staining of the human dermis, we demonstrated the three-dimensional distribution of CD31(+) blood capillaries, LYVE-1(+) lymphatics, discrete populations of CD11c(+) myeloid DCs, FXIIIa(+) Mφ, and lymphocytes. We showed phenotypic and morphological differences in situ between DCs and Mφ. DCs formed the first dermal cellular layer (0–20 μm beneath the dermoepidermal junction), Mφ were located deeper (40–60 μm), and CD3(+) lymphocytes were observed throughout (0–60 μm). Below this level, DCs, T cells, and the majority of Mφ formed stable perivascular sheaths. Whole-mount imaging revealed the true extent of dermal leukocytes previously underestimated from cross-section views. The total area of apical dermis (0–30 μm) contained approximately 10-fold more myeloid DCs than the entire blood volume of an average individual. Surprisingly, <1% of dermal DCs occupied lymphatics in freshly isolated skin. Dermal DCs rapidly accumulated within lymphatics, but Mφ remained fixed in skin explants cultured ex vivo. The leukocyte architecture observed in normal skin was distorted in inflammation and disease. These studies illustrate the micro-anatomy of dermal leukocytes and provide further insights into their functional organization. Nature Publishing Group 2014-04 2013-12-19 /pmc/articles/PMC3961477/ /pubmed/24352044 http://dx.doi.org/10.1038/jid.2013.481 Text en Copyright © 2014 The Society for Investigative Dermatology, Inc http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Wang, Xiao-Nong
McGovern, Naomi
Gunawan, Merry
Richardson, Connor
Windebank, Martin
Siah, Tee-Wei
Lim, Hwee-Ying
Fink, Katja
Li, Jackson L Yao
Ng, Lai G
Ginhoux, Florent
Angeli, Veronique
Collin, Matthew
Haniffa, Muzlifah
A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels
title A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels
title_full A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels
title_fullStr A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels
title_full_unstemmed A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels
title_short A Three-Dimensional Atlas of Human Dermal Leukocytes, Lymphatics, and Blood Vessels
title_sort three-dimensional atlas of human dermal leukocytes, lymphatics, and blood vessels
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961477/
https://www.ncbi.nlm.nih.gov/pubmed/24352044
http://dx.doi.org/10.1038/jid.2013.481
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