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Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling

Ample evidence pinpoints the phenotypic diversity of blood vessels (BVs) and site-specific functions of their lining endothelial cells (ECs). We harnessed single-cell RNA sequencing (scRNA-seq) to dissect the molecular heterogeneity of blood vascular endothelial cells (BECs) in healthy adult human s...

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Autores principales: He, Yuliang, Tacconi, Carlotta, Dieterich, Lothar C., Kim, Jihye, Restivo, Gaetana, Gousopoulos, Epameinondas, Lindenblatt, Nicole, Levesque, Mitchell P., Claassen, Manfred, Detmar, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997372/
https://www.ncbi.nlm.nih.gov/pubmed/35406678
http://dx.doi.org/10.3390/cells11071111
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author He, Yuliang
Tacconi, Carlotta
Dieterich, Lothar C.
Kim, Jihye
Restivo, Gaetana
Gousopoulos, Epameinondas
Lindenblatt, Nicole
Levesque, Mitchell P.
Claassen, Manfred
Detmar, Michael
author_facet He, Yuliang
Tacconi, Carlotta
Dieterich, Lothar C.
Kim, Jihye
Restivo, Gaetana
Gousopoulos, Epameinondas
Lindenblatt, Nicole
Levesque, Mitchell P.
Claassen, Manfred
Detmar, Michael
author_sort He, Yuliang
collection PubMed
description Ample evidence pinpoints the phenotypic diversity of blood vessels (BVs) and site-specific functions of their lining endothelial cells (ECs). We harnessed single-cell RNA sequencing (scRNA-seq) to dissect the molecular heterogeneity of blood vascular endothelial cells (BECs) in healthy adult human skin and identified six different subpopulations, signifying arterioles, post-arterial capillaries, pre-venular capillaries, post-capillary venules, venules and collecting venules. Individual BEC subtypes exhibited distinctive transcriptomic landscapes associated with diverse biological pathways. These functionally distinct dermal BV segments were characterized by their unique compositions of conventional and novel markers (e.g., arteriole marker GJA5; arteriole capillary markers ASS1 and S100A4; pre-venular capillary markers SOX17 and PLAUR; venular markers EGR2 and LRG1), many of which have been implicated in vascular remodeling upon inflammatory responses. Immunofluorescence staining of human skin sections and whole-mount skin blocks confirmed the discrete expression of these markers along the blood vascular tree in situ, further corroborating BEC heterogeneity in human skin. Overall, our study molecularly refines individual BV compartments, whilst the identification of novel subtype-specific signatures provides more insights for future studies dissecting the responses of distinct vessel segments under pathological conditions.
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spelling pubmed-89973722022-04-12 Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling He, Yuliang Tacconi, Carlotta Dieterich, Lothar C. Kim, Jihye Restivo, Gaetana Gousopoulos, Epameinondas Lindenblatt, Nicole Levesque, Mitchell P. Claassen, Manfred Detmar, Michael Cells Article Ample evidence pinpoints the phenotypic diversity of blood vessels (BVs) and site-specific functions of their lining endothelial cells (ECs). We harnessed single-cell RNA sequencing (scRNA-seq) to dissect the molecular heterogeneity of blood vascular endothelial cells (BECs) in healthy adult human skin and identified six different subpopulations, signifying arterioles, post-arterial capillaries, pre-venular capillaries, post-capillary venules, venules and collecting venules. Individual BEC subtypes exhibited distinctive transcriptomic landscapes associated with diverse biological pathways. These functionally distinct dermal BV segments were characterized by their unique compositions of conventional and novel markers (e.g., arteriole marker GJA5; arteriole capillary markers ASS1 and S100A4; pre-venular capillary markers SOX17 and PLAUR; venular markers EGR2 and LRG1), many of which have been implicated in vascular remodeling upon inflammatory responses. Immunofluorescence staining of human skin sections and whole-mount skin blocks confirmed the discrete expression of these markers along the blood vascular tree in situ, further corroborating BEC heterogeneity in human skin. Overall, our study molecularly refines individual BV compartments, whilst the identification of novel subtype-specific signatures provides more insights for future studies dissecting the responses of distinct vessel segments under pathological conditions. MDPI 2022-03-25 /pmc/articles/PMC8997372/ /pubmed/35406678 http://dx.doi.org/10.3390/cells11071111 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
He, Yuliang
Tacconi, Carlotta
Dieterich, Lothar C.
Kim, Jihye
Restivo, Gaetana
Gousopoulos, Epameinondas
Lindenblatt, Nicole
Levesque, Mitchell P.
Claassen, Manfred
Detmar, Michael
Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling
title Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling
title_full Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling
title_fullStr Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling
title_full_unstemmed Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling
title_short Novel Blood Vascular Endothelial Subtype-Specific Markers in Human Skin Unearthed by Single-Cell Transcriptomic Profiling
title_sort novel blood vascular endothelial subtype-specific markers in human skin unearthed by single-cell transcriptomic profiling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997372/
https://www.ncbi.nlm.nih.gov/pubmed/35406678
http://dx.doi.org/10.3390/cells11071111
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