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Dual function of perivascular fibroblasts in vascular stabilization in zebrafish

Blood vessels are vital to sustain life in all vertebrates. While it is known that mural cells (pericytes and smooth muscle cells) regulate vascular integrity, the contribution of other cell types to vascular stabilization has been largely unexplored. Using zebrafish, we identified sclerotome-derive...

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Autores principales: Rajan, Arsheen M., Ma, Roger C., Kocha, Katrinka M., Zhang, Dan J., Huang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644104/
https://www.ncbi.nlm.nih.gov/pubmed/33104690
http://dx.doi.org/10.1371/journal.pgen.1008800
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author Rajan, Arsheen M.
Ma, Roger C.
Kocha, Katrinka M.
Zhang, Dan J.
Huang, Peng
author_facet Rajan, Arsheen M.
Ma, Roger C.
Kocha, Katrinka M.
Zhang, Dan J.
Huang, Peng
author_sort Rajan, Arsheen M.
collection PubMed
description Blood vessels are vital to sustain life in all vertebrates. While it is known that mural cells (pericytes and smooth muscle cells) regulate vascular integrity, the contribution of other cell types to vascular stabilization has been largely unexplored. Using zebrafish, we identified sclerotome-derived perivascular fibroblasts as a novel population of blood vessel associated cells. In contrast to pericytes, perivascular fibroblasts emerge early during development, express the extracellular matrix (ECM) genes col1a2 and col5a1, and display distinct morphology and distribution. Time-lapse imaging reveals that perivascular fibroblasts serve as pericyte precursors. Genetic ablation of perivascular fibroblasts markedly reduces collagen deposition around endothelial cells, resulting in dysmorphic blood vessels with variable diameters. Strikingly, col5a1 mutants show spontaneous hemorrhage, and the penetrance of the phenotype is strongly enhanced by the additional loss of col1a2. Together, our work reveals dual roles of perivascular fibroblasts in vascular stabilization where they establish the ECM around nascent vessels and function as pericyte progenitors.
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spelling pubmed-76441042020-11-16 Dual function of perivascular fibroblasts in vascular stabilization in zebrafish Rajan, Arsheen M. Ma, Roger C. Kocha, Katrinka M. Zhang, Dan J. Huang, Peng PLoS Genet Research Article Blood vessels are vital to sustain life in all vertebrates. While it is known that mural cells (pericytes and smooth muscle cells) regulate vascular integrity, the contribution of other cell types to vascular stabilization has been largely unexplored. Using zebrafish, we identified sclerotome-derived perivascular fibroblasts as a novel population of blood vessel associated cells. In contrast to pericytes, perivascular fibroblasts emerge early during development, express the extracellular matrix (ECM) genes col1a2 and col5a1, and display distinct morphology and distribution. Time-lapse imaging reveals that perivascular fibroblasts serve as pericyte precursors. Genetic ablation of perivascular fibroblasts markedly reduces collagen deposition around endothelial cells, resulting in dysmorphic blood vessels with variable diameters. Strikingly, col5a1 mutants show spontaneous hemorrhage, and the penetrance of the phenotype is strongly enhanced by the additional loss of col1a2. Together, our work reveals dual roles of perivascular fibroblasts in vascular stabilization where they establish the ECM around nascent vessels and function as pericyte progenitors. Public Library of Science 2020-10-26 /pmc/articles/PMC7644104/ /pubmed/33104690 http://dx.doi.org/10.1371/journal.pgen.1008800 Text en © 2020 Rajan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rajan, Arsheen M.
Ma, Roger C.
Kocha, Katrinka M.
Zhang, Dan J.
Huang, Peng
Dual function of perivascular fibroblasts in vascular stabilization in zebrafish
title Dual function of perivascular fibroblasts in vascular stabilization in zebrafish
title_full Dual function of perivascular fibroblasts in vascular stabilization in zebrafish
title_fullStr Dual function of perivascular fibroblasts in vascular stabilization in zebrafish
title_full_unstemmed Dual function of perivascular fibroblasts in vascular stabilization in zebrafish
title_short Dual function of perivascular fibroblasts in vascular stabilization in zebrafish
title_sort dual function of perivascular fibroblasts in vascular stabilization in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644104/
https://www.ncbi.nlm.nih.gov/pubmed/33104690
http://dx.doi.org/10.1371/journal.pgen.1008800
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