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Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium

Endothelial cells (ECs), which line blood and lymphatic vessels, are generally described to come from the lateral plate mesoderm despite experimental evidence for a broader source of origin, including the paraxial mesoderm (PXM). Current dogma suggests that following specification from mesoderm, loc...

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Detalles Bibliográficos
Autores principales: Stone, Oliver A., Stainier, Didier Y.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658618/
https://www.ncbi.nlm.nih.gov/pubmed/31130354
http://dx.doi.org/10.1016/j.devcel.2019.04.034
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author Stone, Oliver A.
Stainier, Didier Y.R.
author_facet Stone, Oliver A.
Stainier, Didier Y.R.
author_sort Stone, Oliver A.
collection PubMed
description Endothelial cells (ECs), which line blood and lymphatic vessels, are generally described to come from the lateral plate mesoderm despite experimental evidence for a broader source of origin, including the paraxial mesoderm (PXM). Current dogma suggests that following specification from mesoderm, local environmental cues establish the distinct molecular and functional characteristics of ECs in different vascular beds. Here we present evidence to challenge this view, showing that lymphatic EC fate is imprinted during transition through the PXM lineage. We show that PXM-derived cells form the lymphatic endothelium of multiple organs and tissues, with a more restricted contribution to blood vessel endothelium. By deleting Prox1 specifically in PXM-derived cells, we show that this lineage is indispensable for lymphatic vessel development. Collectively, our data establish lineage history as a critical determinant of EC specialization, a finding with broad implications for our understanding of vascular development and heterogeneity.
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spelling pubmed-66586182019-08-06 Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium Stone, Oliver A. Stainier, Didier Y.R. Dev Cell Article Endothelial cells (ECs), which line blood and lymphatic vessels, are generally described to come from the lateral plate mesoderm despite experimental evidence for a broader source of origin, including the paraxial mesoderm (PXM). Current dogma suggests that following specification from mesoderm, local environmental cues establish the distinct molecular and functional characteristics of ECs in different vascular beds. Here we present evidence to challenge this view, showing that lymphatic EC fate is imprinted during transition through the PXM lineage. We show that PXM-derived cells form the lymphatic endothelium of multiple organs and tissues, with a more restricted contribution to blood vessel endothelium. By deleting Prox1 specifically in PXM-derived cells, we show that this lineage is indispensable for lymphatic vessel development. Collectively, our data establish lineage history as a critical determinant of EC specialization, a finding with broad implications for our understanding of vascular development and heterogeneity. Cell Press 2019-07-22 /pmc/articles/PMC6658618/ /pubmed/31130354 http://dx.doi.org/10.1016/j.devcel.2019.04.034 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Stone, Oliver A.
Stainier, Didier Y.R.
Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium
title Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium
title_full Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium
title_fullStr Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium
title_full_unstemmed Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium
title_short Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium
title_sort paraxial mesoderm is the major source of lymphatic endothelium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658618/
https://www.ncbi.nlm.nih.gov/pubmed/31130354
http://dx.doi.org/10.1016/j.devcel.2019.04.034
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