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Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells
Vascular endothelium is a dynamic cellular interface that displays a unique phenotypic plasticity. This plasticity is critical for vascular function and when dysregulated is pathogenic in several diseases. Human genotype-phenotype studies of endothelium are limited by the unavailability of patient-s...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757754/ https://www.ncbi.nlm.nih.gov/pubmed/24052946 http://dx.doi.org/10.1016/j.stemcr.2013.06.007 |
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author | Adams, William J. Zhang, Yuzhi Cloutier, Jennifer Kuchimanchi, Pranati Newton, Gail Sehrawat, Seema Aird, William C. Mayadas, Tanya N. Luscinskas, Francis W. García-Cardeña, Guillermo |
author_facet | Adams, William J. Zhang, Yuzhi Cloutier, Jennifer Kuchimanchi, Pranati Newton, Gail Sehrawat, Seema Aird, William C. Mayadas, Tanya N. Luscinskas, Francis W. García-Cardeña, Guillermo |
author_sort | Adams, William J. |
collection | PubMed |
description | Vascular endothelium is a dynamic cellular interface that displays a unique phenotypic plasticity. This plasticity is critical for vascular function and when dysregulated is pathogenic in several diseases. Human genotype-phenotype studies of endothelium are limited by the unavailability of patient-specific endothelial cells. To establish a cellular platform for studying endothelial biology, we have generated vascular endothelium from human induced pluripotent stem cells (iPSCs) exhibiting the rich functional phenotypic plasticity of mature primary vascular endothelium. These endothelial cells respond to diverse proinflammatory stimuli, adopting an activated phenotype including leukocyte adhesion molecule expression, cytokine production, and support for leukocyte transmigration. They maintain dynamic barrier properties responsive to multiple vascular permeability factors. Importantly, biomechanical or pharmacological stimuli can induce pathophysiologically relevant atheroprotective or atheroprone phenotypes. Our results demonstrate that iPSC-derived endothelium possesses a repertoire of functional phenotypic plasticity and is amenable to cell-based assays probing endothelial contributions to inflammatory and cardiovascular diseases. |
format | Online Article Text |
id | pubmed-3757754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-37577542013-09-17 Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells Adams, William J. Zhang, Yuzhi Cloutier, Jennifer Kuchimanchi, Pranati Newton, Gail Sehrawat, Seema Aird, William C. Mayadas, Tanya N. Luscinskas, Francis W. García-Cardeña, Guillermo Stem Cell Reports Report Vascular endothelium is a dynamic cellular interface that displays a unique phenotypic plasticity. This plasticity is critical for vascular function and when dysregulated is pathogenic in several diseases. Human genotype-phenotype studies of endothelium are limited by the unavailability of patient-specific endothelial cells. To establish a cellular platform for studying endothelial biology, we have generated vascular endothelium from human induced pluripotent stem cells (iPSCs) exhibiting the rich functional phenotypic plasticity of mature primary vascular endothelium. These endothelial cells respond to diverse proinflammatory stimuli, adopting an activated phenotype including leukocyte adhesion molecule expression, cytokine production, and support for leukocyte transmigration. They maintain dynamic barrier properties responsive to multiple vascular permeability factors. Importantly, biomechanical or pharmacological stimuli can induce pathophysiologically relevant atheroprotective or atheroprone phenotypes. Our results demonstrate that iPSC-derived endothelium possesses a repertoire of functional phenotypic plasticity and is amenable to cell-based assays probing endothelial contributions to inflammatory and cardiovascular diseases. Elsevier 2013-07-25 /pmc/articles/PMC3757754/ /pubmed/24052946 http://dx.doi.org/10.1016/j.stemcr.2013.06.007 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Report Adams, William J. Zhang, Yuzhi Cloutier, Jennifer Kuchimanchi, Pranati Newton, Gail Sehrawat, Seema Aird, William C. Mayadas, Tanya N. Luscinskas, Francis W. García-Cardeña, Guillermo Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells |
title | Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells |
title_full | Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells |
title_fullStr | Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells |
title_full_unstemmed | Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells |
title_short | Functional Vascular Endothelium Derived from Human Induced Pluripotent Stem Cells |
title_sort | functional vascular endothelium derived from human induced pluripotent stem cells |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757754/ https://www.ncbi.nlm.nih.gov/pubmed/24052946 http://dx.doi.org/10.1016/j.stemcr.2013.06.007 |
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