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ERG is required for the differentiation of embryonic stem cells along the endothelial lineage

BACKGROUND: The molecular mechanisms that govern stem cell differentiation along the endothelial lineage remain largely unknown. Ets related gene (ERG) has recently been shown to participate in the transcriptional regulation of a number of endothelial specific genes including VE-cadherin (CD144), en...

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Autores principales: Nikolova-Krstevski, Vesna, Yuan, Lei, Le Bras, Alexandra, Vijayaraj, Preethi, Kondo, Maiko, Gebauer, Isabel, Bhasin, Manoj, Carman, Chris V, Oettgen, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2803788/
https://www.ncbi.nlm.nih.gov/pubmed/20030844
http://dx.doi.org/10.1186/1471-213X-9-72
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author Nikolova-Krstevski, Vesna
Yuan, Lei
Le Bras, Alexandra
Vijayaraj, Preethi
Kondo, Maiko
Gebauer, Isabel
Bhasin, Manoj
Carman, Chris V
Oettgen, Peter
author_facet Nikolova-Krstevski, Vesna
Yuan, Lei
Le Bras, Alexandra
Vijayaraj, Preethi
Kondo, Maiko
Gebauer, Isabel
Bhasin, Manoj
Carman, Chris V
Oettgen, Peter
author_sort Nikolova-Krstevski, Vesna
collection PubMed
description BACKGROUND: The molecular mechanisms that govern stem cell differentiation along the endothelial lineage remain largely unknown. Ets related gene (ERG) has recently been shown to participate in the transcriptional regulation of a number of endothelial specific genes including VE-cadherin (CD144), endoglin, and von Willebrand's Factor (vWF). The specific role of the ETS factor ERG during endothelial differentiation has not been evaluated. RESULTS: ERG expression and function were evaluated during the differentiation of embryonic stem cells into embryoid bodies (EB). The results of our study demonstrate that ERG is first expressed in a subpopulation of vascular endothelial growth factor receptor 2 (VEGF-R2) expressing cells that also express VE-cadherin. During ES cell differentiation, ERG expression remains restricted to cells of the endothelial lineage that eventually coalesce into primitive vascular structures within embryoid bodies. ERG also exhibits an endothelial cell (EC)-restricted pattern during embryogenesis. To further define the role of ERG during ES cell differentiation, we used a knockdown strategy to inhibit ERG expression. Delivery of three independent shRNA led to 70-85% reductions in ERG expression during ES cell differentiation compared to no change with control shRNA. ERG knockdown was associated with a marked reduction in the number of ECs, the expression of EC-restricted genes, and the formation of vascular structures. CONCLUSION: The ETS factor ERG appears to be a critical regulator of EC differentiation.
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spelling pubmed-28037882010-01-10 ERG is required for the differentiation of embryonic stem cells along the endothelial lineage Nikolova-Krstevski, Vesna Yuan, Lei Le Bras, Alexandra Vijayaraj, Preethi Kondo, Maiko Gebauer, Isabel Bhasin, Manoj Carman, Chris V Oettgen, Peter BMC Dev Biol Research article BACKGROUND: The molecular mechanisms that govern stem cell differentiation along the endothelial lineage remain largely unknown. Ets related gene (ERG) has recently been shown to participate in the transcriptional regulation of a number of endothelial specific genes including VE-cadherin (CD144), endoglin, and von Willebrand's Factor (vWF). The specific role of the ETS factor ERG during endothelial differentiation has not been evaluated. RESULTS: ERG expression and function were evaluated during the differentiation of embryonic stem cells into embryoid bodies (EB). The results of our study demonstrate that ERG is first expressed in a subpopulation of vascular endothelial growth factor receptor 2 (VEGF-R2) expressing cells that also express VE-cadherin. During ES cell differentiation, ERG expression remains restricted to cells of the endothelial lineage that eventually coalesce into primitive vascular structures within embryoid bodies. ERG also exhibits an endothelial cell (EC)-restricted pattern during embryogenesis. To further define the role of ERG during ES cell differentiation, we used a knockdown strategy to inhibit ERG expression. Delivery of three independent shRNA led to 70-85% reductions in ERG expression during ES cell differentiation compared to no change with control shRNA. ERG knockdown was associated with a marked reduction in the number of ECs, the expression of EC-restricted genes, and the formation of vascular structures. CONCLUSION: The ETS factor ERG appears to be a critical regulator of EC differentiation. BioMed Central 2009-12-23 /pmc/articles/PMC2803788/ /pubmed/20030844 http://dx.doi.org/10.1186/1471-213X-9-72 Text en Copyright ©2009 Nikolova-Krstevski et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Nikolova-Krstevski, Vesna
Yuan, Lei
Le Bras, Alexandra
Vijayaraj, Preethi
Kondo, Maiko
Gebauer, Isabel
Bhasin, Manoj
Carman, Chris V
Oettgen, Peter
ERG is required for the differentiation of embryonic stem cells along the endothelial lineage
title ERG is required for the differentiation of embryonic stem cells along the endothelial lineage
title_full ERG is required for the differentiation of embryonic stem cells along the endothelial lineage
title_fullStr ERG is required for the differentiation of embryonic stem cells along the endothelial lineage
title_full_unstemmed ERG is required for the differentiation of embryonic stem cells along the endothelial lineage
title_short ERG is required for the differentiation of embryonic stem cells along the endothelial lineage
title_sort erg is required for the differentiation of embryonic stem cells along the endothelial lineage
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2803788/
https://www.ncbi.nlm.nih.gov/pubmed/20030844
http://dx.doi.org/10.1186/1471-213X-9-72
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