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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...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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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. |
format | Text |
id | pubmed-2803788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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