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ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming
Extensive efforts have been made to achieve vascular regeneration accompanying tissue repair for treating vascular dysfunction-associated diseases. Recent advancements in stem cell biology and cell reprogramming have opened unforeseen opportunities to promote angiogenesis in vivo and generate autolo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019431/ https://www.ncbi.nlm.nih.gov/pubmed/36927793 http://dx.doi.org/10.1186/s13287-023-03267-x |
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author | Kim, Tae Min Lee, Ra Ham Kim, Min Seong Lewis, Chloe A. Park, Changwon |
author_facet | Kim, Tae Min Lee, Ra Ham Kim, Min Seong Lewis, Chloe A. Park, Changwon |
author_sort | Kim, Tae Min |
collection | PubMed |
description | Extensive efforts have been made to achieve vascular regeneration accompanying tissue repair for treating vascular dysfunction-associated diseases. Recent advancements in stem cell biology and cell reprogramming have opened unforeseen opportunities to promote angiogenesis in vivo and generate autologous endothelial cells (ECs) for clinical use. We have, for the first time, identified a unique endothelial-specific transcription factor, ETV2/ER71, and revealed its essential role in regulating endothelial cell generation and function, along with vascular regeneration and tissue repair. Furthermore, we and other groups have demonstrated its ability to directly reprogram terminally differentiated non-ECs into functional ECs, proposing ETV2/ER71 as an effective therapeutic target for vascular diseases. In this review, we discuss the up-to-date status of studies on ETV2/ER71, spanning from its molecular mechanism to vasculo-angiogenic role and direct cell reprogramming toward ECs. Furthermore, we discuss future directions to deploy the clinical potential of ETV2/ER71 as a novel and potent target for vascular disorders such as cardiovascular disease, neurovascular impairment and cancer. |
format | Online Article Text |
id | pubmed-10019431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100194312023-03-16 ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming Kim, Tae Min Lee, Ra Ham Kim, Min Seong Lewis, Chloe A. Park, Changwon Stem Cell Res Ther Review Extensive efforts have been made to achieve vascular regeneration accompanying tissue repair for treating vascular dysfunction-associated diseases. Recent advancements in stem cell biology and cell reprogramming have opened unforeseen opportunities to promote angiogenesis in vivo and generate autologous endothelial cells (ECs) for clinical use. We have, for the first time, identified a unique endothelial-specific transcription factor, ETV2/ER71, and revealed its essential role in regulating endothelial cell generation and function, along with vascular regeneration and tissue repair. Furthermore, we and other groups have demonstrated its ability to directly reprogram terminally differentiated non-ECs into functional ECs, proposing ETV2/ER71 as an effective therapeutic target for vascular diseases. In this review, we discuss the up-to-date status of studies on ETV2/ER71, spanning from its molecular mechanism to vasculo-angiogenic role and direct cell reprogramming toward ECs. Furthermore, we discuss future directions to deploy the clinical potential of ETV2/ER71 as a novel and potent target for vascular disorders such as cardiovascular disease, neurovascular impairment and cancer. BioMed Central 2023-03-16 /pmc/articles/PMC10019431/ /pubmed/36927793 http://dx.doi.org/10.1186/s13287-023-03267-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Kim, Tae Min Lee, Ra Ham Kim, Min Seong Lewis, Chloe A. Park, Changwon ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming |
title | ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming |
title_full | ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming |
title_fullStr | ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming |
title_full_unstemmed | ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming |
title_short | ETV2/ER71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming |
title_sort | etv2/er71, the key factor leading the paths to vascular regeneration and angiogenic reprogramming |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019431/ https://www.ncbi.nlm.nih.gov/pubmed/36927793 http://dx.doi.org/10.1186/s13287-023-03267-x |
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