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Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium
A single layer of squamous endothelial cells (ECs), the endothelium, regulates the flow of substance and fluid into and out of a tissue. The endothelium is also involved in vasculogenesis, the formation of new blood vessels, which is a crucial process for organ development in the embryo and fetus. B...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society of Lipidology and Atherosclerosis
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838514/ https://www.ncbi.nlm.nih.gov/pubmed/33537251 http://dx.doi.org/10.12997/jla.2021.10.1.24 |
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author | Lee, Ho |
author_facet | Lee, Ho |
author_sort | Lee, Ho |
collection | PubMed |
description | A single layer of squamous endothelial cells (ECs), the endothelium, regulates the flow of substance and fluid into and out of a tissue. The endothelium is also involved in vasculogenesis, the formation of new blood vessels, which is a crucial process for organ development in the embryo and fetus. Because most murine mutations of genes involved in EC development cause early embryo lethality, EC-specific conditional knockout (cKO) mouse models are indispensable for in vivo studies. cKO mice including the floxed allele can be generated through advanced approaches including embryonic stem cell-mediated gene targeting or the CRISPR/Cas system. EC-specific mouse models can be generated through further breeding of floxed mice with a Cre driver line, the latest information of which is available in the Jackson Cre Repository or the EUCOMMTOOLS project. Because it takes a long time (generally 1–2 years) to generate EC-specific mouse models, researchers must thoroughly design and plan a breeding strategy before full-scale mouse experiments, which saves time and money for in vivo study. In summary, revolutionary technical advances in embryo manipulation and assisted reproduction technologies have made it easier to generate EC-specific mouse models, which have been used as essential resources for in vivo studies of the endothelium. |
format | Online Article Text |
id | pubmed-7838514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean Society of Lipidology and Atherosclerosis |
record_format | MEDLINE/PubMed |
spelling | pubmed-78385142021-02-02 Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium Lee, Ho J Lipid Atheroscler Review A single layer of squamous endothelial cells (ECs), the endothelium, regulates the flow of substance and fluid into and out of a tissue. The endothelium is also involved in vasculogenesis, the formation of new blood vessels, which is a crucial process for organ development in the embryo and fetus. Because most murine mutations of genes involved in EC development cause early embryo lethality, EC-specific conditional knockout (cKO) mouse models are indispensable for in vivo studies. cKO mice including the floxed allele can be generated through advanced approaches including embryonic stem cell-mediated gene targeting or the CRISPR/Cas system. EC-specific mouse models can be generated through further breeding of floxed mice with a Cre driver line, the latest information of which is available in the Jackson Cre Repository or the EUCOMMTOOLS project. Because it takes a long time (generally 1–2 years) to generate EC-specific mouse models, researchers must thoroughly design and plan a breeding strategy before full-scale mouse experiments, which saves time and money for in vivo study. In summary, revolutionary technical advances in embryo manipulation and assisted reproduction technologies have made it easier to generate EC-specific mouse models, which have been used as essential resources for in vivo studies of the endothelium. Korean Society of Lipidology and Atherosclerosis 2021-01 2020-11-17 /pmc/articles/PMC7838514/ /pubmed/33537251 http://dx.doi.org/10.12997/jla.2021.10.1.24 Text en Copyright © 2021 The Korean Society of Lipid and Atherosclerosis. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Lee, Ho Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium |
title | Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium |
title_full | Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium |
title_fullStr | Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium |
title_full_unstemmed | Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium |
title_short | Rapid Way to Generate Mouse Models for In Vivo Studies of the Endothelium |
title_sort | rapid way to generate mouse models for in vivo studies of the endothelium |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838514/ https://www.ncbi.nlm.nih.gov/pubmed/33537251 http://dx.doi.org/10.12997/jla.2021.10.1.24 |
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