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Generation of BAC Transgenic Epithelial Organoids

Under previously developed culture conditions, mouse and human intestinal epithelia can be cultured and expanded over long periods. These so-called organoids recapitulate the three-dimensional architecture of the gut epithelium, and consist of all major intestinal cell types. One key advantage of th...

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Detalles Bibliográficos
Autores principales: Schwank, Gerald, Andersson-Rolf, Amanda, Koo, Bon-Kyoung, Sasaki, Nobuo, Clevers, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800075/
https://www.ncbi.nlm.nih.gov/pubmed/24204693
http://dx.doi.org/10.1371/journal.pone.0076871
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author Schwank, Gerald
Andersson-Rolf, Amanda
Koo, Bon-Kyoung
Sasaki, Nobuo
Clevers, Hans
author_facet Schwank, Gerald
Andersson-Rolf, Amanda
Koo, Bon-Kyoung
Sasaki, Nobuo
Clevers, Hans
author_sort Schwank, Gerald
collection PubMed
description Under previously developed culture conditions, mouse and human intestinal epithelia can be cultured and expanded over long periods. These so-called organoids recapitulate the three-dimensional architecture of the gut epithelium, and consist of all major intestinal cell types. One key advantage of these ex vivo cultures is their accessibility to live imaging. So far the establishment of transgenic fluorescent reporter organoids has required the generation of transgenic mice, a laborious and time-consuming process, which cannot be extended to human cultures. Here we present a transfection protocol that enables the generation of recombinant mouse and human reporter organoids using BAC (bacterial artificial chromosome) technology.
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spelling pubmed-38000752013-11-07 Generation of BAC Transgenic Epithelial Organoids Schwank, Gerald Andersson-Rolf, Amanda Koo, Bon-Kyoung Sasaki, Nobuo Clevers, Hans PLoS One Research Article Under previously developed culture conditions, mouse and human intestinal epithelia can be cultured and expanded over long periods. These so-called organoids recapitulate the three-dimensional architecture of the gut epithelium, and consist of all major intestinal cell types. One key advantage of these ex vivo cultures is their accessibility to live imaging. So far the establishment of transgenic fluorescent reporter organoids has required the generation of transgenic mice, a laborious and time-consuming process, which cannot be extended to human cultures. Here we present a transfection protocol that enables the generation of recombinant mouse and human reporter organoids using BAC (bacterial artificial chromosome) technology. Public Library of Science 2013-10-18 /pmc/articles/PMC3800075/ /pubmed/24204693 http://dx.doi.org/10.1371/journal.pone.0076871 Text en © 2013 Schwank et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schwank, Gerald
Andersson-Rolf, Amanda
Koo, Bon-Kyoung
Sasaki, Nobuo
Clevers, Hans
Generation of BAC Transgenic Epithelial Organoids
title Generation of BAC Transgenic Epithelial Organoids
title_full Generation of BAC Transgenic Epithelial Organoids
title_fullStr Generation of BAC Transgenic Epithelial Organoids
title_full_unstemmed Generation of BAC Transgenic Epithelial Organoids
title_short Generation of BAC Transgenic Epithelial Organoids
title_sort generation of bac transgenic epithelial organoids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800075/
https://www.ncbi.nlm.nih.gov/pubmed/24204693
http://dx.doi.org/10.1371/journal.pone.0076871
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