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3D sheep rumen epithelial structures driven from single cells in vitro

Ruminants play a vital economic role as livestock, providing high-quality protein for humans. At present, 3D-cultured ruminant abomasum and intestinal organoids have been successfully established to study host and pathogen interaction. The rumen is a unique digestive organ of ruminants that occupies...

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Autores principales: Xu, Zebang, Xu, Xinxin, Yang, Bin, Mi, Yuling, Wang, Jiakun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636852/
https://www.ncbi.nlm.nih.gov/pubmed/37946298
http://dx.doi.org/10.1186/s13567-023-01234-1
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author Xu, Zebang
Xu, Xinxin
Yang, Bin
Mi, Yuling
Wang, Jiakun
author_facet Xu, Zebang
Xu, Xinxin
Yang, Bin
Mi, Yuling
Wang, Jiakun
author_sort Xu, Zebang
collection PubMed
description Ruminants play a vital economic role as livestock, providing high-quality protein for humans. At present, 3D-cultured ruminant abomasum and intestinal organoids have been successfully established to study host and pathogen interaction. The rumen is a unique digestive organ of ruminants that occupies 70% of the volume of the digestive tract and its microbiota can decompose lignocellulose to support animal growth. Here we report a method for culturing rumen epithelial organoids. We found that single rumen epithelial cells form self-organized 3D structures representative of typical stratified squamous epithelium, which is similar to rumen epithelium. EGF, Noggin, Wnt3a, IGF-1, and FGF-10 significantly enhanced the seeding efficiency of organoids. Moreover, the inclusion of CHIR-99021, A83-01, SB202190, and Y-27632 is crucial for organoid formation and maintenance. Importantly, we demonstrate that rumen epithelial cells retain their ability to form organoids after passage, cryopreservation, and resuscitation. The rumen epithelial organoids express rumen cell type-specific genes, uptake fatty acids, and generate 2D cultures. In summary, our data demonstrate that it is feasible to establish organoids from single rumen epithelial cells, which is a novel in vitro system that may reduce the use of experimental animals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-023-01234-1.
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spelling pubmed-106368522023-11-11 3D sheep rumen epithelial structures driven from single cells in vitro Xu, Zebang Xu, Xinxin Yang, Bin Mi, Yuling Wang, Jiakun Vet Res Research Article Ruminants play a vital economic role as livestock, providing high-quality protein for humans. At present, 3D-cultured ruminant abomasum and intestinal organoids have been successfully established to study host and pathogen interaction. The rumen is a unique digestive organ of ruminants that occupies 70% of the volume of the digestive tract and its microbiota can decompose lignocellulose to support animal growth. Here we report a method for culturing rumen epithelial organoids. We found that single rumen epithelial cells form self-organized 3D structures representative of typical stratified squamous epithelium, which is similar to rumen epithelium. EGF, Noggin, Wnt3a, IGF-1, and FGF-10 significantly enhanced the seeding efficiency of organoids. Moreover, the inclusion of CHIR-99021, A83-01, SB202190, and Y-27632 is crucial for organoid formation and maintenance. Importantly, we demonstrate that rumen epithelial cells retain their ability to form organoids after passage, cryopreservation, and resuscitation. The rumen epithelial organoids express rumen cell type-specific genes, uptake fatty acids, and generate 2D cultures. In summary, our data demonstrate that it is feasible to establish organoids from single rumen epithelial cells, which is a novel in vitro system that may reduce the use of experimental animals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-023-01234-1. BioMed Central 2023-11-09 2023 /pmc/articles/PMC10636852/ /pubmed/37946298 http://dx.doi.org/10.1186/s13567-023-01234-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/ Open Access This 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 Research Article
Xu, Zebang
Xu, Xinxin
Yang, Bin
Mi, Yuling
Wang, Jiakun
3D sheep rumen epithelial structures driven from single cells in vitro
title 3D sheep rumen epithelial structures driven from single cells in vitro
title_full 3D sheep rumen epithelial structures driven from single cells in vitro
title_fullStr 3D sheep rumen epithelial structures driven from single cells in vitro
title_full_unstemmed 3D sheep rumen epithelial structures driven from single cells in vitro
title_short 3D sheep rumen epithelial structures driven from single cells in vitro
title_sort 3d sheep rumen epithelial structures driven from single cells in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636852/
https://www.ncbi.nlm.nih.gov/pubmed/37946298
http://dx.doi.org/10.1186/s13567-023-01234-1
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