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A foundational approach to culture and analyze malnourished organoids

The gastrointestinal (GI) epithelium plays a major role in nutrient absorption, barrier formation, and innate immunity. The development of organoid-based methodology has significantly impacted the study of the GI epithelium, particularly in the fields of mucosal biology, immunity, and host-microbe i...

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Autores principales: Perlman, Meryl, Senger, Stefania, Verma, Smriti, Carey, James, Faherty, Christina S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512930/
https://www.ncbi.nlm.nih.gov/pubmed/37724815
http://dx.doi.org/10.1080/19490976.2023.2248713
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author Perlman, Meryl
Senger, Stefania
Verma, Smriti
Carey, James
Faherty, Christina S.
author_facet Perlman, Meryl
Senger, Stefania
Verma, Smriti
Carey, James
Faherty, Christina S.
author_sort Perlman, Meryl
collection PubMed
description The gastrointestinal (GI) epithelium plays a major role in nutrient absorption, barrier formation, and innate immunity. The development of organoid-based methodology has significantly impacted the study of the GI epithelium, particularly in the fields of mucosal biology, immunity, and host-microbe interactions. Various effects on the GI epithelium, such as genetics and nutrition, impact patients and alter disease states. Thus, incorporating these effects into organoid-based models will facilitate a better understanding of disease progression and offer opportunities to evaluate therapeutic candidates. One condition that has a significant effect on the GI epithelium is malnutrition, and studying the mechanistic impacts of malnutrition would enhance our understanding of several pathologies. Therefore, the goal of this study was to begin to develop methodology to generate viable malnourished organoids with accessible techniques and resources that can be used for a wide array of mechanistic studies. By selectively limiting distinct macronutrient components of organoid media, we were able to successfully culture and evaluate malnourished organoids. Genetic and protein-based analyses were used to validate the approach and confirm the presence of known biomarkers of malnutrition. Additionally, as proof-of-concept, we utilized malnourished organoid-derived monolayers to evaluate the effect of malnourishment on barrier formation and the ability of the bacterial pathogen Shigella flexneri to infect the GI epithelium. This work serves as the basis for new and exciting techniques to alter the nutritional state of organoids and investigate the related impacts on the GI epithelium.
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spelling pubmed-105129302023-09-22 A foundational approach to culture and analyze malnourished organoids Perlman, Meryl Senger, Stefania Verma, Smriti Carey, James Faherty, Christina S. Gut Microbes Research Paper The gastrointestinal (GI) epithelium plays a major role in nutrient absorption, barrier formation, and innate immunity. The development of organoid-based methodology has significantly impacted the study of the GI epithelium, particularly in the fields of mucosal biology, immunity, and host-microbe interactions. Various effects on the GI epithelium, such as genetics and nutrition, impact patients and alter disease states. Thus, incorporating these effects into organoid-based models will facilitate a better understanding of disease progression and offer opportunities to evaluate therapeutic candidates. One condition that has a significant effect on the GI epithelium is malnutrition, and studying the mechanistic impacts of malnutrition would enhance our understanding of several pathologies. Therefore, the goal of this study was to begin to develop methodology to generate viable malnourished organoids with accessible techniques and resources that can be used for a wide array of mechanistic studies. By selectively limiting distinct macronutrient components of organoid media, we were able to successfully culture and evaluate malnourished organoids. Genetic and protein-based analyses were used to validate the approach and confirm the presence of known biomarkers of malnutrition. Additionally, as proof-of-concept, we utilized malnourished organoid-derived monolayers to evaluate the effect of malnourishment on barrier formation and the ability of the bacterial pathogen Shigella flexneri to infect the GI epithelium. This work serves as the basis for new and exciting techniques to alter the nutritional state of organoids and investigate the related impacts on the GI epithelium. Taylor & Francis 2023-09-19 /pmc/articles/PMC10512930/ /pubmed/37724815 http://dx.doi.org/10.1080/19490976.2023.2248713 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Paper
Perlman, Meryl
Senger, Stefania
Verma, Smriti
Carey, James
Faherty, Christina S.
A foundational approach to culture and analyze malnourished organoids
title A foundational approach to culture and analyze malnourished organoids
title_full A foundational approach to culture and analyze malnourished organoids
title_fullStr A foundational approach to culture and analyze malnourished organoids
title_full_unstemmed A foundational approach to culture and analyze malnourished organoids
title_short A foundational approach to culture and analyze malnourished organoids
title_sort foundational approach to culture and analyze malnourished organoids
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512930/
https://www.ncbi.nlm.nih.gov/pubmed/37724815
http://dx.doi.org/10.1080/19490976.2023.2248713
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