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Generation, culture, and stimulation of small intestinal murine organoids in parasitology research

Parasitic helminth worms frequently infect the gastrointestinal tract and interact with the intestinal epithelium and specialized cell types within it. Intestinal organoids derived from stem cells that line the intestine represent a transformational technology in the study of epithelial-parasite dia...

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Autores principales: Campillo Poveda, Marta, Drurey, Claire, Maizels, Rick M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520931/
https://www.ncbi.nlm.nih.gov/pubmed/37751353
http://dx.doi.org/10.1016/j.xpro.2023.102608
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author Campillo Poveda, Marta
Drurey, Claire
Maizels, Rick M.
author_facet Campillo Poveda, Marta
Drurey, Claire
Maizels, Rick M.
author_sort Campillo Poveda, Marta
collection PubMed
description Parasitic helminth worms frequently infect the gastrointestinal tract and interact with the intestinal epithelium and specialized cell types within it. Intestinal organoids derived from stem cells that line the intestine represent a transformational technology in the study of epithelial-parasite dialogue. Here, we present a protocol for establishing small intestine organoid cultures and administering parasite products of interest to these cultures. We then describe steps for evaluating their impact by microscopy, flow cytometry, immunohistology, and mRNA gene expression. For complete details on the use and execution of this protocol, please refer to Drurey et al. (2022).(1)
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spelling pubmed-105209312023-09-27 Generation, culture, and stimulation of small intestinal murine organoids in parasitology research Campillo Poveda, Marta Drurey, Claire Maizels, Rick M. STAR Protoc Protocol Parasitic helminth worms frequently infect the gastrointestinal tract and interact with the intestinal epithelium and specialized cell types within it. Intestinal organoids derived from stem cells that line the intestine represent a transformational technology in the study of epithelial-parasite dialogue. Here, we present a protocol for establishing small intestine organoid cultures and administering parasite products of interest to these cultures. We then describe steps for evaluating their impact by microscopy, flow cytometry, immunohistology, and mRNA gene expression. For complete details on the use and execution of this protocol, please refer to Drurey et al. (2022).(1) Elsevier 2023-09-25 /pmc/articles/PMC10520931/ /pubmed/37751353 http://dx.doi.org/10.1016/j.xpro.2023.102608 Text en Crown Copyright © 2023. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Campillo Poveda, Marta
Drurey, Claire
Maizels, Rick M.
Generation, culture, and stimulation of small intestinal murine organoids in parasitology research
title Generation, culture, and stimulation of small intestinal murine organoids in parasitology research
title_full Generation, culture, and stimulation of small intestinal murine organoids in parasitology research
title_fullStr Generation, culture, and stimulation of small intestinal murine organoids in parasitology research
title_full_unstemmed Generation, culture, and stimulation of small intestinal murine organoids in parasitology research
title_short Generation, culture, and stimulation of small intestinal murine organoids in parasitology research
title_sort generation, culture, and stimulation of small intestinal murine organoids in parasitology research
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520931/
https://www.ncbi.nlm.nih.gov/pubmed/37751353
http://dx.doi.org/10.1016/j.xpro.2023.102608
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