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Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions

Human enteroids—epithelial spheroids derived from primary gastrointestinal tissue—are a promising model to study pathogen-epithelial interactions. However, accessing the apical enteroid surface is challenging because it is enclosed within the spheroid. We developed a technique to reverse enteroid po...

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Detalles Bibliográficos
Autores principales: Co, Julia Y., Margalef-Català, Mar, Li, Xingnan, Mah, Amanda T., Kuo, Calvin J., Monack, Denise M., Amieva, Manuel R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391775/
https://www.ncbi.nlm.nih.gov/pubmed/30811997
http://dx.doi.org/10.1016/j.celrep.2019.01.108
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author Co, Julia Y.
Margalef-Català, Mar
Li, Xingnan
Mah, Amanda T.
Kuo, Calvin J.
Monack, Denise M.
Amieva, Manuel R.
author_facet Co, Julia Y.
Margalef-Català, Mar
Li, Xingnan
Mah, Amanda T.
Kuo, Calvin J.
Monack, Denise M.
Amieva, Manuel R.
author_sort Co, Julia Y.
collection PubMed
description Human enteroids—epithelial spheroids derived from primary gastrointestinal tissue—are a promising model to study pathogen-epithelial interactions. However, accessing the apical enteroid surface is challenging because it is enclosed within the spheroid. We developed a technique to reverse enteroid polarity such that the apical surface everts to face the media. Apical-out enteroids maintain proper polarity and barrier function, differentiate into the major intestinal epithelial cell (IEC) types, and exhibit polarized absorption of nutrients. We used this model to study host-pathogen interactions and identified distinct polarity-specific patterns of infection by invasive enteropathogens. Salmonella enterica serovar Typhimurium targets IEC apical surfaces for invasion via cytoskeletal rearrangements, and Listeria monocytogenes, which binds to basolateral receptors, invade apical surfaces at sites of cell extrusion. Despite different modes of entry, both pathogens exit the epithelium within apically extruding enteroid cells. This model will enable further examination of IECs in health and disease.
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spelling pubmed-63917752019-03-07 Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions Co, Julia Y. Margalef-Català, Mar Li, Xingnan Mah, Amanda T. Kuo, Calvin J. Monack, Denise M. Amieva, Manuel R. Cell Rep Article Human enteroids—epithelial spheroids derived from primary gastrointestinal tissue—are a promising model to study pathogen-epithelial interactions. However, accessing the apical enteroid surface is challenging because it is enclosed within the spheroid. We developed a technique to reverse enteroid polarity such that the apical surface everts to face the media. Apical-out enteroids maintain proper polarity and barrier function, differentiate into the major intestinal epithelial cell (IEC) types, and exhibit polarized absorption of nutrients. We used this model to study host-pathogen interactions and identified distinct polarity-specific patterns of infection by invasive enteropathogens. Salmonella enterica serovar Typhimurium targets IEC apical surfaces for invasion via cytoskeletal rearrangements, and Listeria monocytogenes, which binds to basolateral receptors, invade apical surfaces at sites of cell extrusion. Despite different modes of entry, both pathogens exit the epithelium within apically extruding enteroid cells. This model will enable further examination of IECs in health and disease. Cell Press 2019-02-26 /pmc/articles/PMC6391775/ /pubmed/30811997 http://dx.doi.org/10.1016/j.celrep.2019.01.108 Text en © 2019 The Author(s) http://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 Article
Co, Julia Y.
Margalef-Català, Mar
Li, Xingnan
Mah, Amanda T.
Kuo, Calvin J.
Monack, Denise M.
Amieva, Manuel R.
Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions
title Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions
title_full Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions
title_fullStr Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions
title_full_unstemmed Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions
title_short Controlling Epithelial Polarity: A Human Enteroid Model for Host-Pathogen Interactions
title_sort controlling epithelial polarity: a human enteroid model for host-pathogen interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391775/
https://www.ncbi.nlm.nih.gov/pubmed/30811997
http://dx.doi.org/10.1016/j.celrep.2019.01.108
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