Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783398361930399744 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6391775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT cojuliay controllingepithelialpolarityahumanenteroidmodelforhostpathogeninteractions AT margalefcatalamar controllingepithelialpolarityahumanenteroidmodelforhostpathogeninteractions AT lixingnan controllingepithelialpolarityahumanenteroidmodelforhostpathogeninteractions AT mahamandat controllingepithelialpolarityahumanenteroidmodelforhostpathogeninteractions AT kuocalvinj controllingepithelialpolarityahumanenteroidmodelforhostpathogeninteractions AT monackdenisem controllingepithelialpolarityahumanenteroidmodelforhostpathogeninteractions AT amievamanuelr controllingepithelialpolarityahumanenteroidmodelforhostpathogeninteractions |