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Monitoring cell fate in 3D organotypic human squamous epithelial cultures

Here, we provide a protocol to model the effects of changes to a small number of cells, such as those arising from a mutation or a virus infection, in stratified epithelia. We describe steps for diluting engineered human keratinocytes into a larger population of unmodified cells and using these cell...

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Detalles Bibliográficos
Autores principales: Hatterschide, Joshua, Natale, Christopher A., Ridky, Todd W., White, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937944/
https://www.ncbi.nlm.nih.gov/pubmed/36853703
http://dx.doi.org/10.1016/j.xpro.2023.102101
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author Hatterschide, Joshua
Natale, Christopher A.
Ridky, Todd W.
White, Elizabeth A.
author_facet Hatterschide, Joshua
Natale, Christopher A.
Ridky, Todd W.
White, Elizabeth A.
author_sort Hatterschide, Joshua
collection PubMed
description Here, we provide a protocol to model the effects of changes to a small number of cells, such as those arising from a mutation or a virus infection, in stratified epithelia. We describe steps for diluting engineered human keratinocytes into a larger population of unmodified cells and using these cells to grow three-dimensional organotypic cultures. We detail steps to observe effects that are not apparent in homogenous organotypic epithelial cultures by visualizing the localization of modified keratinocytes in epithelial layers. For complete details on the use and execution of this protocol, please refer to Hatterschide et al. (2022).(1)
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spelling pubmed-99379442023-02-19 Monitoring cell fate in 3D organotypic human squamous epithelial cultures Hatterschide, Joshua Natale, Christopher A. Ridky, Todd W. White, Elizabeth A. STAR Protoc Protocol Here, we provide a protocol to model the effects of changes to a small number of cells, such as those arising from a mutation or a virus infection, in stratified epithelia. We describe steps for diluting engineered human keratinocytes into a larger population of unmodified cells and using these cells to grow three-dimensional organotypic cultures. We detail steps to observe effects that are not apparent in homogenous organotypic epithelial cultures by visualizing the localization of modified keratinocytes in epithelial layers. For complete details on the use and execution of this protocol, please refer to Hatterschide et al. (2022).(1) Elsevier 2023-02-06 /pmc/articles/PMC9937944/ /pubmed/36853703 http://dx.doi.org/10.1016/j.xpro.2023.102101 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Hatterschide, Joshua
Natale, Christopher A.
Ridky, Todd W.
White, Elizabeth A.
Monitoring cell fate in 3D organotypic human squamous epithelial cultures
title Monitoring cell fate in 3D organotypic human squamous epithelial cultures
title_full Monitoring cell fate in 3D organotypic human squamous epithelial cultures
title_fullStr Monitoring cell fate in 3D organotypic human squamous epithelial cultures
title_full_unstemmed Monitoring cell fate in 3D organotypic human squamous epithelial cultures
title_short Monitoring cell fate in 3D organotypic human squamous epithelial cultures
title_sort monitoring cell fate in 3d organotypic human squamous epithelial cultures
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937944/
https://www.ncbi.nlm.nih.gov/pubmed/36853703
http://dx.doi.org/10.1016/j.xpro.2023.102101
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