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Isolation and feeder-free primary culture of four cell types from a single human skin sample

Four types of primary cells—dermal fibroblasts, dermal microvascular endothelial cells, epidermal keratinocytes, and epidermal melanocytes—can be isolated simultaneously from a single human skin sample, without the use of xenogeneic murine feeder cells. This protocol describes the procedures for iso...

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Detalles Bibliográficos
Autores principales: Supp, Dorothy M., Hahn, Jennifer M., Combs, Kelly A., McFarland, Kevin L., Powell, Heather M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844903/
https://www.ncbi.nlm.nih.gov/pubmed/35199036
http://dx.doi.org/10.1016/j.xpro.2022.101172
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author Supp, Dorothy M.
Hahn, Jennifer M.
Combs, Kelly A.
McFarland, Kevin L.
Powell, Heather M.
author_facet Supp, Dorothy M.
Hahn, Jennifer M.
Combs, Kelly A.
McFarland, Kevin L.
Powell, Heather M.
author_sort Supp, Dorothy M.
collection PubMed
description Four types of primary cells—dermal fibroblasts, dermal microvascular endothelial cells, epidermal keratinocytes, and epidermal melanocytes—can be isolated simultaneously from a single human skin sample, without the use of xenogeneic murine feeder cells. This protocol describes the procedures for isolation of these cells from adult full-thickness skin obtained from surgical discard tissue. The cells isolated using this protocol contain stem cell populations and are competent to form functional skin tissue in three-dimensional reconstructed skin models. For complete details on the use and execution of this profile, please refer to Supp et al. (2002), Boyce et al. (2015), Boyce et al. (2017a), Boyce et al. (2017b), and Supp et al. (2019).
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spelling pubmed-88449032022-02-22 Isolation and feeder-free primary culture of four cell types from a single human skin sample Supp, Dorothy M. Hahn, Jennifer M. Combs, Kelly A. McFarland, Kevin L. Powell, Heather M. STAR Protoc Protocol Four types of primary cells—dermal fibroblasts, dermal microvascular endothelial cells, epidermal keratinocytes, and epidermal melanocytes—can be isolated simultaneously from a single human skin sample, without the use of xenogeneic murine feeder cells. This protocol describes the procedures for isolation of these cells from adult full-thickness skin obtained from surgical discard tissue. The cells isolated using this protocol contain stem cell populations and are competent to form functional skin tissue in three-dimensional reconstructed skin models. For complete details on the use and execution of this profile, please refer to Supp et al. (2002), Boyce et al. (2015), Boyce et al. (2017a), Boyce et al. (2017b), and Supp et al. (2019). Elsevier 2022-02-10 /pmc/articles/PMC8844903/ /pubmed/35199036 http://dx.doi.org/10.1016/j.xpro.2022.101172 Text en © 2022 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
Supp, Dorothy M.
Hahn, Jennifer M.
Combs, Kelly A.
McFarland, Kevin L.
Powell, Heather M.
Isolation and feeder-free primary culture of four cell types from a single human skin sample
title Isolation and feeder-free primary culture of four cell types from a single human skin sample
title_full Isolation and feeder-free primary culture of four cell types from a single human skin sample
title_fullStr Isolation and feeder-free primary culture of four cell types from a single human skin sample
title_full_unstemmed Isolation and feeder-free primary culture of four cell types from a single human skin sample
title_short Isolation and feeder-free primary culture of four cell types from a single human skin sample
title_sort isolation and feeder-free primary culture of four cell types from a single human skin sample
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844903/
https://www.ncbi.nlm.nih.gov/pubmed/35199036
http://dx.doi.org/10.1016/j.xpro.2022.101172
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