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Isolation of five different primary cell types from a single sample of human skin

We have developed a technique to isolate primary keratinocytes, melanocytes, fibroblasts, preadipocytes, and microvascular endothelial cells from an individual sample of human skin. The protocol describes step-by-step instructions for processing, cells isolation, and culture of neonatal foreskin, wi...

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Detalles Bibliográficos
Autores principales: Kabacik, Sylwia, Lowe, Donna, Cohen, Howard, Felton, Sarah, Spitzer, Joseph, Raj, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108981/
https://www.ncbi.nlm.nih.gov/pubmed/35586317
http://dx.doi.org/10.1016/j.xpro.2022.101378
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author Kabacik, Sylwia
Lowe, Donna
Cohen, Howard
Felton, Sarah
Spitzer, Joseph
Raj, Ken
author_facet Kabacik, Sylwia
Lowe, Donna
Cohen, Howard
Felton, Sarah
Spitzer, Joseph
Raj, Ken
author_sort Kabacik, Sylwia
collection PubMed
description We have developed a technique to isolate primary keratinocytes, melanocytes, fibroblasts, preadipocytes, and microvascular endothelial cells from an individual sample of human skin. The protocol describes step-by-step instructions for processing, cells isolation, and culture of neonatal foreskin, with adaptation for more demanding adult tissues. The availability of multiple isogenic cell types derived from individual skin samples offers the ability to investigate various areas of biology, in the context of cell-type specificity without potential confounding influence of inter-individual or genetic differences. For complete details on the use and execution of this protocol, please refer to Holliman et al. (2017), Horvath et al. (2019), Horvath et al. (2018), Kabacik et al. (2018), Lowe et al. (2020), Lu et al. (2019), and Lu et al. (2018).
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spelling pubmed-91089812022-05-17 Isolation of five different primary cell types from a single sample of human skin Kabacik, Sylwia Lowe, Donna Cohen, Howard Felton, Sarah Spitzer, Joseph Raj, Ken STAR Protoc Protocol We have developed a technique to isolate primary keratinocytes, melanocytes, fibroblasts, preadipocytes, and microvascular endothelial cells from an individual sample of human skin. The protocol describes step-by-step instructions for processing, cells isolation, and culture of neonatal foreskin, with adaptation for more demanding adult tissues. The availability of multiple isogenic cell types derived from individual skin samples offers the ability to investigate various areas of biology, in the context of cell-type specificity without potential confounding influence of inter-individual or genetic differences. For complete details on the use and execution of this protocol, please refer to Holliman et al. (2017), Horvath et al. (2019), Horvath et al. (2018), Kabacik et al. (2018), Lowe et al. (2020), Lu et al. (2019), and Lu et al. (2018). Elsevier 2022-05-10 /pmc/articles/PMC9108981/ /pubmed/35586317 http://dx.doi.org/10.1016/j.xpro.2022.101378 Text en © 2022 The Authors 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
Kabacik, Sylwia
Lowe, Donna
Cohen, Howard
Felton, Sarah
Spitzer, Joseph
Raj, Ken
Isolation of five different primary cell types from a single sample of human skin
title Isolation of five different primary cell types from a single sample of human skin
title_full Isolation of five different primary cell types from a single sample of human skin
title_fullStr Isolation of five different primary cell types from a single sample of human skin
title_full_unstemmed Isolation of five different primary cell types from a single sample of human skin
title_short Isolation of five different primary cell types from a single sample of human skin
title_sort isolation of five different primary cell types from a single sample of human skin
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108981/
https://www.ncbi.nlm.nih.gov/pubmed/35586317
http://dx.doi.org/10.1016/j.xpro.2022.101378
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