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Enhanced isolation of lymphoid cells from human skin

Studying skin immune cells under various pathophysiological conditions is vital for understanding the nature of cutaneous inflammatory responses. Available methods of isolating cells from the skin have relatively low yield or require in vitro culture. To increase the effective isolation of skin immu...

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Autores principales: Salimi, M., Subramaniam, S., Selvakumar, T., Wang, X., Zemenides, S., Johnson, D., Ogg, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981906/
https://www.ncbi.nlm.nih.gov/pubmed/26805629
http://dx.doi.org/10.1111/ced.12802
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author Salimi, M.
Subramaniam, S.
Selvakumar, T.
Wang, X.
Zemenides, S.
Johnson, D.
Ogg, G.
author_facet Salimi, M.
Subramaniam, S.
Selvakumar, T.
Wang, X.
Zemenides, S.
Johnson, D.
Ogg, G.
author_sort Salimi, M.
collection PubMed
description Studying skin immune cells under various pathophysiological conditions is vital for understanding the nature of cutaneous inflammatory responses. Available methods of isolating cells from the skin have relatively low yield or require in vitro culture. To increase the effective isolation of skin immune cells, we used collagenase P treatment. The number of T cells obtained ex vivo using this technique was dramatically greater than that obtained with conventional methods, without the need for long‐term culture. The phenotype and function of isolated cells were comparable with those of cells isolated by EDTA treatment. Collagenase P‐based methods will enhance the ability to investigate lymphoid cell function in both healthy and diseased skin.
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spelling pubmed-49819062016-08-26 Enhanced isolation of lymphoid cells from human skin Salimi, M. Subramaniam, S. Selvakumar, T. Wang, X. Zemenides, S. Johnson, D. Ogg, G. Clin Exp Dermatol Experimental Dermatology Studying skin immune cells under various pathophysiological conditions is vital for understanding the nature of cutaneous inflammatory responses. Available methods of isolating cells from the skin have relatively low yield or require in vitro culture. To increase the effective isolation of skin immune cells, we used collagenase P treatment. The number of T cells obtained ex vivo using this technique was dramatically greater than that obtained with conventional methods, without the need for long‐term culture. The phenotype and function of isolated cells were comparable with those of cells isolated by EDTA treatment. Collagenase P‐based methods will enhance the ability to investigate lymphoid cell function in both healthy and diseased skin. John Wiley and Sons Inc. 2016-01-25 2016-07 /pmc/articles/PMC4981906/ /pubmed/26805629 http://dx.doi.org/10.1111/ced.12802 Text en © 2016 The Authors Clinical and Experimental Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists, North American Clinical Dermatologic Society and St Johns Dermatological Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Experimental Dermatology
Salimi, M.
Subramaniam, S.
Selvakumar, T.
Wang, X.
Zemenides, S.
Johnson, D.
Ogg, G.
Enhanced isolation of lymphoid cells from human skin
title Enhanced isolation of lymphoid cells from human skin
title_full Enhanced isolation of lymphoid cells from human skin
title_fullStr Enhanced isolation of lymphoid cells from human skin
title_full_unstemmed Enhanced isolation of lymphoid cells from human skin
title_short Enhanced isolation of lymphoid cells from human skin
title_sort enhanced isolation of lymphoid cells from human skin
topic Experimental Dermatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981906/
https://www.ncbi.nlm.nih.gov/pubmed/26805629
http://dx.doi.org/10.1111/ced.12802
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