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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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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. |
format | Online Article Text |
id | pubmed-4981906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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