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Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes
Mononuclear phagocytes are present in skin and mucosa and represent one of the first lines of defense against invading pathogens, which they detect via an array of pathogen-binding receptors expressed on their surface. However, their extraction from tissue is difficult, and the isolation technique u...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Leukocyte Biology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433859/ https://www.ncbi.nlm.nih.gov/pubmed/28270408 http://dx.doi.org/10.1189/jlb.4A1116-496R |
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author | Botting, Rachel A. Bertram, Kirstie M. Baharlou, Heeva Sandgren, Kerrie J. Fletcher, James Rhodes, Jake W. Rana, Hafsa Plasto, Toby M. Wang, Xin Maggie Lim, Jake J. K. Barnouti, Laith Kohout, Mark P. Papadopoulos, Tim Merten, Steve Olbourne, Norman Cunningham, Anthony L. Haniffa, Muzlifah Harman, Andrew N. |
author_facet | Botting, Rachel A. Bertram, Kirstie M. Baharlou, Heeva Sandgren, Kerrie J. Fletcher, James Rhodes, Jake W. Rana, Hafsa Plasto, Toby M. Wang, Xin Maggie Lim, Jake J. K. Barnouti, Laith Kohout, Mark P. Papadopoulos, Tim Merten, Steve Olbourne, Norman Cunningham, Anthony L. Haniffa, Muzlifah Harman, Andrew N. |
author_sort | Botting, Rachel A. |
collection | PubMed |
description | Mononuclear phagocytes are present in skin and mucosa and represent one of the first lines of defense against invading pathogens, which they detect via an array of pathogen-binding receptors expressed on their surface. However, their extraction from tissue is difficult, and the isolation technique used has functional consequences on the cells obtained. Here, we compare mononuclear phagocytes isolated from human skin using either enzymatic digestion or spontaneous migration. Cells isolated via enzymatic digestion are in an immature state, and all subsets are easily defined. However, cells isolated by spontaneous migration are in a mature state, and CD141 cross-presenting DCs (cDC1) are more difficult to define. Different pathogen-binding receptors are susceptible to cleavage by blends of collagenase, demonstrating that great care must be taken in choosing the correct enzyme blend to digest tissue if carrying out pathogen-interaction assays. Finally, we have optimized mononuclear phagocyte culture conditions to enhance their survival after liberation from the tissue. |
format | Online Article Text |
id | pubmed-5433859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Society for Leukocyte Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-54338592017-05-18 Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes Botting, Rachel A. Bertram, Kirstie M. Baharlou, Heeva Sandgren, Kerrie J. Fletcher, James Rhodes, Jake W. Rana, Hafsa Plasto, Toby M. Wang, Xin Maggie Lim, Jake J. K. Barnouti, Laith Kohout, Mark P. Papadopoulos, Tim Merten, Steve Olbourne, Norman Cunningham, Anthony L. Haniffa, Muzlifah Harman, Andrew N. J Leukoc Biol Host Defense & Pathophysiology Mononuclear phagocytes are present in skin and mucosa and represent one of the first lines of defense against invading pathogens, which they detect via an array of pathogen-binding receptors expressed on their surface. However, their extraction from tissue is difficult, and the isolation technique used has functional consequences on the cells obtained. Here, we compare mononuclear phagocytes isolated from human skin using either enzymatic digestion or spontaneous migration. Cells isolated via enzymatic digestion are in an immature state, and all subsets are easily defined. However, cells isolated by spontaneous migration are in a mature state, and CD141 cross-presenting DCs (cDC1) are more difficult to define. Different pathogen-binding receptors are susceptible to cleavage by blends of collagenase, demonstrating that great care must be taken in choosing the correct enzyme blend to digest tissue if carrying out pathogen-interaction assays. Finally, we have optimized mononuclear phagocyte culture conditions to enhance their survival after liberation from the tissue. Society for Leukocyte Biology 2017-06 2017-03-07 /pmc/articles/PMC5433859/ /pubmed/28270408 http://dx.doi.org/10.1189/jlb.4A1116-496R Text en © The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Host Defense & Pathophysiology Botting, Rachel A. Bertram, Kirstie M. Baharlou, Heeva Sandgren, Kerrie J. Fletcher, James Rhodes, Jake W. Rana, Hafsa Plasto, Toby M. Wang, Xin Maggie Lim, Jake J. K. Barnouti, Laith Kohout, Mark P. Papadopoulos, Tim Merten, Steve Olbourne, Norman Cunningham, Anthony L. Haniffa, Muzlifah Harman, Andrew N. Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes |
title | Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes |
title_full | Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes |
title_fullStr | Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes |
title_full_unstemmed | Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes |
title_short | Phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes |
title_sort | phenotypic and functional consequences of different isolation protocols on skin mononuclear phagocytes |
topic | Host Defense & Pathophysiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433859/ https://www.ncbi.nlm.nih.gov/pubmed/28270408 http://dx.doi.org/10.1189/jlb.4A1116-496R |
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