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Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions

BACKGROUND: Infectious diseases of farmed and wild animals pose a recurrent threat to food security and human health. The macrophage, a key component of the innate immune system, is the first line of defence against many infectious agents and plays a major role in shaping the adaptive immune respons...

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Autores principales: Meek, Stephen, Watson, Tom, Eory, Lel, McFarlane, Gus, Wynne, Felicity J., McCleary, Stephen, Dunn, Laura E. M., Charlton, Emily M., Craig, Chloe, Shih, Barbara, Regan, Tim, Taylor, Ryan, Sutherland, Linda, Gossner, Anton, Chintoan-Uta, Cosmin, Fletcher, Sarah, Beard, Philippa M., Hassan, Musa A., Grey, Finn, Hope, Jayne C., Stevens, Mark P., Nowak-Imialek, Monika, Niemann, Heiner, Ross, Pablo J., Tait-Burkard, Christine, Brown, Sarah M., Lefevre, Lucas, Thomson, Gerard, McColl, Barry W., Lawrence, Alistair B., Archibald, Alan L., Steinbach, Falko, Crooke, Helen R., Gao, Xuefei, Liu, Pentao, Burdon, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759257/
https://www.ncbi.nlm.nih.gov/pubmed/35027054
http://dx.doi.org/10.1186/s12915-021-01217-8
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author Meek, Stephen
Watson, Tom
Eory, Lel
McFarlane, Gus
Wynne, Felicity J.
McCleary, Stephen
Dunn, Laura E. M.
Charlton, Emily M.
Craig, Chloe
Shih, Barbara
Regan, Tim
Taylor, Ryan
Sutherland, Linda
Gossner, Anton
Chintoan-Uta, Cosmin
Fletcher, Sarah
Beard, Philippa M.
Hassan, Musa A.
Grey, Finn
Hope, Jayne C.
Stevens, Mark P.
Nowak-Imialek, Monika
Niemann, Heiner
Ross, Pablo J.
Tait-Burkard, Christine
Brown, Sarah M.
Lefevre, Lucas
Thomson, Gerard
McColl, Barry W.
Lawrence, Alistair B.
Archibald, Alan L.
Steinbach, Falko
Crooke, Helen R.
Gao, Xuefei
Liu, Pentao
Burdon, Tom
author_facet Meek, Stephen
Watson, Tom
Eory, Lel
McFarlane, Gus
Wynne, Felicity J.
McCleary, Stephen
Dunn, Laura E. M.
Charlton, Emily M.
Craig, Chloe
Shih, Barbara
Regan, Tim
Taylor, Ryan
Sutherland, Linda
Gossner, Anton
Chintoan-Uta, Cosmin
Fletcher, Sarah
Beard, Philippa M.
Hassan, Musa A.
Grey, Finn
Hope, Jayne C.
Stevens, Mark P.
Nowak-Imialek, Monika
Niemann, Heiner
Ross, Pablo J.
Tait-Burkard, Christine
Brown, Sarah M.
Lefevre, Lucas
Thomson, Gerard
McColl, Barry W.
Lawrence, Alistair B.
Archibald, Alan L.
Steinbach, Falko
Crooke, Helen R.
Gao, Xuefei
Liu, Pentao
Burdon, Tom
author_sort Meek, Stephen
collection PubMed
description BACKGROUND: Infectious diseases of farmed and wild animals pose a recurrent threat to food security and human health. The macrophage, a key component of the innate immune system, is the first line of defence against many infectious agents and plays a major role in shaping the adaptive immune response. However, this phagocyte is a target and host for many pathogens. Understanding the molecular basis of interactions between macrophages and pathogens is therefore crucial for the development of effective strategies to combat important infectious diseases. RESULTS: We explored how porcine pluripotent stem cells (PSCs) can provide a limitless in vitro supply of genetically and experimentally tractable macrophages. Porcine PSC-derived macrophages (PSCdMs) exhibited molecular and functional characteristics of ex vivo primary macrophages and were productively infected by pig pathogens, including porcine reproductive and respiratory syndrome virus (PRRSV) and African swine fever virus (ASFV), two of the most economically important and devastating viruses in pig farming. Moreover, porcine PSCdMs were readily amenable to genetic modification by CRISPR/Cas9 gene editing applied either in parental stem cells or directly in the macrophages by lentiviral vector transduction. CONCLUSIONS: We show that porcine PSCdMs exhibit key macrophage characteristics, including infection by a range of commercially relevant pig pathogens. In addition, genetic engineering of PSCs and PSCdMs affords new opportunities for functional analysis of macrophage biology in an important livestock species. PSCs and differentiated derivatives should therefore represent a useful and ethical experimental platform to investigate the genetic and molecular basis of host-pathogen interactions in pigs, and also have wider applications in livestock. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01217-8.
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spelling pubmed-87592572022-01-18 Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions Meek, Stephen Watson, Tom Eory, Lel McFarlane, Gus Wynne, Felicity J. McCleary, Stephen Dunn, Laura E. M. Charlton, Emily M. Craig, Chloe Shih, Barbara Regan, Tim Taylor, Ryan Sutherland, Linda Gossner, Anton Chintoan-Uta, Cosmin Fletcher, Sarah Beard, Philippa M. Hassan, Musa A. Grey, Finn Hope, Jayne C. Stevens, Mark P. Nowak-Imialek, Monika Niemann, Heiner Ross, Pablo J. Tait-Burkard, Christine Brown, Sarah M. Lefevre, Lucas Thomson, Gerard McColl, Barry W. Lawrence, Alistair B. Archibald, Alan L. Steinbach, Falko Crooke, Helen R. Gao, Xuefei Liu, Pentao Burdon, Tom BMC Biol Methodology Article BACKGROUND: Infectious diseases of farmed and wild animals pose a recurrent threat to food security and human health. The macrophage, a key component of the innate immune system, is the first line of defence against many infectious agents and plays a major role in shaping the adaptive immune response. However, this phagocyte is a target and host for many pathogens. Understanding the molecular basis of interactions between macrophages and pathogens is therefore crucial for the development of effective strategies to combat important infectious diseases. RESULTS: We explored how porcine pluripotent stem cells (PSCs) can provide a limitless in vitro supply of genetically and experimentally tractable macrophages. Porcine PSC-derived macrophages (PSCdMs) exhibited molecular and functional characteristics of ex vivo primary macrophages and were productively infected by pig pathogens, including porcine reproductive and respiratory syndrome virus (PRRSV) and African swine fever virus (ASFV), two of the most economically important and devastating viruses in pig farming. Moreover, porcine PSCdMs were readily amenable to genetic modification by CRISPR/Cas9 gene editing applied either in parental stem cells or directly in the macrophages by lentiviral vector transduction. CONCLUSIONS: We show that porcine PSCdMs exhibit key macrophage characteristics, including infection by a range of commercially relevant pig pathogens. In addition, genetic engineering of PSCs and PSCdMs affords new opportunities for functional analysis of macrophage biology in an important livestock species. PSCs and differentiated derivatives should therefore represent a useful and ethical experimental platform to investigate the genetic and molecular basis of host-pathogen interactions in pigs, and also have wider applications in livestock. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01217-8. BioMed Central 2022-01-14 /pmc/articles/PMC8759257/ /pubmed/35027054 http://dx.doi.org/10.1186/s12915-021-01217-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Meek, Stephen
Watson, Tom
Eory, Lel
McFarlane, Gus
Wynne, Felicity J.
McCleary, Stephen
Dunn, Laura E. M.
Charlton, Emily M.
Craig, Chloe
Shih, Barbara
Regan, Tim
Taylor, Ryan
Sutherland, Linda
Gossner, Anton
Chintoan-Uta, Cosmin
Fletcher, Sarah
Beard, Philippa M.
Hassan, Musa A.
Grey, Finn
Hope, Jayne C.
Stevens, Mark P.
Nowak-Imialek, Monika
Niemann, Heiner
Ross, Pablo J.
Tait-Burkard, Christine
Brown, Sarah M.
Lefevre, Lucas
Thomson, Gerard
McColl, Barry W.
Lawrence, Alistair B.
Archibald, Alan L.
Steinbach, Falko
Crooke, Helen R.
Gao, Xuefei
Liu, Pentao
Burdon, Tom
Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions
title Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions
title_full Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions
title_fullStr Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions
title_full_unstemmed Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions
title_short Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions
title_sort stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759257/
https://www.ncbi.nlm.nih.gov/pubmed/35027054
http://dx.doi.org/10.1186/s12915-021-01217-8
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