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Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system

Macrophage colony-stimulating factor (CSF1) is an essential growth factor to control the proliferation, differentiation and survival of cells of the macrophage lineage in vertebrates. We have previously produced a recombinant chicken CSF1-Fc fusion protein and administrated it to birds which produce...

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Autores principales: Wu, Zhiguang, Harne, Rakhi, Chintoan-Uta, Cosmin, Hu, Tuan-Jun, Wallace, Robert, MacCallum, Amanda, Stevens, Mark P., Kaiser, Pete, Balic, Adam, Hume, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996135/
https://www.ncbi.nlm.nih.gov/pubmed/31870792
http://dx.doi.org/10.1016/j.dci.2019.103586
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author Wu, Zhiguang
Harne, Rakhi
Chintoan-Uta, Cosmin
Hu, Tuan-Jun
Wallace, Robert
MacCallum, Amanda
Stevens, Mark P.
Kaiser, Pete
Balic, Adam
Hume, David A.
author_facet Wu, Zhiguang
Harne, Rakhi
Chintoan-Uta, Cosmin
Hu, Tuan-Jun
Wallace, Robert
MacCallum, Amanda
Stevens, Mark P.
Kaiser, Pete
Balic, Adam
Hume, David A.
author_sort Wu, Zhiguang
collection PubMed
description Macrophage colony-stimulating factor (CSF1) is an essential growth factor to control the proliferation, differentiation and survival of cells of the macrophage lineage in vertebrates. We have previously produced a recombinant chicken CSF1-Fc fusion protein and administrated it to birds which produced a substantial expansion of tissue macrophage populations. To further study the biology of CSF1 in the chicken, here we generated anti-chicken CSF1 antibodies (ROS-AV181 and 183) using CSF1-Fc as an immunogen. The specific binding of each monoclonal antibody was confirmed by ELISA, Western blotting and immunohistochemistry on tissue sections. Using the anti-CSF1 antibodies, we show that chicken bone marrow derived macrophages (BMDM) express CSF1 on their surface, and that the level appears to be regulated further by exogenous CSF1. By capture ELISA circulating CSF1 levels increased transiently in both layer and broiler embryos around the day of hatch. The levels of CSF1 in broilers was higher than in layers during the first week after hatch. Antibody ROS-AV183 was able to block CSF1 biological activity in vitro and treatment of hatchlings using this neutralising antibody in vivo impacted on some tissue macrophage populations, but not blood monocytes. After anti-CSF1 treatment, CSF1R-transgene reporter expressing cells were reduced in the bursa of Fabricius and cecal tonsil and TIM4(+) Kupffer cells in the liver were almost completely ablated. Anti-CSF1 treatment also produced a reduction in overall bone density, trabecular volume and TRAP(+) osteoclasts. Our novel neutralising antibody provides a new tool to study the roles of CSF1 in birds.
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spelling pubmed-69961352020-04-01 Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system Wu, Zhiguang Harne, Rakhi Chintoan-Uta, Cosmin Hu, Tuan-Jun Wallace, Robert MacCallum, Amanda Stevens, Mark P. Kaiser, Pete Balic, Adam Hume, David A. Dev Comp Immunol Article Macrophage colony-stimulating factor (CSF1) is an essential growth factor to control the proliferation, differentiation and survival of cells of the macrophage lineage in vertebrates. We have previously produced a recombinant chicken CSF1-Fc fusion protein and administrated it to birds which produced a substantial expansion of tissue macrophage populations. To further study the biology of CSF1 in the chicken, here we generated anti-chicken CSF1 antibodies (ROS-AV181 and 183) using CSF1-Fc as an immunogen. The specific binding of each monoclonal antibody was confirmed by ELISA, Western blotting and immunohistochemistry on tissue sections. Using the anti-CSF1 antibodies, we show that chicken bone marrow derived macrophages (BMDM) express CSF1 on their surface, and that the level appears to be regulated further by exogenous CSF1. By capture ELISA circulating CSF1 levels increased transiently in both layer and broiler embryos around the day of hatch. The levels of CSF1 in broilers was higher than in layers during the first week after hatch. Antibody ROS-AV183 was able to block CSF1 biological activity in vitro and treatment of hatchlings using this neutralising antibody in vivo impacted on some tissue macrophage populations, but not blood monocytes. After anti-CSF1 treatment, CSF1R-transgene reporter expressing cells were reduced in the bursa of Fabricius and cecal tonsil and TIM4(+) Kupffer cells in the liver were almost completely ablated. Anti-CSF1 treatment also produced a reduction in overall bone density, trabecular volume and TRAP(+) osteoclasts. Our novel neutralising antibody provides a new tool to study the roles of CSF1 in birds. Elsevier Science 2020-04 /pmc/articles/PMC6996135/ /pubmed/31870792 http://dx.doi.org/10.1016/j.dci.2019.103586 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wu, Zhiguang
Harne, Rakhi
Chintoan-Uta, Cosmin
Hu, Tuan-Jun
Wallace, Robert
MacCallum, Amanda
Stevens, Mark P.
Kaiser, Pete
Balic, Adam
Hume, David A.
Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system
title Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system
title_full Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system
title_fullStr Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system
title_full_unstemmed Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system
title_short Regulation and function of macrophage colony-stimulating factor (CSF1) in the chicken immune system
title_sort regulation and function of macrophage colony-stimulating factor (csf1) in the chicken immune system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996135/
https://www.ncbi.nlm.nih.gov/pubmed/31870792
http://dx.doi.org/10.1016/j.dci.2019.103586
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