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Ly6G-mediated depletion of neutrophils is dependent on macrophages
Antibody-mediated depletion of neutrophils is commonly used to study neutropenia. However, the mechanisms by which antibodies deplete neutrophils have not been well defined. We noticed that mice deficient in complement and macrophages had blunted neutrophil depletion in response to anti-Ly6G monoclo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711394/ https://www.ncbi.nlm.nih.gov/pubmed/26870635 http://dx.doi.org/10.1016/j.rinim.2015.12.001 |
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author | Bruhn, Kevin W. Dekitani, Ken Nielsen, Travis B. Pantapalangkoor, Paul Spellberg, Brad |
author_facet | Bruhn, Kevin W. Dekitani, Ken Nielsen, Travis B. Pantapalangkoor, Paul Spellberg, Brad |
author_sort | Bruhn, Kevin W. |
collection | PubMed |
description | Antibody-mediated depletion of neutrophils is commonly used to study neutropenia. However, the mechanisms by which antibodies deplete neutrophils have not been well defined. We noticed that mice deficient in complement and macrophages had blunted neutrophil depletion in response to anti-Ly6G monoclonal antibody (MAb) treatment. In vitro, exposure of murine neutrophils to anti-Ly6G MAb in the presence of plasma did not result in significant depletion of cells, either in the presence or absence of complement. In vivo, anti-Ly6G-mediated neutrophil depletion was abrogated following macrophage depletion, but not complement depletion, indicating a requirement for macrophages to induce neutropenia by this method. These results inform the use and limitations of anti-Ly6G antibody as an experimental tool for depleting neutrophils in various immunological settings. |
format | Online Article Text |
id | pubmed-4711394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-47113942016-02-11 Ly6G-mediated depletion of neutrophils is dependent on macrophages Bruhn, Kevin W. Dekitani, Ken Nielsen, Travis B. Pantapalangkoor, Paul Spellberg, Brad Results Immunol Micro Article Antibody-mediated depletion of neutrophils is commonly used to study neutropenia. However, the mechanisms by which antibodies deplete neutrophils have not been well defined. We noticed that mice deficient in complement and macrophages had blunted neutrophil depletion in response to anti-Ly6G monoclonal antibody (MAb) treatment. In vitro, exposure of murine neutrophils to anti-Ly6G MAb in the presence of plasma did not result in significant depletion of cells, either in the presence or absence of complement. In vivo, anti-Ly6G-mediated neutrophil depletion was abrogated following macrophage depletion, but not complement depletion, indicating a requirement for macrophages to induce neutropenia by this method. These results inform the use and limitations of anti-Ly6G antibody as an experimental tool for depleting neutrophils in various immunological settings. Elsevier 2015-12-21 /pmc/articles/PMC4711394/ /pubmed/26870635 http://dx.doi.org/10.1016/j.rinim.2015.12.001 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Micro Article Bruhn, Kevin W. Dekitani, Ken Nielsen, Travis B. Pantapalangkoor, Paul Spellberg, Brad Ly6G-mediated depletion of neutrophils is dependent on macrophages |
title | Ly6G-mediated depletion of neutrophils is dependent on macrophages |
title_full | Ly6G-mediated depletion of neutrophils is dependent on macrophages |
title_fullStr | Ly6G-mediated depletion of neutrophils is dependent on macrophages |
title_full_unstemmed | Ly6G-mediated depletion of neutrophils is dependent on macrophages |
title_short | Ly6G-mediated depletion of neutrophils is dependent on macrophages |
title_sort | ly6g-mediated depletion of neutrophils is dependent on macrophages |
topic | Micro Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711394/ https://www.ncbi.nlm.nih.gov/pubmed/26870635 http://dx.doi.org/10.1016/j.rinim.2015.12.001 |
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