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A lesson from the wild: The natural state of eosinophils is Ly6G(hi)
With a long history of promoting pathological inflammation, eosinophils are now emerging as important regulatory cells. Yet, findings from controlled laboratory experiments so far lack translation to animals, including humans, in their natural environment. In order to appreciate the breadth of eosin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561109/ https://www.ncbi.nlm.nih.gov/pubmed/34486729 http://dx.doi.org/10.1111/imm.13413 |
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author | Mair, Iris Wolfenden, Andrew Lowe, Ann E. Bennett, Alex Muir, Andrew Smith, Hannah Fenn, Jonathan Bradley, Janette E. Else, Kathryn J. |
author_facet | Mair, Iris Wolfenden, Andrew Lowe, Ann E. Bennett, Alex Muir, Andrew Smith, Hannah Fenn, Jonathan Bradley, Janette E. Else, Kathryn J. |
author_sort | Mair, Iris |
collection | PubMed |
description | With a long history of promoting pathological inflammation, eosinophils are now emerging as important regulatory cells. Yet, findings from controlled laboratory experiments so far lack translation to animals, including humans, in their natural environment. In order to appreciate the breadth of eosinophil phenotype under non‐laboratory, uncontrolled conditions, we exploit a free‐living population of the model organism Mus musculus domesticus. Eosinophils were present at significantly higher proportions in the spleen and bone marrow of wild mice compared with laboratory mice. Strikingly, the majority of eosinophils of wild mice exhibited a unique Ly6G(hi) phenotype seldom described in laboratory literature. Ly6G expression correlated with activation status in spleen and bone marrow, but not peritoneal exudate cells, and is therefore likely not an activation marker per se. Intermediate Ly6G expression was transiently induced in a small proportion of eosinophils from C57BL/6 laboratory mice during acute infection with the whipworm Trichuris muris, but not during low‐dose chronic infection, which better represents parasite exposure in the wild. We conclude that the natural state of the eosinophil is not adequately reflected in the standard laboratory mouse, which compromises our attempts to dissect their functional relevance. Our findings emphasize the importance of studying the immune system in its natural context – alongside more mechanistic laboratory experiments – in order to capture the entirety of immune phenotypes and functions. |
format | Online Article Text |
id | pubmed-8561109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85611092021-11-08 A lesson from the wild: The natural state of eosinophils is Ly6G(hi) Mair, Iris Wolfenden, Andrew Lowe, Ann E. Bennett, Alex Muir, Andrew Smith, Hannah Fenn, Jonathan Bradley, Janette E. Else, Kathryn J. Immunology Original Articles With a long history of promoting pathological inflammation, eosinophils are now emerging as important regulatory cells. Yet, findings from controlled laboratory experiments so far lack translation to animals, including humans, in their natural environment. In order to appreciate the breadth of eosinophil phenotype under non‐laboratory, uncontrolled conditions, we exploit a free‐living population of the model organism Mus musculus domesticus. Eosinophils were present at significantly higher proportions in the spleen and bone marrow of wild mice compared with laboratory mice. Strikingly, the majority of eosinophils of wild mice exhibited a unique Ly6G(hi) phenotype seldom described in laboratory literature. Ly6G expression correlated with activation status in spleen and bone marrow, but not peritoneal exudate cells, and is therefore likely not an activation marker per se. Intermediate Ly6G expression was transiently induced in a small proportion of eosinophils from C57BL/6 laboratory mice during acute infection with the whipworm Trichuris muris, but not during low‐dose chronic infection, which better represents parasite exposure in the wild. We conclude that the natural state of the eosinophil is not adequately reflected in the standard laboratory mouse, which compromises our attempts to dissect their functional relevance. Our findings emphasize the importance of studying the immune system in its natural context – alongside more mechanistic laboratory experiments – in order to capture the entirety of immune phenotypes and functions. John Wiley and Sons Inc. 2021-09-15 2021-12 /pmc/articles/PMC8561109/ /pubmed/34486729 http://dx.doi.org/10.1111/imm.13413 Text en © 2021 The Authors. Immunology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Mair, Iris Wolfenden, Andrew Lowe, Ann E. Bennett, Alex Muir, Andrew Smith, Hannah Fenn, Jonathan Bradley, Janette E. Else, Kathryn J. A lesson from the wild: The natural state of eosinophils is Ly6G(hi) |
title | A lesson from the wild: The natural state of eosinophils is Ly6G(hi)
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title_full | A lesson from the wild: The natural state of eosinophils is Ly6G(hi)
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title_fullStr | A lesson from the wild: The natural state of eosinophils is Ly6G(hi)
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title_full_unstemmed | A lesson from the wild: The natural state of eosinophils is Ly6G(hi)
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title_short | A lesson from the wild: The natural state of eosinophils is Ly6G(hi)
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title_sort | lesson from the wild: the natural state of eosinophils is ly6g(hi) |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561109/ https://www.ncbi.nlm.nih.gov/pubmed/34486729 http://dx.doi.org/10.1111/imm.13413 |
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