Journal article 734 views 93 downloads
Tissue‐resident macrophages: then and now
Immunology, Volume: 144, Issue: 4, Pages: 541 - 548
Swansea University Author: Luke Davies
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Copyright: 2015 The Authors. This is an open access article under the terms of the Creative Commons Attribution License
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DOI (Published version): 10.1111/imm.12451
Abstract
Macrophages have been at the heart of immune research for over a century and are an integral component of innate immunity. Macrophages are often viewed as terminally differentiated monocytic phagocytes. They infiltrate tissues during inflammation, and form polarized populations that perform pro-infl...
Published in: | Immunology |
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ISSN: | 0019-2805 1365-2567 |
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Wiley
2015
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URI: | https://cronfa.swan.ac.uk/Record/cronfa61706 |
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2022-11-07T11:01:09.4711220 v2 61706 2022-10-31 Tissue‐resident macrophages: then and now ff080296775381560053d5e3a6e81745 0000-0001-7767-4060 Luke Davies Luke Davies true false 2022-10-31 BMS Macrophages have been at the heart of immune research for over a century and are an integral component of innate immunity. Macrophages are often viewed as terminally differentiated monocytic phagocytes. They infiltrate tissues during inflammation, and form polarized populations that perform pro-inflammatory or anti-inflammatory functions. Tissue-resident macrophages were regarded as differentiated monocytes, which seed the tissues to perform immune sentinel and homeostatic functions. However, tissue-resident macrophages are not a homogeneous population, but are in fact a grouping of cells with similar functions and phenotypes. In the last decade, it has been revealed that many of these cells are not terminally differentiated and, in most cases, are not derived from haematopoiesis in the adult. Recent research has highlighted that tissue-resident macrophages cannot be grouped into simple polarized categories, especially in vivo, when they are exposed to complex signalling events. It has now been demonstrated that the tissue environment itself is a major controller of macrophage phenotype, and can influence the expression of many genes regardless of origin. This is consistent with the concept that cells within different tissues have diverse responses in inflammation. There is still a mountain to climb in the field, as it evolves to encompass not only tissue-resident macrophage diversity, but also categorization of specific tissue environments and the plasticity of macrophages themselves. This knowledge provides a new perspective on therapeutic strategies, as macrophage subsets can potentially be manipulated to control the inflammatory environment in a tissue-specific manner. Journal Article Immunology 144 4 541 548 Wiley 0019-2805 1365-2567 environmental programming; Gata6; tissue-resident macrophages 1 4 2015 2015-04-01 10.1111/imm.12451 COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University Medical Research Council; Wellcome Trust Institutional Strategic Support Fund; LEI; National Cancer Institute; National Institutes of Health; Intramural Research Program USA; Medical Research Council UK 2022-11-07T11:01:09.4711220 2022-10-31T12:40:39.0439264 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Luke Davies 0000-0001-7767-4060 1 Philip R. Taylor 2 61706__25663__e9046a6e7d1d44ea86a00e6796aa8857.pdf 61706.pdf 2022-11-07T11:00:04.9568561 Output 396014 application/pdf Version of Record true Copyright: 2015 The Authors. This is an open access article under the terms of the Creative Commons Attribution License true eng http://creativecommons.org/licenses/by/4.0/ |
title |
Tissue‐resident macrophages: then and now |
spellingShingle |
Tissue‐resident macrophages: then and now Luke Davies |
title_short |
Tissue‐resident macrophages: then and now |
title_full |
Tissue‐resident macrophages: then and now |
title_fullStr |
Tissue‐resident macrophages: then and now |
title_full_unstemmed |
Tissue‐resident macrophages: then and now |
title_sort |
Tissue‐resident macrophages: then and now |
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ff080296775381560053d5e3a6e81745 |
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ff080296775381560053d5e3a6e81745_***_Luke Davies |
author |
Luke Davies |
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Luke Davies Philip R. Taylor |
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Immunology |
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144 |
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541 |
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2015 |
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Swansea University |
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0019-2805 1365-2567 |
doi_str_mv |
10.1111/imm.12451 |
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Wiley |
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Faculty of Medicine, Health and Life Sciences |
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description |
Macrophages have been at the heart of immune research for over a century and are an integral component of innate immunity. Macrophages are often viewed as terminally differentiated monocytic phagocytes. They infiltrate tissues during inflammation, and form polarized populations that perform pro-inflammatory or anti-inflammatory functions. Tissue-resident macrophages were regarded as differentiated monocytes, which seed the tissues to perform immune sentinel and homeostatic functions. However, tissue-resident macrophages are not a homogeneous population, but are in fact a grouping of cells with similar functions and phenotypes. In the last decade, it has been revealed that many of these cells are not terminally differentiated and, in most cases, are not derived from haematopoiesis in the adult. Recent research has highlighted that tissue-resident macrophages cannot be grouped into simple polarized categories, especially in vivo, when they are exposed to complex signalling events. It has now been demonstrated that the tissue environment itself is a major controller of macrophage phenotype, and can influence the expression of many genes regardless of origin. This is consistent with the concept that cells within different tissues have diverse responses in inflammation. There is still a mountain to climb in the field, as it evolves to encompass not only tissue-resident macrophage diversity, but also categorization of specific tissue environments and the plasticity of macrophages themselves. This knowledge provides a new perspective on therapeutic strategies, as macrophage subsets can potentially be manipulated to control the inflammatory environment in a tissue-specific manner. |
published_date |
2015-04-01T04:20:43Z |
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1763754370735800320 |
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11.03559 |