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Macrophage heterogeneity in tissues: phenotypic diversity and functions.

作者信息

Gordon Siamon, Plüddemann Annette, Martinez Estrada Fernando

机构信息

Sir William Dunn School of Pathology, University of Oxford, Oxford, UK.

出版信息

Immunol Rev. 2014 Nov;262(1):36-55. doi: 10.1111/imr.12223.


DOI:10.1111/imr.12223
PMID:25319326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4231239/
Abstract

During development and throughout adult life, macrophages derived from hematopoietic progenitors are seeded throughout the body, initially in the absence of inflammatory and infectious stimuli as tissue-resident cells, with enhanced recruitment, activation, and local proliferation following injury and pathologic insults. We have learned a great deal about macrophage properties ex vivo and in cell culture, but their phenotypic heterogeneity within different tissue microenvironments remains poorly characterized, although it contributes significantly to maintaining local and systemic homeostasis, pathogenesis, and possible treatment. In this review, we summarize the nature, functions, and interactions of tissue macrophage populations within their microenvironment and suggest questions for further investigation.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/8fcaf7f1ce77/imr0262-0036-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/4b7315adf760/imr0262-0036-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/65856219159d/imr0262-0036-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/643cd493594c/imr0262-0036-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/8fcaf7f1ce77/imr0262-0036-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/4b7315adf760/imr0262-0036-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/65856219159d/imr0262-0036-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/643cd493594c/imr0262-0036-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e132/4231239/8fcaf7f1ce77/imr0262-0036-f4.jpg

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本文引用的文献

[1]
Macrophage activation and polarization: nomenclature and experimental guidelines.

Immunity. 2014-7-17

[2]
Gata6 regulates aspartoacylase expression in resident peritoneal macrophages and controls their survival.

J Exp Med. 2014-7-14

[3]
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J Exp Med. 2014-7-7

[4]
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Circ Res. 2014-6-6

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Nat Rev Immunol. 2014-6

[6]
Inhibition of UDP/P2Y6 purinergic signaling prevents phagocytosis of viable neurons by activated microglia in vitro and in vivo.

Glia. 2014-5-19

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Cell. 2014-5-1

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Cell Immunol. 2014-4-8

[9]
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Immunology. 2014-9

[10]
The transcription factor Gata6 links tissue macrophage phenotype and proliferative renewal.

Science. 2014-4-24

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