Developmental control of macrophage function

被引:67
作者
Bonnardel, Johnny [1 ,2 ]
Guilliams, Martin [1 ,2 ]
机构
[1] VIB Ctr Inflammat Res, Lab Myeloid Cell Ontogeny & Funct Specialisat, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, Ghent, Belgium
基金
欧洲研究理事会; 欧盟地平线“2020”;
关键词
TISSUE-RESIDENT MACROPHAGES; HEMATOPOIETIC STEM-CELLS; COLONY-STIMULATING FACTOR; CENTRAL-NERVOUS-SYSTEM; DENDRITIC CELLS; CIRCULATING MONOCYTES; ALVEOLAR MACROPHAGES; BACTERIAL-INFECTION; LY6C(LOW) MONOCYTES; CARDIAC MACROPHAGES;
D O I
10.1016/j.coi.2017.12.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The combination between novel fate-mapping tools and single cell RNA-sequencing technology has revealed the presence of multiple macrophage progenitors. This raises the fascinating possibility that what was once perceived as immense functional plasticity of macrophages could in fact come down to separate macrophage subsets performing distinct functions because of their differential cellular origin. The question of macrophage plasticity versus macrophage heterogeneity is broader than the difference between macrophages of embryonic or adult hematopoietic origin and is particularly relevant in the context of inflammation. In this manuscript, we review the potential impact of cellular origin on the function of macrophages. We also highlight the need for novel 'functional fate-mapping' tools that would reveal the history of the functional state of macrophages, rather than their cellular origin, in order to finally study their true plasticity in vivo.
引用
收藏
页码:64 / 74
页数:11
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