Ontogeny and homeostasis of CNS myeloid cells

被引:312
作者
Prinz, Marco [1 ,2 ]
Erny, Daniel [1 ,3 ]
Hagemeyer, Nora [1 ]
机构
[1] Univ Freiburg, Inst Neuropathol, Fac Med, Freiburg, Germany
[2] Univ Freiburg, BIOSS Ctr Biol Signalling Studies, Freiburg, Germany
[3] Univ Freiburg, Fac Med, Berta Ottenstein Programme, Freiburg, Germany
关键词
CENTRAL-NERVOUS-SYSTEM; HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY; PERIVASCULAR MACROPHAGES; CHOROID-PLEXUS; MICROGLIAL CELLS; IMMUNOREGULATORY CELLS; IMMUNE PRIVILEGE; MANNOSE RECEPTOR; ADULT MICROGLIA; STEADY-STATE;
D O I
10.1038/ni.3703
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Myeloid cells in the central nervous system (CNS) represent a heterogeneous class of innate immune cells that contribute to the maintenance of tissue homeostasis differentially during development and adulthood. The subsets of CNS myeloid cells identified so far, including parenchymal microglia and non-parenchymal meningeal, perivascular and choroid-plexus macrophages, as well as disease-associated monocytes, have classically been distinguished on the basis of their surface epitope expression, localization and morphology. However, studies using cell-specific targeting, in vivo imaging, single-cell expression analysis and other sophisticated tools have now increased the depth of knowledge of this immune-cell compartment and call for reevaluation of the traditional views on the origin, fate and function of distinct CNS myeloid subsets. The concepts of CNS macrophage biology that are emerging from these new insights have broad implications for the understanding and treatment of CNS diseases.
引用
收藏
页码:385 / 392
页数:8
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