Microglia in Physiology and Disease

被引:1046
作者
Wolf, Susanne A. [1 ]
Boddeke, H. W. G. M. [2 ]
Kettenmann, Helmut [1 ]
机构
[1] Helmholtz Assoc, Max Delbruck Ctr Mol Med, Cellular Neurosci, D-13092 Berlin, Germany
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Neurosci, NL-9713 Groningen, Netherlands
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 79 | 2017年 / 79卷
关键词
pathology; synaptic pruning; phagocytosis; neurodegeneration; brain macrophages; immune responses; priming; aging; WILD-TYPE MICROGLIA; GENE-EXPRESSION; BIPOLAR DISORDER; BRAIN-DEVELOPMENT; CHRONIC STRESS; IMMUNE CELLS; NEUROINFLAMMATION; MACROPHAGE; GLIA; INFLAMMATION;
D O I
10.1146/annurev-physiol-022516-034406
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
As the immune-competent cells of the brain, microglia play an increasingly important role in maintaining normal brain function. They invade the brain early in development, transform into a highly ramified phenotype, and constantly screen their environment. Microglia are activated by any type of pathologic event or change in brain homeostasis. This activation process is highly diverse and depends on the context and type of the stressor or pathology. Microglia can strongly influence the pathologic outcome or response to a stressor due to the release of a plethora of substances, including cytokines, chemokines, and growth factors. They are the professional phagocytes of the brain and help orchestrate the immunological response by interacting with infiltrating immune cells. We describe here the diversity of microglia phenotypes and their responses in health, aging, and disease. We also review the current literature about the impact of lifestyle on microglia responses and discuss treatment options that modulate microglial phenotypes.
引用
收藏
页码:619 / 643
页数:25
相关论文
共 140 条
[1]  
Alzheimer A., 1910, HISTOLOGISCHE HISTOP, P401
[2]   The role of macrophage polarization on bipolar disorder: Identifying new therapeutic targets [J].
Ascoli, Bruna M. ;
Gea, Luiza P. ;
Colombo, Rafael ;
Barbe-Tuana, Florencia M. ;
Kapczinski, Flavio ;
Rosa, Adriane Ribeiro .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 2016, 50 (07) :618-630
[3]   Axon Initial Segment-Associated Microglia [J].
Baalman, Kelli ;
Marin, Miguel A. ;
Ho, Tammy Szu-Yu ;
Godoy, Marlesa ;
Cherian, Leela ;
Robertson, Claudia ;
Rasband, Matthew N. .
JOURNAL OF NEUROSCIENCE, 2015, 35 (05) :2283-2292
[4]   Characterization of Inflammatory Markers and Transcriptome Profiles of Differentially Activated Embryonic Stem Cell-Derived Microglia [J].
Beins, Eva ;
Ulas, Thomas ;
Ternes, Svenja ;
Neumann, Harald ;
Schultze, Joachim L. ;
Zimmer, Andreas .
GLIA, 2016, 64 (06) :1007-1020
[5]   The HPA - immune axis and the immunomodulatory actions of glucocorticoics in the brain [J].
Bellavance, Marc-Andre ;
Rivest, Serge .
FRONTIERS IN IMMUNOLOGY, 2014, 5
[6]   The role of microglia and myeloid immune cells in acute cerebral ischemia [J].
Benakis, Corinne ;
Garcia-Bonilla, Lidia ;
Iadecola, Costantino ;
Anrather, Josef .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2015, 8
[7]   What is microglia neurotoxicity (Not)? [J].
Biber, Knut ;
Owens, Trevor ;
Boddeke, Erik .
GLIA, 2014, 62 (06) :841-854
[8]   Microglia function during brain development: New insights from animal models [J].
Bilimoria, Parizad M. ;
Stevens, Beth .
BRAIN RESEARCH, 2015, 1617 :7-17
[9]   DISPLACEMENT OF SYNAPTIC TERMINALS FROM REGENERATING MOTONEURONS BY MICROGLIAL CELLS [J].
BLINZING.K ;
KREUTZBE.G .
ZEITSCHRIFT FUR ZELLFORSCHUNG UND MIKROSKOPISCHE ANATOMIE, 1968, 85 (02) :145-&
[10]   Macrophage subsets and microglia in multiple sclerosis [J].
Bogie, Jeroen F. J. ;
Stinissen, Piet ;
Hendriks, Jerome J. A. .
ACTA NEUROPATHOLOGICA, 2014, 128 (02) :191-213