Mechanisms of microglia-mediated synapse turnover and synaptogenesis

被引:12
|
作者
Ball, Jayson B. [1 ,2 ,3 ]
Green-Fulgham, Suzanne M. [1 ,2 ]
Watkins, Linda R. [1 ,2 ]
机构
[1] Univ Colorado, Dept Psychol & Neurosci, Boulder, CO 80309 USA
[2] Univ Colorado, Ctr Neurosci, Boulder, CO 80309 USA
[3] Univ Colorado Boulder, 2860 Wilderness Pl, Boulder, CO 80301 USA
来源
PROGRESS IN NEUROBIOLOGY | 2022年 / 218卷
关键词
Neuroplasticity; Dendritic spine; Microglia; Neuroimmune; Synapse; DENDRITIC SPINE STABILITY; NEUROTROPHIC FACTOR; MOLECULAR-MECHANISMS; NEGATIVE REGULATION; COMPLEMENT-SYSTEM; EXTRACELLULAR ATP; P2X RECEPTORS; CORD-INJURY; RAT-BRAIN; PHAGOCYTOSIS;
D O I
10.1016/j.pneurobio.2022.102336
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microglia shape synaptic connections among neurons of the central nervous system (CNS) during development and adulthood. In this review, the actions by which they facilitate pruning, refinement, and new synaptic development throughout the lifespan are considered, along with the molecular mechanisms by which neurons and microglia communicate to guide these actions. Microglia survey neuronal activity and selectively modify synaptic connections at the level of individual dendrites and synapses. This is important given that microglia are necessary for a healthy nervous system capable of learning and other neural phenomena based on synaptic modifications and can also cause pathological synaptic disfunctions in immunologically driven neurodegener-ative diseases. Understanding how microglia directly shape synaptic connections between neurons yields a more complete understanding of normal neuroplasticity and provides new routes for understanding disease states.
引用
收藏
页数:16
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