期刊
NEUROCHEMISTRY INTERNATIONAL
卷 143, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2020.104943
关键词
Microglia; Stress; Noradrenaline; Locus coeruleus; Adrenergic receptor; Neuroinflammation
资金
- Ministry of Education, Culture, Sports, Science and Technology of Japan
The state of mind can influence susceptibility and progression of diseases in the central nervous system, with noradrenaline playing crucial roles in modulating microglial cells. Microglial cells under different conditions may have constructive or detrimental roles in surveillance activities, affecting brain waste clearance. This review discusses the underlying mechanism and roles of stress-induced microglial activation.
State of mind can influence susceptibility and progression of diseases and disorders not only in peripheral organs, but also in the central nervous system (CNS). However, the underlying mechanism how state of mind can affect susceptibility to various illnesses in the CNS is not fully understood. Among a number of candidates responsible for stress-induced neuroimmunomodulation, noradrenaline has recently been shown to play crucial roles in the major immune cells of the brain, microglia. In particular, recent studies have demonstrated that noradrenaline may be a key neurotransmitter in modulating microglial cells, thereby determining different cell conditions and responses ranging from resting to activation state depending on host stress level or whether the host is awake or asleep. For instance, microglia under resting conditions may have constructive roles in surveillance, such as debris clearance, synaptic monitoring, pruning, and remodeling. In contrast, once activated, microglia may become less efficient in surveillance activities, and instead implicated in detrimental roles such as cytokine or superoxide release. It is also likely that glial activation, both astrocytes and microglia, are negatively associated with the clearance of brain waste via the glymphatic system. In this review, we discuss the possible underlying mechanism as well as the roles of stress-induced microglial activation.
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