| Literature DB >> 36222957 |
Miao Chai1, Gang Su2, Juan Gao1, Wei Chen1, Qionghui Wu1, Ying Dong1, He Wang1, Deyi Chen1, Yonghong Li3, Xin Gao1, Ruixin Li1, Tianfei Ma1, Zhenchang Zhang4.
Abstract
Microglia, as innate immune cells in the brain, closely monitor changes in the internal environment and participate in the maintenance of homeostasis in the central nervous system (CNS). Microglia can be polarized to the M1 or M2 phenotype in response to various stimuli in vivo or in vitro, affecting the functions of peripheral neurons. M2 microglia have attracted increasing attention in recent years owing to their beneficial effects on various diseases and injuries of the CNS, such as traumatic brain injury, stroke, Alzheimer's disease and multiple sclerosis. They exert neuroprotective effects by various mechanisms, e.g., suppressing inflammation, promoting the degradation of misfolded and aggregated proteins, promoting neurite growth, enhancing neurogenesis, inhibiting autophagy and apoptosis, promoting myelination, maintaining blood-brain barrier integrity, and enhancing phagocytic activity.This review summarizes the molecular mechanisms by which M2 microglia exert protective effects on neurons and provides a reference for the selection of therapeutic targets for CNS diseases.Entities:
Keywords: CNS diseases; microglia polarization; neuroinflammation; neuroprotection
Year: 2022 PMID: 36222957 DOI: 10.1007/s11064-022-03760-4
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 4.414