| Literature DB >> 31062335 |
Chuan Qin1, Luo-Qi Zhou1, Xiao-Tong Ma1, Zi-Wei Hu1, Sheng Yang1, Man Chen1, Dale B Bosco2, Long-Jun Wu3, Dai-Shi Tian4.
Abstract
Ischemic stroke is a leading cause of morbidity and mortality worldwide. Resident microglia are the principal immune cells of the brain, and the first to respond to the pathophysiological changes induced by ischemic stroke. Traditionally, it has been thought that microglial activation is deleterious in ischemic stroke, and therapies to suppress it have been intensively explored. However, increasing evidence suggests that microglial activation is also critical for neurogenesis, angiogenesis, and synaptic remodeling, thereby promoting functional recovery after cerebral ischemia. Here, we comprehensively review the dual role of microglia during the different phases of ischemic stroke, and the possible mechanisms controlling the post-ischemic activity of microglia. In addition, we discuss the dynamic interactions between microglia and other cells, such as neurons, astrocytes, oligodendrocytes, and endothelial cells within the brain parenchyma and the neurovascular unit.Entities:
Keywords: Inflammation; Ischemic stroke; Microglia; Signaling pathways
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Year: 2019 PMID: 31062335 PMCID: PMC6754485 DOI: 10.1007/s12264-019-00388-3
Source DB: PubMed Journal: Neurosci Bull ISSN: 1995-8218 Impact factor: 5.203