小胶质细胞
神经科学
神经炎症
串扰
神经保护
神经退行性变
创伤性脑损伤
神经营养因子
神经元
医学
中枢神经系统
生物
作者
Muhammad Ali Haidar,Stanley Ibeh,Zaynab Shakkour,Mohammad Amine Reslan,Judith Nwaiwu,Yomna Adel Moqidem,Georgio Sader,Rachel G Nickles,Ismail Babale,Aneese A Jaffa,Mohamed Salama,Abdullah Shaito,Firas Kobeissy
标识
DOI:10.2174/1570159x19666211202123322
摘要
Microglia are the resident immune cells of the brain and play a crucial role in housekeeping and maintaining homeostasis of the brain microenvironment. Upon injury or disease, microglial cells become activated, at least partly, via signals initiated by injured neurons. Activated microglia, thereby, contribute to both neuroprotection and neuroinflammation. However, sustained microglial activation initiates a chronic neuroinflammatory response which can disturb neuronal health and disrupt communications between neurons and microglia. Thus, microglia-neuron crosstalk is critical in a healthy brain as well as during states of injury or disease. As most studies focus on how neurons and microglia act in isolation during neurotrauma, there is a need to understand the interplay between these cells in brain pathophysiology. This review highlights how neurons and microglia reciprocally communicate under physiological conditions and during brain injury and disease. Furthermore, the modes of microglia-neuron communication are exposed, focusing on cell-contact dependent signaling and communication by the secretion of soluble factors like cytokines and growth factors. In addition, how microglia-neuron interactions could exert either beneficial neurotrophic effects or pathologic proinflammatory responses are discussed. We further explore how aberrations in microglia-neuron crosstalk may be involved in central nervous system (CNS) anomalies, namely: traumatic brain injury (TBI), neurodegeneration, and ischemic stroke. A clear understanding of how the microglia-neuron crosstalk contributes to the pathogenesis of brain pathologies may offer novel therapeutic avenues of brain trauma treatment.
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