Crosstalk between Microglia and Neurons in Neurotrauma: An Overview of the Underlying Mechanisms
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Bentham Science Publishers
Abstract
Microglia are the resident immune cells of the brain and play a crucial role in housekeep-ing 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 dis-rupt 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 recip-rocally communicate under physiological conditions and during brain injury and disease. Further-more, 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 fac-tors. In addition, it has been discussed that how microglia-neuron interactions could exert either beneficial neurotrophic effects or pathologic proinflammatory responses. We further explore how aberrations in microglia-neuron crosstalk may be involved in central nervous system (CNS) anoma-lies, 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. © 2022 Bentham Science Publishers.
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Cellular crosstalk, Cns injury, Microglia phenotypes, Microglia-neuron interaction, Microglial activation, Neuroinflammation, Brain, Brain injuries, Brain injuries, traumatic, Central nervous system diseases, Humans, Microglia, Neurons, Caspase recruitment domain protein 4, Cd163 antigen, Cd200 antigen, Cd200 receptor, Cd47 antigen, Cell surface protein, Chemokine receptor cx3cr1 antagonist, Cxcl9 chemokine, Fractalkine, Granulocyte macrophage colony stimulating factor, Interleukin 12, Interleukin 1beta, Interleukin 6, Monocyte chemotactic protein 1, Reactive oxygen metabolite, Secondary lymphoid tissue chemokine, Serotonin, Stromelysin, Toll like receptor, Tumor necrosis factor, Alzheimer disease, Bipolar disorder, Cell communication, Cell interaction, Disease exacerbation, Gene expression profiling, Human, Immune response, Ischemic stroke, Nerve cell network, Nerve cell plasticity, Nerve degeneration, Nervous system inflammation, Nervous system injury, Neuroprotection, Parkinson disease, Phenotype, Receptor cross-talk, Review, Schizophrenia, Traumatic brain injury, Brain injury, Central nervous system disease, Metabolism, Nerve cell, Pathology