2013Neural PlasticityOpen access

Microglia in Neuronal Circuits

Long‐Jun Wu, Beth Stevens, Shumin Duan, Brian A. MacVicar

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Abstract

Microglia comprise a unique subset of glial cells as the principal brain immune cells and are actively engaged in physiological and pathological brain functions. Unlike other resident neural cells that are of neuroectodermal origin, microglia are of mesodermal origin and invade the neuroepithelium at early embryonic stages. As resident immune response cells, microglia are extremely sensitive to almost any brain disturbance. Therefore, microglia are traditionally recognized for their immune functions during acute brain injury, such as bacterial meningitis, ischemic stroke, and spinal cord injury, as well as chronic neurological disorders, such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, and neuropathic pain. Recently, the role of microglia in neurodevelopment and neural plasticity in the healthy brains has gained tremendous attention. These exciting results raise an intriguing possibility that microglia can integrate into the neuronal circuits in the healthy and diseased brain. In support of this notion, it is emerging that microglia have remarkably dynamic processes and are frequently interacting with neurons and synaptic elements. Through these interactions, microglia may monitor neuronal/synaptic activities and thus survey the microenvironment in the brain. Indeed, recent studies have apparently shown that microglia function in neuronal circuits by playing diverse roles in neural development, behavior, and pathology in the brain. Therefore, microglia research has changed the way we think about neuronal network/plasticity and increased our understanding of brain diseases associated with abnormal microglia. Contributions to this special issue provide a snapshot of microglial function in the healthy and diseased brain and propose a fundamental role of microglia in neuronal circuits.

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Microglia comprise a unique subset of glial cells as the principal brain immune cells and are actively engaged in physiological and pathological brain functions. Unlike other resident neural cells that are of neuroectodermal origin, microglia are of mesodermal origin and invade the neuroepithelium at early embryonic stages. As resident immune response cells, microglia are extremely sensitive to almost any brain disturbance. Therefore, microglia are traditionally recognized for their immune functions during acute brain injury, such as bacterial meningitis, ischemic stroke, and spinal cord injury, as well as chronic neurological disorders, such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, and neuropathic pain. Recently, the role of microglia in neurodevelopment and neural plasticity in the healthy brains has gained tremendous attention. These exciting results raise an intriguing possibility that microglia can integrate into the neuronal circuits in the healthy and diseased brain. In support of this notion, it is emerging that microglia have remarkably dynamic processes and are frequently interacting with neurons and synaptic elements. Through these interactions, microglia may monitor neuronal/synaptic activities and thus survey the microenvironment in the brain. Indeed, recent studies have apparently shown that microglia function in neuronal circuits by playing diverse roles in neural development, behavior, and pathology in the brain. Therefore, microglia research has changed the way we think about neuronal network/plasticity and increased our understanding of brain diseases associated with abnormal microglia. Contributions to this special issue provide a snapshot of microglial function in the healthy and diseased brain and propose a fundamental role of microglia in neuronal circuits.

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Available abstract

Microglia comprise a unique subset of glial cells as the principal brain immune cells and are actively engaged in physiological and pathological brain functions. Unlike other resident neural cells that are of neuroectodermal origin, microglia are of mesodermal origin and invade the neuroepithelium at early embryonic stages. As resident immune response cells, microglia are extremely sensitive to almost any brain disturbance. Therefore, microglia are traditionally recognized for their immune functions during acute brain injury, such as bacterial meningitis, ischemic stroke, and spinal cord injury, as well as chronic neurological disorders, such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, and neuropathic pain. Recently, the role of microglia in neurodevelopment and neural plasticity in the healthy brains has gained tremendous attention. These exciting results raise an intriguing possibility that microglia can integrate into the neuronal circuits in the healthy and diseased brain. In support of this notion, it is emerging that microglia have remarkably dynamic processes and are frequently interacting with neurons and synaptic elements. Through these interactions, microglia may monitor neuronal/synaptic activities and thus survey the microenvironment in the brain. Indeed, recent studies have apparently shown that microglia function in neuronal circuits by playing diverse roles in neural development, behavior, and pathology in the brain. Therefore, microglia research has changed the way we think about neuronal network/plasticity and increased our understanding of brain diseases associated with abnormal microglia. Contributions to this special issue provide a snapshot of microglial function in the healthy and diseased brain and propose a fundamental role of microglia in neuronal circuits.

Key concepts: Microglia, Neuroscience, Biological neural network, Neuroplasticity, Biology, Multiple sclerosis, Immune system, Inflammation

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