Journal of Experimental Neuroscience

Synaptic plasticity critically depends on reciprocal interactions between neurons and glia. Among glial cells, microglia represent approximately 10% of the total brain cell population serve as the brain’s resident macrophage, and help to modulate neural activity. Because of their special role in the brain’s immune response, microglia are involved in the pathological progression of neurodegenerative disorders such as Alzheimer’s disease (AD). However, microglia also are surveyors of the brain’s health and continuously contact dendritic spines to regulate structural synaptic changes. This review summarizes our current understanding of neuronal-microglial signals that affect neural function at the synapse. Here, we examine the role of microglia in neuronal synapses in pathological brains and specifically focus on in vivo studies using 2-photon microscopy. Furthermore, because the role of microglia in AD progression is controversial, we outline the interaction between neurons and microglia in pathological conditions such as AD.