AI Article Synopsis

  • The immune system, particularly microglia (the brain's immune cells), may be crucial in the early stages of Alzheimer's disease, despite the unknown cause.
  • Genome-wide studies have linked various genes associated with Alzheimer's to immune cell dysfunction, indicating a significant role in the disease's development.
  • Microglia not only clear harmful proteins like amyloid-β but also support neurons and regulate synaptic activity, suggesting their dysfunction could contribute to early network abnormalities in Alzheimer's.

Article Abstract

Although the cause of Alzheimer's disease (AD) remains unknown, a number of new findings suggest that the immune system may play a critical role in the early stages of the disease. Genome-wide association studies have identified a wide array of risk-associated genes for AD, many of which are associated with abnormal functioning of immune cells. Microglia are the brain's immune cells. They play an important role in maintaining the brain's extracellular environment, including clearance of aggregated proteins such as amyloid-β (Aβ). Recent studies suggest that microglia play a more active role in the brain than initially considered. Specifically, microglia provide trophic support to neurons and also regulate synapses. Microglial regulation of neuronal activity may have important consequences for AD. In this article we review the function of microglia in AD and examine the possible relationship between microglial dysfunction and network abnormalities, which occur very early in disease pathogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927862PMC
http://dx.doi.org/10.3233/JAD-151075DOI Listing

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