Open AccessThe Role of Complement in Synaptic Pruning and Neurodegeneration
Author(s) -
Ángela Gómez-Arboledas,
Munjal M. Acharya,
Andrea J. Tenner
Publication year - 2021
Publication title -
immunotargets and therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.256
H-Index - 7
ISSN - 2253-1556
DOI - 10.2147/itt.s305420
Subject(s) - synaptic pruning , neurodegeneration , neuroscience , complement system , synaptic plasticity , multiple sclerosis , complement (music) , innate immune system , disease , immune system , biology , medicine , inflammation , microglia , immunology , phenotype , pathology , receptor , biochemistry , complementation , gene
The complement system, an essential part of the innate immune system, is composed of a group of secreted and membrane proteins that collectively participate in maintaining the function of the healthy and diseased brain. However, an inappropriate activation of the complement system has been related to an inflammatory response in multiple diseases, such as stroke, traumatic brain injury, multiple sclerosis, and Alzheimer's disease, as well as Zika infection and radiotherapy. In addition, C1q and C3 (initial activation components of the complement cascade) have been shown to play a key beneficial role in the refinement of synaptic circuits during developmental stages and adult plasticity. Nevertheless, excessive synaptic pruning in the adult brain can be detrimental and has been associated with synaptic loss in several pathological conditions. In this brief review, we will discuss the role of the complement system in synaptic pruning as well as its contribution to neurodegeneration and cognitive deficits. We also mention potential therapeutic approaches to target the complement system to treat several neuroinflammatory diseases and unintended consequences of radiotherapy.