Spatial heterogeneity in microglia-complement crosstalk: Implications for synaptic pruning in Alzheimer's disease

Alzheimers Dement. 2026 Feb;22(2):e71185. doi: 10.1002/alz.71185.

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by synaptic loss, as a key pathological feature in its early stages. Recent studies have highlighted the central role of microglia-complement interactions in synaptic pruning. This interaction exhibits significant spatial heterogeneity in AD, with activation patterns and functional manifestations varying across different brain regions and stages of disease. Therefore, this article systematically reviews the synergistic mechanisms of microglia and the complement system in physiological synaptic pruning. Additionally, the dynamic evolution of the complement-immune network during disease progression is analyzed, and the amplifying effect of genetic factors on the spatial heterogeneity of synaptic pruning is explored. Furthermore, current treatment strategies from both Western medicine and traditional Chinese medicine are discussed, emphasizing the potential value of combining these approaches for intervening in synaptic loss in AD.

Keywords: Alzheimer's disease; complement; microglia; spatial heterogeneity; synaptic pruning.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease* / immunology
  • Alzheimer Disease* / metabolism
  • Alzheimer Disease* / pathology
  • Animals
  • Brain* / immunology
  • Brain* / pathology
  • Complement System Proteins* / immunology
  • Complement System Proteins* / metabolism
  • Humans
  • Microglia* / immunology
  • Microglia* / metabolism
  • Neuronal Plasticity* / physiology
  • Synapses*

Substances

  • Complement System Proteins