A genetic variant of the Wnt receptor LRP6 accelerates synapse degeneration during aging and in Alzheimer's disease

Sci Adv. 2023 Jan 13;9(2):eabo7421. doi: 10.1126/sciadv.abo7421. Epub 2023 Jan 13.

Abstract

Synapse loss strongly correlates with cognitive decline in Alzheimer's disease (AD), but the underlying mechanisms are poorly understood. Deficient Wnt signaling contributes to synapse dysfunction and loss in AD. Consistently, a variant of the LRP6 receptor, (LRP6-Val), with reduced Wnt signaling, is linked to late-onset AD. However, the impact of LRP6-Val on the healthy and AD brain has not been examined. Knock-in mice, generated by gene editing, carrying this Lrp6 variant develop normally. However, neurons from Lrp6-val mice do not respond to Wnt7a, a ligand that promotes synaptic assembly through the Frizzled-5 receptor. Wnt7a stimulates the formation of the low-density lipoprotein receptor-related protein 6 (LRP6)-Frizzled-5 complex but not if LRP6-Val is present. Lrp6-val mice exhibit structural and functional synaptic defects that become pronounced with age. Lrp6-val mice present exacerbated synapse loss around plaques when crossed to the NL-G-F AD model. Our findings uncover a previously unidentified role for Lrp6-val in synapse vulnerability during aging and AD.

MeSH terms

  • Aging / genetics
  • Alzheimer Disease* / genetics
  • Alzheimer Disease* / metabolism
  • Animals
  • Low Density Lipoprotein Receptor-Related Protein-6* / genetics
  • Low Density Lipoprotein Receptor-Related Protein-6* / metabolism
  • Mice
  • Synapses / metabolism
  • Wnt Signaling Pathway

Substances

  • Low Density Lipoprotein Receptor-Related Protein-6
  • Lrp6 protein, mouse