Cellular prion protein acts as mediator of amyloid beta uptake by caveolin-1 causing cellular dysfunctions in vitro and in vivo

Alzheimers Dement. 2024 Oct;20(10):6776-6792. doi: 10.1002/alz.14120. Epub 2024 Aug 30.

Abstract

Introduction: Cellular prion protein (PrPC) was implicated in amyloid beta (Aβ)-induced toxicity in Alzheimer's disease (AD), but the precise molecular mechanisms involved in this process are unclear.

Methods: Double transgenic mice were generated by crossing Prnp knockout (KO) with 5xFAD mice, and light-sheet microscopy was used for whole brain tissue analyses. PrPC-overexpressing cells were developed for in vitro studies, and microscopy was used to assess co-localization of proteins of interest. Surface-plasmon resonance (SPR) was used to investigate protein-binding characteristics.

Results: In vivo, PrPC levels correlated with reduced lifespan and cognitive and motor function, and its ablation disconnected behavior deficits from Aβ levels. Light-sheet microscopy showed that PrPC influenced Aβ-plaque burden but not the distribution of those plaques. Interestingly, caveolin-1 (Cav-1) KO neurons significantly reduced intracellular Aβ-oligomer (Aβo) uptake when compared to wild-type neurons.

Discussion: The findings shed new light on the relevance of intracellular Aβo, suggesting that PrPC and Cav-1 modulate intracellular Aβ levels and the Aβ-plaque load.

Highlights: PrPC expression adversely affects lifespan and behavior in 5xFAD mice. PrPC increases Aβ1-40 and Aβ1-42 levels and Aβ-plaque load in 5xFAD mice. Cav-1 interacts with both PrPC and Aβ peptides. Knocking out Cav-1 leads to a significant reduction in intracellular Aβ levels.

Keywords: Alzheimer's disease; amyloid beta; caveolin; cellular prion protein.

MeSH terms

  • Alzheimer Disease* / genetics
  • Alzheimer Disease* / metabolism
  • Alzheimer Disease* / pathology
  • Amyloid beta-Peptides* / metabolism
  • Animals
  • Brain / metabolism
  • Caveolin 1* / genetics
  • Caveolin 1* / metabolism
  • Disease Models, Animal
  • Humans
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Neurons / metabolism
  • Plaque, Amyloid / metabolism
  • Plaque, Amyloid / pathology
  • PrPC Proteins / genetics
  • PrPC Proteins / metabolism
  • Prion Proteins* / genetics
  • Prion Proteins* / metabolism

Substances

  • Amyloid beta-Peptides
  • Caveolin 1
  • Prion Proteins
  • Prnp protein, mouse
  • PrPC Proteins