A Lipid-Raft Theory of Alzheimer's Disease

Ari Rappoport*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

2 Scopus citations

Abstract

I present a theory of Alzheimer’s disease (AD) that explains its symptoms, pathology, and risk factors. To do this, I introduce a new theory of brain plasticity that elucidates the physiological roles of AD-related agents. New events generate synaptic and branching candidates competing for long-term enhancement. Competition resolution crucially depends on the formation of membrane lipid rafts, which requires astrocyte-produced cholesterol. Sporadic AD is caused by impaired formation of plasma-membrane lipid rafts, preventing the conversion of short- to long-term memory and yielding excessive tau phosphorylation, intracellular cholesterol accumulation, synaptic dysfunction, and neurodegeneration. Amyloid β (Aβ) production is promoted by cholesterol during the switch to competition resolution, and cholesterol accumulation stimulates chronic Aβ production, secretion, and aggregation. The theory addresses all of the major established facts known about the disease and is supported by strong evidence.

Original languageEnglish
Pages (from-to)387-416
Number of pages30
JournalAnnual Review of Biochemistry
Volume94
Issue number1
DOIs
StatePublished - 20 Jun 2025

Bibliographical note

Publisher Copyright:
© 2025 by the author(s).

Keywords

  • adaptive response plasticity
  • Alzheimer’s disease
  • cholesterol
  • double-edged plasticity
  • lipid rafts
  • short-term memory

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