APOE4 to APOE2 allelic switching in mice improves Alzheimer’s disease-related metabolic signatures, neuropathology and cognition

Compared to individuals carrying two copies of the ε4 allele of apolipoprotein E (APOE), ε2 homozygotes have an approximate 99% reduction in late-onset Alzheimer's disease (AD) risk. Here we develop a knock-in model that allows for an inducible 'switch' between risk and protective alleles (APOE4s2). Gene expression and proteomic analyses confirm that APOE4s2 mice synthesize E4 at baseline and E2 after tamoxifen administration. A whole-body allelic switch results in a metabolic profile resembling E2/E2 humans and drives AD-relevant alterations in the lipidome and single-cell transcriptome, particularly in astrocytes. Finally, when crossed to the 5xFAD background, astrocyte-specific E4 to E2 switching improves cognition, decreases amyloid pathology, lowers gliosis and reduces plaque-associated apolipoprotein E. Together, these data show that a short-term transition from APOE4 to APOE2 can broadly affect the cerebral transcriptome and lipidome, and that astrocyte-specific APOE replacement may be a viable strategy for future gene editing approaches to simultaneously reduce multiple AD-associated pathologies.

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Publication Details

Journal
Nature Neuroscience
Published
2025-11-11
DOI
https://doi.org/10.1038/s41593-025-02094-y
Citations
6
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
6.99
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article

APOE4 to APOE2 allelic switching in mice improves Alzheimer’s disease-related metabolic signatures, neuropathology and cognition

Cathryn T Smith, Kai Saito, Brandon C. Farmer, Lance A. Johnson et al.
6 citations
Nature Neuroscience
Alzheimer's disease research and treatments
6.99
article

APOE4 to APOE2 allelic switching in mice improves Alzheimer’s disease-related metabolic signatures, neuropathology and cognition

Cathryn T Smith, Kai Saito, Brandon C. Farmer, Lance A. Johnson, Kumar Pandya, Lesley R. Golden, Dale O. Cowley, Callie M Whitus, Scott M. Gordon, Jessica L. Funnell, Josh M. Morganti, Shannon L. Macauley, Sangderk Lee, Haining Zhu, Steven M. MacLean, Gabriela Hernandez, Georgia L. Nolt, Jing Chen, Clairity Voy, Isaiah O. Stephens, Dahlia Siano, Akhil V. Pallerla
article en
6 citations

Abstract

Compared to individuals carrying two copies of the ε4 allele of apolipoprotein E (APOE), ε2 homozygotes have an approximate 99% reduction in late-onset Alzheimer's disease (AD) risk. Here we develop a knock-in model that allows for an inducible 'switch' between risk and protective alleles (APOE4s2). Gene expression and proteomic analyses confirm that APOE4s2 mice synthesize E4 at baseline and E2 after tamoxifen administration. A whole-body allelic switch results in a metabolic profile resembling E2/E2 humans and drives AD-relevant alterations in the lipidome and single-cell transcriptome, particularly in astrocytes. Finally, when crossed to the 5xFAD background, astrocyte-specific E4 to E2 switching improves cognition, decreases amyloid pathology, lowers gliosis and reduces plaque-associated apolipoprotein E. Together, these data show that a short-term transition from APOE4 to APOE2 can broadly affect the cerebral transcriptome and lipidome, and that astrocyte-specific APOE replacement may be a viable strategy for future gene editing approaches to simultaneously reduce multiple AD-associated pathologies.

Nature NeuroscienceVol. 28(12)
University of North Carolina at Chapel Hill (US), University of Arizona (US), University of Kentucky (US), Transgenomic (United States) (US)
Openalex Percentile: Top 3%
Alzheimer's disease research and treatments
6.99
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