Cited by 3Alzheimer's disease research and treatmentsLipid metabolism and biosynthesisFerroptosis and cancer prognosis

APOE Genotype Impacts Polyunsaturated Neutral Lipid Storage and Ferroptosis Vulnerability in Astrocytes

Richards, Sarah E. V., Yang, Maddie, Deik, Amy A., Ricq, Emily L.·2025·Neurochemical Research

Abstract

Astrocytes play a critical role in regulating the metabolism of cholesterol and other lipids in the brain. Increasing evidence suggests that dysfunctional lipid metabolism and lipid peroxide-mediated cell death, or ferroptosis, are involved in the pathophysiology of late-onset Alzheimer’s disease. The Alzheimer’s disease risk allele of APOE, APOE4, is expressed in astrocytes and is associated with increased accumulation of cholesterol as well as highly polyunsaturated and peroxidation-prone neutral lipids in lipid droplets. However, a direct connection between APOE4 genotype-dependent lipid dysregulation and sensitivity to ferroptotic cell death has not yet been explored. Here, we show that APOE4 and APOE knockout astrocytes accumulate cholesterol and polyunsaturated lipid-rich droplets in lysosomes and have increased vulnerability to ferroptotic cell death. APOE2 astrocytes are also enriched in polyunsaturated lipids but are less vulnerable to lipid peroxidation. Pharmacological manipulation of neutral lipid content modestly impacted ferroptosis sensitivity. In contrast, modulation of lysosomal lipid content via blockade of autophagy or promotion of cholesterol efflux with methyl-β-cyclodextrin strongly protects APOE4 cells from lipid-peroxide mediated cell death. In humanized APOE4 mice, reduction of brain lipid peroxidation selectively impacted cholesterol ester storage. Taken together, these findings suggest that correction of APOE4-mediated lipid trafficking defects may reduce risk for ferroptotic in astrocytes.

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Crossref · 10.1007/s11064-025-04463-2

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Authors
Richards, S. E. V., Yang, M., Deik, A. A., & Ricq, E. L.
Affiliations
Broad Institute (US)
Corresponding author
Ricq, Emily L.
Venue
Neurochemical Research
Published
2025-06-26
Volume
50
Issue
4
Pages
211-211
ISSN
  • 0364-3190 (ISSN-L)
  • 1573-6903
OpenAlex
W4411673080
Cited by
3
References
54
Citations by year
2026: 3
FWCI
1.91
Type
journal article
Language
en
Open access
closed
Locations
  • Neurochemical Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute on Aging (R21 AG068769-01)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Ferroptosis and cancer prognosis
Keywords
APOE ε4, APOE2, astrocytes, ferroptosis, lipid peroxidation, lipid droplets, lysosomal lipid accumulation, autophagy, cholesterol efflux, methyl-β-cyclodextrin, late-onset Alzheimer's disease, lipid metabolism, ApoE-deficient mice
MeSH terms
Ferroptosis, Animals, Apolipoproteins E, Astrocytes, Cells, Cultured, Cholesterol, Genotype, Humans, Lysosomes, Lipid Peroxidation, Mice, Knockout, Lipid Metabolism, Mice, Apolipoprotein E4

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