PreprintCited by 0Mitochondrial Function and PathologyAlzheimer's disease research and treatmentsATP Synthase and ATPases Research

Elevated cholesterol in APOE4 astrocytes drives mitochondrial cristae collapse and ATP synthase dysfunction

Lee, Seungtae, Munoz-Oreja, Mikel, Villar-Fernandez, Marina, Goicoechea-Barrenechea, Leire, Fernandez-Pelayo, Uxoa, Perez-Rodriguez, Diego, Gegg, Matthew, de Arbina, Amaia Lopez +2 more·2026·bioRxiv (Cold Spring Harbor Laboratory)

Abstract

Cholesterol imbalance is a hallmark of major human diseases, including atherosclerosis and Alzheimer’s disease, both of which are also associated with mitochondrial dysfunction, yet the mechanistic links between cholesterol and mitochondria remain poorly understood. Here we show that elevated intracellular cholesterol in murine astrocytes expressing the Alzheimer’s disease risk variant APOE4 disrupts the inner mitochondrial membrane, manifesting as sparse, truncated cristae alongside an excess of cristae junction complexes. These structural abnormalities are accompanied by loss of respiratory chain complexes I and IV, and reduced respiration; nevertheless, low proton leak and reverse ATP synthase activity combine to generate an elevated mitochondrial membrane potential. Strikingly, APOE4 astrocytes are hypersensitive to the ATP synthase inhibitor oligomycin, demonstrating a profound dysfunction of the enzyme, and cholesterol sequestration with methyl-β-cyclodextrin abrogates this toxicity, establishing elevated cholesterol as its proximate cause. Another method of targeting ATP synthase, epicatechin, which prevents the enzyme operating in reverse, attenuated both cholesterol- and respiratory chain inhibitor-induced cell death. Reciprocally, reducing intracellular cholesterol via nutrient restriction restored cristae architecture and partially rescued respiratory chain complex abundance. These findings identify mitochondrial cholesterol as a critical determinant of cristae architecture and ATP synthase function and suggest that cholesterol-driven mitochondrial dysfunction may be a unifying feature of cholesterol-related disorders from neurodegeneration to atherosclerosis. GRAPHICAL ABSTRACT: Elevated intracellular cholesterol in APOE4 astrocytes disrupts the inner mitochondrial membrane and ATP synthase, resulting in sparse cristae, increased ATP hydrolysis and heightened oligomycin sensitivity. The vulnerability to oligomycin is abrogated by cholesterol sequestration with cyclodextrin, indicating causality. These findings position cholesterol as a key determinant of the cristae landscape and ATP synthase function, highlighting the importance of the emerging field of mitochondrial-cholesterol crosstalk.

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Crossref · 10.64898/2026.08.04.742391

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  1. 1992, Low mitochondrial proton leak due to high membrane cholesterol content and cytosolic creatine kinase as two features of the deviant bioenergetics of Ehrlich and AS30-D tumor cells, Cancer Research, 52, 4935

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Authors
Lee, S., Munoz-Oreja, M., Villar-Fernandez, M., Goicoechea-Barrenechea, L., Fernandez-Pelayo, U., Perez-Rodriguez, D., Gegg, M., de Arbina, A. L., Spinazzola, A., & Holt, I. J.
Affiliations
  • Biogipuzkoa Health Research Institute (ES)
  • Biogipuzkoa Health Research Institute, 20014, San Sebastián, Spain
  • Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, Royal Free Campus, London NW3 2PF, UK
  • The Royal Free Hospital (GB)
  • Ikerbasque (ES)
Corresponding author
Holt, Ian James
Venue
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Published
2026-08-04
OpenAlex
W7172494689
Cited by
0
References
44
Type
posted content
Language
en
Open access
closed
Locations
bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › ATP Synthase and ATPases Research
Keywords
intracellular cholesterol, APOE ε4, astrocytes, mitochondrial cristae, mitochondrial dysfunction, oligomycin sensitivity, mitochondrial membrane potential, respiratory chain complexes, epicatechin, methyl-β-cyclodextrin, Alzheimer's disease, atherosclerosis, nutrient restriction

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