The DOI matches its Crossref record; 53 of the 55 references it cites were found in a registry or an index.
Knockout of the Cholesterol 24-Hydroxylase Gene in Mice Reveals a Brain-specific Mechanism of Cholesterol Turnover
Open accessAbstract
Most cholesterol turnover takes place in the liver and involves the conversion of cholesterol into soluble and readily excreted bile acids. The synthesis of bile acids is limited to the liver, but several enzymes in the bile acid biosynthetic pathway are expressed in extra-hepatic tissues and there also may contribute to cholesterol turnover. An example of the latter type of enzyme is cholesterol 24-hydroxylase, a cytochrome P450 (CYP46A1) that is expressed at 100-fold higher levels in the brain than in the liver. Cholesterol 24-hydroxylase catalyzes the synthesis of the oxysterol 24(S)-hydroxycholesterol. To assess the relative contribution of the 24-hydroxylation pathway to cholesterol turnover, we performed balance studies in mice lacking the cholesterol 24-hydroxylase gene (Cyp46a1-/- mice). Parameters of hepatic cholesterol and bile acid metabolism in the mutant mice remained unchanged relative to wild type controls. In contrast to the liver, the synthesis of new cholesterol was reduced by approximately 40% in the brain, despite steady-state levels of cholesterol being similar in the knockout mice. These data suggest that the synthesis of new cholesterol and the secretion of 24(S)-hydroxycholesterol are closely coupled and that at least 40% of cholesterol turnover in the brain is dependent on the action of cholesterol 24-hydroxylase. We conclude that cholesterol 24-hydroxylase constitutes a major tissue-specific pathway for cholesterol turnover in the brain.
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“To maintain homeostasis, cholesterol can be converted into the oxysterol 24(S)-hydroxycholesterol (24S-OHC) by the neuron-specific enzyme CYP46A1 (figure 4a) [162].”
From Rett syndrome: a neurological disorder with metabolic components (2018) · cites this paper as [162]
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“The only other mouse mutant to show decreased brain cholesterol synthesis is Cyp46a1, which lacks 24SOHC, required for brain cholesterol turnover44.”
From A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome (2013) · cites this paper as [44]
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Self-citationVisualizing an Olfactory Sensory Map
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Cellular cholesterol trafficking and compartmentalization
Ikonen, E. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2336 · Cited by 1,506
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Self-citationBrain Cholesterol: Long Secret Life Behind a Barrier
Björkhem, I., & Meaney, S. (2004) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.0000120374.59826.1b · Cited by 1,044
Cholesterol metabolism and homeostasis in the brain
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Cholesterol Sensing, Trafficking, and Esterification
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Metadata
- Authors
- Lund, E. G., Xie, C., Kotti, T., Turley, S. D., Dietschy, J. M., & Russell, D. W.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Corresponding author
- Russell, David W.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2003-06
- Volume
- 278
- Issue
- 25
- Pages
- 22980-22988
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2002793897
- Cited by
- 421
- References
- 55
- Citations by year
- 2026: 10 · 2025: 21 · 2024: 14 · 2023: 27 · 2022: 28 · 2021: 29 · 2020: 21 · 2019: 20 · 2018: 18 · 2017: 11 · 2016: 18 · 2015: 17 · 2014: 17 · 2013: 21 · 2012: 15
- FWCI
- 15.38
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (R37-HL 09610, R37HL009610, P01 HL-20948, P01HL020948)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
- Physical Sciences › Chemistry › Organic Chemistry › Steroid Chemistry and Biochemistry
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Keywords
- cholesterol 24-hydroxylase, CYP46A1, 24S-hydroxycholesterol, oxysterols, bile acid synthesis, hepatic cholesterol metabolism, knockout mice
- MeSH terms
- Cholesterol 24-Hydroxylase, Alleles, Animals, beta-Galactosidase, Brain, Cholesterol, Cholesterol, Dietary, Embryonic and Fetal Development, Kinetics, Liver, RNA, Messenger, Steroid Hydroxylases, Transcription, Genetic, Restriction Mapping, Gene Expression Regulation, Enzymologic, Mice, Knockout, Gene Expression Regulation, Developmental, Mice
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