Cited by 423Cholesterol and Lipid MetabolismSteroid Chemistry and BiochemistryPharmacogenetics and Drug Metabolism

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

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Abstract

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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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
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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