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Genetic Variant of the Scavenger Receptor BI in Humans
Open accessAbstract
BACKGROUND: In mice, the scavenger receptor class B type I (SR-BI) is essential for the delivery of high-density lipoprotein (HDL) cholesterol to the liver and steroidogenic organs. Paradoxically, elevated HDL cholesterol levels are associated with increased atherosclerosis in SR-BI-knockout mice. It is unclear what role SR-BI plays in human metabolism. METHODS: We sequenced the gene encoding SR-BI in persons with elevated HDL cholesterol levels and identified a family with a new missense mutation (P297S). The functional effects of the P297S mutation on HDL binding, cellular cholesterol uptake and efflux, atherosclerosis, platelet function, and adrenal function were studied. RESULTS: Cholesterol uptake from HDL by primary murine hepatocytes that expressed mutant SR-BI was reduced to half of that of hepatocytes expressing wild-type SR-BI. Carriers of the P297S mutation had increased HDL cholesterol levels (70.4 mg per deciliter [1.8 mmol per liter], vs. 53.4 mg per deciliter [1.4 mmol per liter] in noncarriers; P<0.001) and a reduced capacity for efflux of cholesterol from macrophages, but the carotid artery intima-media thickness was similar in carriers and in family noncarriers. Platelets from carriers had increased unesterified cholesterol content and impaired function. In carriers, adrenal steroidogenesis was attenuated, as evidenced by decreased urinary excretion of sterol metabolites, a decreased response to corticotropin stimulation, and symptoms of diminished adrenal function. CONCLUSIONS: We identified a family with a functional mutation in SR-BI. The mutation carriers had increased HDL cholesterol levels and a reduction in cholesterol efflux from macrophages but no significant increase in atherosclerosis. Reduced SR-BI function was associated with altered platelet function and decreased adrenal steroidogenesis. (Funded by the European Community and others.).
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“common genetic variants near SCARB1 have been found to be correlated with plasma HDL-C levels (57, 58)”
From The hepatic WASH complex is required for efficient plasma LDL and HDL cholesterol clearance (2019) · cites this paper as [58]
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“Only recently, mutations of scavenger receptor (SR-BI) (P279S, P376L) have been described which are associated with both significant increases in HDL-C and increased cardiovascular risk [38–40].”
From HDL cholesterol: reappraisal of its clinical relevance (2017) · cites this paper as [38]
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Yang, X., Sethi, A. A., Yanek, L. R., Knapper, C., Nordestgaard, B. G., Tybjærg‐Hansen, A., Becker, D. M., Mathias, R. A., Remaley, A. T., & Becker, L. C. (2016) · Circulation Cardiovascular Genetics · doi:10.1161/circgenetics.116.001402 · Cited by 39
Wang, W., Chen, K., Su, Y., Zhang, J., Li, M., & Zhou, J. (2018) · Biomacromolecules · doi:10.1021/acs.biomac.7b01549 · Cited by 38
SR-B1’s Next Top Model: Structural Perspectives on the Functions of the HDL Receptor
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Cardiac and skeletal muscles show molecularly distinct responses to cancer cachexia
Shum, A. M. Y., Fung, D. C. Y., Corley, S., McGill, M. C., Bentley, N. L., Tan, T. C., Wilkins, M. R., & Polly, P. (2015) · Physiological Genomics · doi:10.1152/physiolgenomics.00128.2014 · Cited by 38
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Familial hypercholesterolaemia: cholesterol efflux and coronary disease
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Functional validation of new pathways in lipoprotein metabolism identified by human genetics
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New developments in selective cholesteryl ester uptake
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Pinto, P. R., Rocco, D. D. F. M., Okuda, L. S., Machado‐Lima, A., Castilho, G., da Silva, K. S., Gomes, D. J., Pinto, R. D. S., Iborra, R. T., Ferreira, G. S., et al. (2015) · Lipids in Health and Disease · doi:10.1186/s12944-015-0093-3 · Cited by 35
Okada, T., Ohama, T., Takafuji, K., Kanno, K., Matsuda, H., Sairyo, M., Zhu, Y., Saga, A., Kobayashi, T., Masuda, D., et al. (2019) · Journal of clinical lipidology · doi:10.1016/j.jacl.2019.01.002 · Cited by 33
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Developmental abnormalities in mouse embryos lacking the HDL receptor SR-BI
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Metadata
- Authors
- Vergeer, M., Korporaal, S. J. A., Franssen, R., Meurs, I., Out, R., Hovingh, G. K., Hoekstra, M., Sierts, J. A., Dallinga-Thie, G. M., Motazacker, M. M., Holleboom, A. G., Van Berkel, T. J. C., Kastelein, J. J. P., Van Eck, M., & Kuivenhoven, J. A.
- Affiliations
- Amsterdam UMC Location University of Amsterdam (NL)
- Leiden University (NL)
- ORCID
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2011-01-13
- Volume
- 364
- Issue
- 2
- Pages
- 136-145
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2077942032
- Cited by
- 317
- References
- 40
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 7 · 2023: 7 · 2022: 18 · 2021: 17 · 2020: 14 · 2019: 19 · 2018: 17 · 2017: 29 · 2016: 14 · 2015: 29 · 2014: 34 · 2013: 34 · 2012: 31
- FWCI
- 42.84
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Keywords
- scavenger receptor class B type I, HDL cholesterol, high HDL cholesterol, cholesterol absorption, HDL binding, macrophage cholesterol efflux, atherosclerosis, platelet function, adrenal steroidogenesis, familial hypercholesterolemia
- MeSH terms
- Adolescent, Adrenal Insufficiency, Adrenal Glands, Adult, Aged, Aged, 80 and over, Animals, Carotid Arteries, Cholesterol, DNA Mutational Analysis, Female, Heterozygote, Homeostasis, Humans, Hydrocortisone, Cholesterol, HDL, Macrophages, Male, Middle Aged, Pedigree, Triglycerides, Platelet Activation, Mice, Knockout, Mutation, Missense, Atherosclerosis, Scavenger Receptors, Class B, Mice, Young Adult
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