Abstract
Scavenger receptor BI (SR-BI) is a multi-functional receptor that plays an essential role in reverse cholesterol transport (RCT) and prevention of atherosclerotic lesion development. It mediates the selective uptake of cholesteryl esters from high-density lipoprotein (HDL) by the liver, the final step in the RCT pathway. In addition, it has been implicated in binding and uptake of native apolipoprotein B (apoB) containing lipoproteins and the bi-directional transport of cholesterol between cells and HDL. Recent studies have also indicated that SR-BI is essential for adrenal steroidogenesis by facilitating the uptake of cholesterol from HDL by the adrenal and that deletion of SR-BI leads to an increased susceptibility to arterial thrombosis and an altered platelet response.
Most studies on SR-BI have been performed in mice and for long it was questioned whether SR-BI was also important for cholesterol metabolism in humans. Recently, however, heterozygote carriers of a functional P297S mutation in the SR-BI gene were identified in the Netherlands in whom it for the first time could be demonstrated that also in humans SR-BI is essential for HDL metabolism, adrenal glucocorticoid output, and platelet function.
In conclusion, SR-BI is a multi-purpose player in cholesterol and steroid metabolism in mice and man that might have potential as a therapeutic target for treatment of atherosclerosis and atherothrombosis.
Original language | English |
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Title of host publication | Atherosclerosis |
Subtitle of host publication | Risks, Mechanisms, and Therapies |
Editors | Hong Wang, Cam Patterson |
Publisher | Wiley |
Pages | 313-328 |
ISBN (Electronic) | 9781118828533 |
ISBN (Print) | 1118285913, 978-1-118-28591-6 |
DOIs | |
Publication status | Published - 1 May 2015 |
Keywords
- high density lipoprotein (HDL) metabolism
- lipid homeostasis
- macrophages
- multipurpose player
- scavenger receptor class B type I
- SR-BI knockout (KO) mice