Key result
Apolipoprotein CIII knockout reduces aortic atherosclerosis lesion area by ~69% vs. wild-type.
Why the study?
High plasma apoCIII levels correlate with elevated triglycerides and increased cardiovascular risk, but whether apoCIII is directly involved in the development of atherosclerosis remains unclear.
Does apolipoprotein CIII deficiency prevent atherosclerosis in rabbits?
Does apolipoprotein CIII deficiency prevent atherosclerosis in rabbits?
Genetic deletion of apolipoprotein CIII accelerates triglyceride-rich lipoprotein clearance and robustly protects against diet-induced atherosclerosis in a rabbit model.
Answers are grounded in this paper and cite their sources.
ApoCIII knockout attenuates atherosclerosis in rabbits; leaves open human translation and therapeutic targeting.
OBJECTIVE: Apo (apolipoprotein) CIII mediates the metabolism of triglyceride (TG)-rich lipoproteins. High levels of plasma apoCIII are positively correlated with the plasma TG levels and increase the cardiovascular risk. However, whether apoCIII is directly involved in the development of atherosclerosis has not been fully elucidated. Approach and Results: To examine the possible roles of apoCIII in lipoprotein metabolism and atherosclerosis, we generated apoCIII KO (knockout) rabbits using ZFN (zinc finger nuclease) technique. On a normal standard diet, apoCIII KO rabbits exhibited significantly lower plasma levels of TG than those of WT (wild type) rabbits while total cholesterol and HDL (high-density lipoprotein) cholesterol levels were unchanged. Analysis of lipoproteins isolated by sequential ultracentrifugation revealed that reduced plasma TG levels in KO rabbits were accompanied by prominent reduction of VLDLs (very-low-density lipoproteins) and IDLs (intermediate-density lipoproteins). In addition, KO rabbits showed faster TG clearance rate after intravenous fat load than WT rabbits. On a cholesterol-rich diet, KO rabbits exhibited constantly and significantly lower levels of plasma total cholesterol and TG than WT rabbits, which was caused by a remarkable reduction of β-VLDLs-the major atherogenic lipoproteins. β-VLDLs of KO rabbits showed higher uptake by cultured hepatocytes and were cleared faster from the circulation than β-VLDLs isolated from WT rabbits. Both aortic and coronary atherosclerosis was significantly reduced in KO rabbits compared with WT rabbits. CONCLUSIONS: These results indicate that apoCIII deficiency facilitates TG-rich lipoprotein catabolism, and therapeutic inhibition of apoCIII expression may become a novel means not only for the treatment of hyperlipidemia but also for atherosclerosis.
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Yan et al. (2020) studied Atherosclerosis and hyperlipidemia. Apolipoprotein CIII gene knockout vs. Wild-type littermates was evaluated on Gross atherosclerotic lesion area of the whole aorta (69% reduction in homozygous knockout). Apolipoprotein CIII knockout significantly reduced gross aortic atherosclerosis lesion area by 69% and right coronary stenosis by 77% compared to wild-type rabbits on a cholesterol-rich diet.
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