Key result
APOA5 knockout cuts protein ~90%, driving dyslipidemia and severe atherosclerosis in rabbits.
Why the study?
No rabbit APOA5 loss-of-function model has previously been described despite the importance of APOA5 in regulating plasma triglycerides and limitations of murine models.
Biallelic disruption of APOA5 in rabbits creates a translationally relevant model of human APOA5 deficiency for testing triglyceride-lowering therapies and studying residual cardiovascular risk.
Rabbit APOA5 knockout model may accelerate dyslipidemia research; leaves open translation to human therapies.
ApolipoproteinA5 (APOA5) plays an important role in regulating plasma triglycerides (TG). Most in vivo data, however, derive from murine models whose lipoprotein metabolism diverges substantially from humans, and no rabbit APOA5 loss-of-function model has previously been described. Microinjection of Cas9 mRNA and two exon-2-targeting sgRNAs into rabbit zygotes yielded 10 founders carrying biallelic loss-of-function alleles, and with an approximately 90% reduction in plasma APOA5 protein. On chow, APOA5 mutant rabbits developed a stable atherogenic dyslipidemia with selectively elevated plasma triglycerides and reduced HDL-cholesterol, both more severe in male than in female mutants. The dyslipidemia was paralleled by accumulation of apolipoprotein B-containing lipoproteins, an enlarged VLDL distribution by fast-protein liquid chromatography, and reduced pre-heparin plasma activities of lipoprotein lipase and hepatic lipase together with correspondingly lower plasma free fatty acids. Mutants also exhibited elevated plasma IL-1β, TNF-α and CCL2 with a selective expansion of circulating monocytes, granulocytes and platelets, indicating a low-grade systemic inflammatory state already under chow conditions. After 8 weeks on a high-fat, cholesterol-enriched diet, mutants developed severe combined dyslipidemia, extensive aortic atherosclerosis with macrophage- and smooth-muscle-rich plaques, and marked hepatic steatosis. In conclusion, biallelic disruption of rabbit APOA5 produces a translationally relevant phenotype that recapitulates principal features of human APOA5 deficiency. The APOA5 mutant rabbit thus provides a tractable large-animal platform for studying residual cardiovascular risk and for evaluating emerging triglyceride-lowering therapeutics.
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Zha et al. (2026) studied Hypertriglyceridemia and atherosclerosis (n=10). Biallelic disruption of APOA5 via CRISPR/Cas9 was evaluated on Phenotypic development of dyslipidemia and atherosclerosis. Biallelic disruption of APOA5 in rabbits yielded 10 founders with an approximately 90% reduction in APOA5 protein, developing dyslipidemia on chow and severe atherosclerosis on a high-fat diet.
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