Abstract
AbstractObjectiveAtherosclerosis, the main pathology underlying cardiovascular diseases is accelerated in diabetic patients. Genetic mouse models require breeding efforts which are time-consuming and costly. To establish a new non-genetic model of inducible metabolic risk factors mimicking hyperlipidemia, hyperglycemia, or both and allowing to detect phenotypic differences dependent on the metabolic stressor(s).Methods and ResultsWild type mice were injected with gain-of-function PCSK9D377Y (proprotein convertase subtilisin/kexin type 9) mutant adeno-associated viral particles (AAV) and streptozotocin and fed either a high-fat diet (HFD) or high-cholesterol/high fat-diet (Paigen diet, PD). Combined hyperlipidemic and hyperglycemic (HGHCi) mice, but not hyperlipidemia (HCi) alone, display characteristic features of accelerated atherosclerosis. Atherosclerotic plaques of HGHCi animals were larger, showed a less stable phenotype, contained more macrophages and less smooth muscle cells. These findings were observed both at early (12 weeks) and late (20 weeks) time points on both HFD or PD diet. Differences between the HGHCi and HCi model were confirmed using RNAseq analysis revealing that significantly more genes are dysregulated in mice with combined hyperlipidemia and hyperglycemia as compared to the hyperlipidemia only group. The HGHCi-associated genes were related to pathways regulating inflammation, cellular metabolism and collagen degradation. PD accelerates atherosclerosis in mice and shows plaque formation already after 8 weeks, therefore, representing a fast direct inducible hyperglycemic atherosclerosis model.ConclusionWe established a non-genetic inducible mouse model allowing comparative analyses of atherosclerosis in HCi and HGHCi conditions and its modification by diet, allowing analyses of multiple metabolic hits in mice.
Publisher
Cold Spring Harbor Laboratory
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