期刊
JOURNAL OF THE AMERICAN HEART ASSOCIATION
卷 9, 期 1, 页码 -出版社
WILEY
DOI: 10.1161/JAHA.119.014358
关键词
fatty acid beta-oxidation; hyperlipidemia; proprotein convertase subtilisin; kexin type 9; renal fibrosis; vaccine
资金
- Major Research Plan of the National Natural Science Foundation of China [91439207]
- National Natural Science Foundation of China [81900459, 81770366, 81670461, 81500388]
Background Defects in the renal fatty acid beta-oxidation pathway have been implicated in the development of renal fibrosis. Our group has developed a therapeutic vaccine targeting PCSK9 (proprotein convertase subtilisin/kexin type 9), named PCSK9Q beta-003. In this study, we investigated the potential effectiveness of the PCSK9Q beta-003 vaccine on hypercholesterolemia with renal fibrosis. Methods and Results The low-density lipoprotein receptor(+/-) male mice fed with a high-cholesterol (1%) Western diet were randomly assigned into 4 groups: the sham group (or the control group), the phosphate-buffered saline group, the Q beta virus-like particles group and the PCSK9Q beta-003 vaccine group. Mice of the PCSK9Q beta-003 group were injected with the PCSK9Q beta-003 vaccine (100 mu g/time) every 2 or 4 weeks. The mice were administered with either unilateral ureteral obstruction for 2 weeks or N-nitro-l-arginine methyl ester (50 mg/kg per day) for 6 weeks to establish a renal fibrosis model. Compared with the other 3 groups, the PCSK9Q beta-003 vaccine obviously decreased total cholesterol and low-density lipoprotein cholesterol in low-density lipoprotein receptor(+/-) mice with hypercholesterolemia. Compared with the phosphate-buffered saline and Q beta virus-like particles groups, the PCSK9Q beta-003 vaccine improved hepatic steatosis and renal function. Histology analysis showed that the PCSK9Q beta-003 vaccine significantly ameliorated renal lipid accumulation and renal fibrosis. Moreover, the PCSK9Q beta-003 vaccine obviously upregulated the expression of low-density lipoprotein receptor, very-low-density lipoprotein receptor, sterol-regulatory element binding protein 2, and fatty acid beta-oxidation-related factors, and ameliorated renal fibrosis-related molecules both in the unilateral ureteral obstruction and N-nitro-l-arginine methyl ester models. Conclusions This study suggested that the PCSK9Q beta-003 vaccine improved renal lipid accumulation and renal fibrosis by regulating fatty acid beta-oxidation, which may provide a promising method for treating hypercholesterolemia with renal fibrosis.
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