SFRP4 Reduces Atherosclerosis Plaque Formation in ApoE Deficient Mice

被引:2
|
作者
Guan, Hua [1 ,2 ,3 ]
Liu, Ting [4 ]
Liu, Miaomiao [5 ]
Wang, Xue [5 ]
Shi, Tao [5 ]
Guo, Fengwei [5 ]
机构
[1] Xi An Jiao Tong Univ, Lab Anim Ctr, Hlth Sci Ctr, Xian 710061, Shaanxi, Peoples R China
[2] Xian Med Univ, Shaanxi Key Lab Ischem Cardiovasc Dis, Xian 710021, Shaanxi, Peoples R China
[3] Xian Med Univ, Inst Basic & Translat Med, Xian 710021, Shaanxi, Peoples R China
[4] Xian Fourth Hosp, Xian Peoples Hosp, Dept Nephrol, Xian 710004, Shaanxi, Peoples R China
[5] Xi An Jiao Tong Univ, Dept Cardiovasc Surg, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
OXIDATIVE STRESS; PROTEIN; 4; INFLAMMATION; METABOLISM; THROMBOSIS; EXPRESSION; FAMILY; GENE;
D O I
10.1155/2023/8302289
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Secreted frizzled related protein 4 (SFRP4), a member of the SFRPs family, contributes to a significant function in metabolic and cardiovascular diseases. However, there is not enough evidence to prove the antiatherosclerosis effect of SFRP4 in ApoE knock-out (KO) mice. ApoE KO mice were fed a western diet and injected adenovirus (Ad)-SFRP4 through the tail vein for 12 weeks. Contrasted with the control cohort, the area of atherosclerotic plaque in ApoE KO mice overexpressing SFRP4 was reduced significantly. Plasma high-density lipoprotein cholesterol was elevated in the Ad-SFRP4 group. RNA sequence analysis indicated that there were 96 differentially expressed genes enriched in 10 signaling pathways in the mRNA profile of aortic atherosclerosis lesions. The analysis data also revealed the expression of a number of genes linked to metabolism, organism system, and human disease. In summary, our data demonstrates that SFRP4 could play an important role in improving atherosclerotic plaque formation in the aorta.
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页数:10
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