SFRP4 Reduces Atherosclerosis Plaque Formation in ApoE Deficient Mice.

IF 1.8 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiology Research and Practice Pub Date : 2023-01-01 DOI:10.1155/2023/8302289
Hua Guan, Ting Liu, Miaomiao Liu, Xue Wang, Tao Shi, Fengwei Guo
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Abstract

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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SFRP4减少ApoE缺陷小鼠动脉粥样硬化斑块形成。
分泌卷曲相关蛋白4 (SFRP4)是SFRPs家族的一员,在代谢和心血管疾病中起重要作用。然而,没有足够的证据证明SFRP4在ApoE敲除(KO)小鼠中的抗动脉粥样硬化作用。给ApoE KO小鼠喂食西餐,并通过尾静脉注射腺病毒(Ad)-SFRP4,持续12周。与对照组相比,过表达SFRP4的ApoE KO小鼠的动脉粥样硬化斑块面积明显减少。Ad-SFRP4组血浆高密度脂蛋白胆固醇升高。RNA序列分析表明,在主动脉粥样硬化病变的mRNA谱中,存在96个富集于10条信号通路的差异表达基因。分析数据还揭示了与代谢、生物系统和人类疾病相关的一些基因的表达。总之,我们的数据表明,SFRP4可能在改善主动脉粥样硬化斑块形成中发挥重要作用。
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来源期刊
Cardiology Research and Practice
Cardiology Research and Practice Medicine-Cardiology and Cardiovascular Medicine
CiteScore
4.40
自引率
0.00%
发文量
64
审稿时长
13 weeks
期刊介绍: Cardiology Research and Practice is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies that focus on the diagnosis and treatment of cardiovascular disease. The journal welcomes submissions related to systemic hypertension, arrhythmia, congestive heart failure, valvular heart disease, vascular disease, congenital heart disease, and cardiomyopathy.
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