SFRP4 Reduces Atherosclerosis Plaque Formation in ApoE Deficient Mice

Author:

Guan Hua12ORCID,Liu Ting3ORCID,Liu Miaomiao4ORCID,Wang Xue4ORCID,Shi Tao4ORCID,Guo Fengwei4ORCID

Affiliation:

1. Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, Shaanxi 710061, China

2. Shaanxi Key Laboratory of Ischemic Cardiovascular Diseases & Institute of Basic and Translational Medicine, Xi’an Medical University, Xi’an 710021, Shaanxi, China

3. Department of Nephrology, Xi’an People’s Hospital (Xi’an Fourth Hospital), Xi’an 710004, Shaanxi, China

4. Department of Cardiovascular Surgery, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an 710061, Shaanxi, China

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.

Funder

Natural Science Foundation of Shaanxi Province

Publisher

Hindawi Limited

Subject

Cardiology and Cardiovascular Medicine

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