SFRP4 Reduces Atherosclerosis Plaque Formation in ApoE Deficient Mice.
Hua GuanTing LiuMiaomiao LiuXue WangTao ShiFengwei GuoPublished in: Cardiology research and practice (2023)
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.
Keyphrases
- cardiovascular disease
- cognitive decline
- high fat diet
- high fat diet induced
- coronary artery disease
- aortic valve
- electronic health record
- endothelial cells
- signaling pathway
- poor prognosis
- pulmonary artery
- oxidative stress
- insulin resistance
- south africa
- machine learning
- type diabetes
- gene expression
- adipose tissue
- coronary artery
- big data
- metabolic syndrome
- data analysis
- single cell
- dna methylation
- epithelial mesenchymal transition
- genome wide identification
- heart failure
- bioinformatics analysis
- induced apoptosis
- endoplasmic reticulum stress
- binding protein
- amino acid
- atrial fibrillation
- preterm birth
- pulmonary hypertension