Increased Legumain/Smad3 expression in atherosclerotic plaque of rat thoracic aorta

Biomedicine & Pharmacotherapy

Chengcheng Duan¹  Shaoyuan Chen²  Wen Ai³  Hongcheng Fang³  Lei Wang³  Yeqing Fang³  Rongzhi Liu³  Peiyi Xie³ 

[1] Shenzhen Nanshan Medical Group Headquarters, Shenzhen, 518052, China;Department of Cardiology, Shajing Hospital, Guangzhou Medical University, Shenzhen, 518104, China;Department of Cardiology, Shenzhen Nanshan People’s Hospital, Guangdong Medical University, Shenzhen, 518052, China;

关键词: Legumain;    Smad3;    Atherosclerosis;    Inflammatory response;    Macrophages;   

DOI  :  

来源: DOAJ

【 摘 要 】

Objectives: The purpose of this study was to investigate the role of legumain in the formation and stability of atherosclerotic plaque, as well as to explore the association between legumain with Smad3 pathway in a rat atherosclerosis model. Methods: Rat with thoracic aorta atherosclerosis was established and received treatment with statin (n = 15 each) or controls (n = 10). Serum level of legumain was determined by enzyme-linked immunosorbent assay. Legumain and Smad3 aortic expression levels were assessed by immunohistochemistry and fluorescence microscopy. Protein and mRNA levels were analyzed using Western blot analysis and reverse transcriptase coupled polymerase chain reaction, respectively. Results: The atherosclerotic group showed higher serum legumain level than control and statin group. Expression of legumain and Smad3 in macrophages and foam cells was increased in atherosclerotic group compared to control and statin group. The protein and mRNA levels of legumain and Smad3 were significantly attenuated by statin treatment (p < 0.05). For all groups, legumain expression was correlated linearly with Smad3 at mRNA (coefficient: 0.94) and protein (coefficient: 097) level. Conclusions: Legumain and Smad3 expression is highly expressed in mainly atherosclerotic plaque macrophages and linearly related, which is attenuated by statin therapy, suggesting legumain a potential Smad3 pathway-related marker of atherosclerosis.

【 授权许可】

Unknown