Osthole decreases collagen I/III contents and their ratio in TGF-β1-overexpressed mouse cardiac fibroblasts through regulating the TGF-β/Smad signaling pathway

被引:26
|
作者
Liu Jin-Cheng [1 ,2 ]
Zhou Lei [3 ]
Wang Feng [2 ]
Cheng Zong-Qi [1 ]
Rong Chen [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Dept Pharm, Clin Pharmacol Lab, Suzhou 215006, Peoples R China
[2] Soochow Univ, Coll Pharmaceut Sci, Dept Pharmacol, Jiangsu Key Lab Prevent & Translat Med Geriatr Di, Suzhou 215123, Peoples R China
[3] Wuxi Ctr Dis Control & Prevent, Lab Dept, Wuxi 214023, Peoples R China
关键词
Osthole; TGF-beta; 1; Collagen; Mouse cardiac fibroblasts; HYPERTENSIVE HEART-DISEASE; INDUCED FATTY LIVER; GROWTH-FACTOR-BETA; MESENCHYMAL TRANSITION; RENAL FIBROSIS; MICE; TRANSFECTION; EXPRESSION; TGF-BETA-1; CELLS;
D O I
10.1016/S1875-5364(18)30063-3
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The present study was designed to elucidate whether the mechanism by which osthole decreases collagen I/III contents and their ratio is regulating the TGF-beta/Smad signaling pathway in TGF-beta 1-overexpressed mouse cardiac fibroblasts (CFs). These CFs were cultured and treated with different concentrations of osthole. Our results showed that the TGF-beta 1 expression in the CFs transfected with that the recombinant expression plasmids pcDNA3.1(+)-TGF-beta 1 was significantly enhanced. After the CFs were treated with 1.25-5 mu g.mL(-1) of osthole for 24 h, the mRNA and protein expression levels of collagens I and III were reduced. The collagen I/III ratio was also reduced. The mRNA and protein expression levels of TGF-beta 1, T beta R I, Smad2/3, P-Smad2/3, Smad4, and alpha-SMA were decreased, whereas the expression level of Smad7 was increased. These effects suggested that osthole could inhibit collagen I and III expression and reduce their ratio via the TGF-beta/Smad signaling pathway in TGF-beta 1 overexpressed CFs. These effects of osthole may play beneficial roles in the prevention and treatment of myocardial fibrosis.
引用
收藏
页码:321 / 329
页数:9
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