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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.
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页码:321 / 329
页数:9
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