Role of Transforming Growth Factor-β1 and Smads Signaling Pathway in Intrauterine Adhesion

被引:74
|
作者
Salma, Umme [1 ]
Xue, Min [1 ]
Sheikh, Md Sayed Ali [2 ]
Guan, Xiaoming [3 ]
Xu, Bin [1 ]
Zhang, Aiqian [1 ]
Huang, Lihua [4 ]
Xu, Dabao [1 ]
机构
[1] Cent S Univ, Xiangya Hosp 3, Dept Gynecol, 138 Tongzipo Rd, Changsha 410013, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Dept Cardiol, Changsha 410013, Hunan, Peoples R China
[3] Baylor Coll Med, Dept OB GYN, 6651 Main St,10th Floor, Houston, TX 77030 USA
[4] Cent S Univ, Xiangya Hosp 3, Ctr Med Expt, Changsha 410013, Hunan, Peoples R China
关键词
GROWTH-FACTOR-BETA; TGF-BETA; TRANSCRIPTIONAL ACTIVATION; CYSTIC-FIBROSIS; EXPRESSION; RECEPTOR; COLLAGEN; TRANSDUCTION; SCLERODERMA; DISEASE;
D O I
10.1155/2016/4158287
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of the study was to evaluate the role of Smad3, Smad7, and TGF-beta 1 in intrauterine adhesion (IUA) patients and experimental rabbit models. 60 IUA patients, 30 control participants, and 18 female rabbits were enrolled in this study. We found that the plasma concentrations and protein expressions of TGF-beta 1 were significantly increased in patients and experimental rabbits compared to those in controls (P < 0.05). Furthermore, the mRNA and protein expression levels of Smad3 were significantly elevated, while Smad7 level was markedly decreased in the patients and experimental rabbits compared with controls (P < 0.05). This altered ratio recommended that IUA was positively correlated to the mRNA and protein expression levels of Smad3, Smad7, and TGF-beta 1 in blood and uterine tissue. Moreover, we used the specific inhibitor of Smad3 (SIS3) in experimental rabbit. SIS3 obviously reduced the mRNA and protein expression of smad3 and TGF-beta 1, while it increased Smad7 expression in the treatment groups as compared with IUA rabbits (P < 0.05). Our study suggested that TGF-beta 1/Smad3/smad7 is a major pathway which plays an important role in the regulation of the IUA and specific inhibitor of Smad3 (SIS3) may provide a new therapeutic strategy for IUA.
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页数:13
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