miRNA-338-3p/CDK4 signaling pathway suppressed hepatic stellate cell activation and proliferation

BMC Gastroenterology - Tập 17 - Trang 1-9 - 2017
Bensong Duan1, Jiangfeng Hu1, Tongyangzi Zhang2, Xu Luo3, Yi Zhou3, Shun Liu4, Liang Zhu3, Cheng Wu5, Wenxiang Liu6, Chao Chen6, Hengjun Gao7,8
1Department of Gastroenterology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China
2Department of Respiration, Tongji Hospital, Tongji University School of Medicine, Shanghai, China
3Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai, China
4Department of Epidemiology, School of Public Health, Guangxi Medical University, Nanning, China
5Digestive Endoscopic Center, Department of Gastroenterology, South Building General Hospital of PLA, Beijing, China
6Department of Gastroenterology, First Affiliated Hospital of Chinese PLA General Hospital, Beijing, China
7National Engineering Center for Biochip at Shanghai, Shanghai, China
8Department of Gastroenterology, Institute of Digestive Diseases, Tongji University School of Medicine, Shanghai, China

Tóm tắt

Activated hepatic stellate cell (HSC) is the main fibrogenic cell type in the injured liver. miRNA plays an important role in activation and proliferation of HSC. Our previous study examined the expression profiles of microRNAs in quiescent and activated HSC. Real-time PCR and western blot were used to detect the expression of Collagen type I (Col 1) and Alpha-Smooth Muscle Actin (α-SMA). CCK-8 and Edu assay was used to measure the proliferation rate of HSC. Luciferase reporter gene assay was used to tested the binding between miR-338-3p and Cyclin-dependent kinase 4 (CDK4). We found overexpression of miR-338-3p could inhibit Col 1 and α-SMA, two major HSC activation markers, whereas miR-338-3p inhibitor could promote them. Besides, miR-338-3p overexpression could suppress the growth rate of HSC. Further, we found that CDK4, a pleiotropic signaling protein, was a direct target gene of miR-338-3p. Moreover, we found that overexpression of CDK4 could block the effects of miR-338-3p. We found miR-338-3p is an anti-fibrotic miRNA which inhibits cell activation and proliferation. Our findings suggest that miR-338-3p/CDK4 signaling pathway participates in the regulation of HSC activation and growth and may act as a novel target for further anti-fibrotic therapy.

Tài liệu tham khảo

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