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// Xian-Yi Zeng 1, 2, 4, * , Yan-Qiong Zhang 2, 5, * , Xiao-Min He 2, 4, * , Lin-Yan Wan 1, 2, 3, 4, 5, * , Hu Wang 1, 2, 3, 4 , Yi-Ran Ni 2 , Jie Wang 2 , Jiang-Feng Wu 1, 2, 3, 4, 5 , Chang-Bai Liu 1, 2, 3, 4, 5 1 The Institute of Cell Therapy, China Three Gorges University, Yichang, 443000, China 2 Medical College, China Three Gorges University, Yichang, 443002, China 3 The First People’s Hospital of Yichang, Hubei Yichang, 443000, China 4 Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, Yichang, 443002, China 5 Institute of Liver Diseases, China Three Gorges University, Yichang, 443002, China * These authors contributed equally to this work Correspondence to: Jiang-Feng Wu, email: wujiangfeng@ctgu.edu.cn Chang-Bai Liu, email: cbliu@ctgu.edu.cn Keywords: hepatic fibrosis, TGF-β, BMP-7, miR-23b/27b cluster, siRNA Received: September 24, 2016 Accepted: November 08, 2016 Published: November 15, 2016 ABSTRACT The imbalance between transforming growth factor β and bone morphogenetic protein 7 signaling pathways is a critical step in promoting hepatic stellate cell activation during hepatic fibrogenesis. Gremlin1 may impair the balance. Something remains unclear about the regulatory mechanisms of gremlin1 action on hepatic stellate cell activation and hepatic fibrosis. In the current study, gremlin1 overexpression promotes activation of hepatic stellate cells. Knockdown of gremlin1 with siRNAs suppresses hepatic stellate cell activation and attenuates hepatic fibrosis in rat model. Our results also show that miR-23b/27b cluster members bind to 3′-untranslated region of gremlin1 resulting in reduction of transforming growth factor β, α-smooth muscle actin and collagenI α1/2 gene expression. Our findings suggest that gremlin1 promotes hepatic stellate cell activation and hepatic fibrogenesis through impairment of the balance between transforming growth factor β and bone morphogenetic protein 7 signaling pathways. The miR-23b/27b cluster suppresses activation of hepatic stellate cells through binding gremlin1 to rectify the imbalance.
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Zeng et al. (2016) studied this question.
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