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补肾活血方通过miR-483对Wnt通路的调控来调节椎间盘退变中髓核细胞增殖和细胞外基质重塑。

Bu-Shen-Huo-Xue-Fang modulates nucleus pulposus cell proliferation and extracellular matrix remodeling in intervertebral disk degeneration through miR-483 regulation of Wnt pathway.

作者信息

Yang Shaofeng, Li Linghui, Zhu Liguo, Zhang Chao, Li Zhaoyong, Guo Yantao, Nie Ying, Luo Zhenhua

机构信息

Department of Spine, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.

Department of General Orthopedics, Wangjing Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

J Cell Biochem. 2019 Dec;120(12):19318-19329. doi: 10.1002/jcb.26760. Epub 2019 Aug 25.

DOI:10.1002/jcb.26760
PMID:29393545
Abstract

Intervertebral disk degeneration (IDD) has been widely considered as one of the main causes for low back pain, which can cause a severe impact to human health and huge economic burden to worldwide society. IDD pathogenesis can be affected by extensive degradation of extracellular matrix (ECM) and the hyperproliferation of nucleus pulposus (NP) cells. During the IDD process, expression of the ECM degradation enzymes matrix metalloproteinase and ADAMTS increases, whereas expression of ECM synthesis-related aggrecan and COL2A1 decreases. In addition, the Wnt signaling pathway is reportedly involved in the process of IDD. Bu-Shen-Huo-Xue-Fang (BSHXF), a Chinese traditional medicine formula that contains six Chinese traditional medicinal herbs, is widely used in the treatment of IDD. Herein, we obtained the serum containing BSHXF from BSHXF-fed rat and demonstrated that the BSHXF promoted NP cell proliferation and ECM synthesis through the Wnt signaling pathway. By using DIANA online tools and luciferase reporter gene assays, we confirmed that miR-483-3p and miR-23c regulated CTNNB1 and GSK3B, respectively, through direct targeting, thereby affecting the effect of BSHXF on NP cell proliferation and ECM synthesis through the Wnt signaling pathway. Taken together, we demonstrated the function and mechanism of BSHXF in regulating NP cell proliferation and ECM remodeling through the Wnt signaling pathway during IDD.

摘要

椎间盘退变(IDD)已被广泛认为是腰痛的主要原因之一,它会对人类健康造成严重影响,并给全球社会带来巨大的经济负担。IDD的发病机制可能受细胞外基质(ECM)广泛降解和髓核(NP)细胞过度增殖的影响。在IDD过程中,ECM降解酶基质金属蛋白酶和含血小板反应蛋白基序的解聚素样金属蛋白酶的表达增加,而与ECM合成相关的聚集蛋白聚糖和COL2A1的表达减少。此外,据报道Wnt信号通路参与了IDD的过程。补肾活血方(BSHXF)是一种由六种中药组成的中药方剂,广泛用于IDD的治疗。在此,我们从喂食BSHXF的大鼠中获得了含BSHXF的血清,并证明BSHXF通过Wnt信号通路促进NP细胞增殖和ECM合成。通过使用DIANA在线工具和荧光素酶报告基因测定,我们证实miR-483-3p和miR-23c分别通过直接靶向调控CTNNB1和GSK3B,从而影响BSHXF通过Wnt信号通路对NP细胞增殖和ECM合成的作用。综上所述,我们证明了BSHXF在IDD过程中通过Wnt信号通路调节NP细胞增殖和ECM重塑的功能及机制。

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