机构:[1]Department of Orthopaedics, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Baiyun District, Guangzhou, Guangdong 510405, China深圳市中医院深圳医学信息中心[2]Key Laboratory of Orthopaedics & Traumatology, Guangzhou University of Chinese Medicine, Guangzhou 510405, China深圳市中医院深圳医学信息中心[3]Guangdong Provincial Academy of Chinese Medical Sciences, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510120, China广东省中医院[4]Department of Anatomy, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China深圳市中医院深圳医学信息中心
Icariin, the major ingredient of Herba Epimedii, promotes the osteogenic differentiation of rat bone marrow stromal cells (rBMSCs) and exerts protective effects against bone loss and increases bone regeneration, but the underlying signaling pathway by which icariin affects osteogenic differentiation remain unclear. Transcriptional coactivator with PDZ-binding motif (TAZ) is a transcriptional modulator of the Hippo signaling pathway, which plays an important role in the osteogenic differentiation of BMSCs by activating Runx2 gene during the terminal osteogenic differentiation. In this study, we found that 0.1 mu M icariin markedly promoted the proliferation, calcium depositions, and osteogenic genes expression of rBMSCs. Icariin (0.1 mu M) upregulated TAZ, Runx2, beta-catenin, Osteopotin, and Dlx5 expression mainly at the early stage of osteogenic differentiation, and increased osteocalcin expression at the late stage. Our result further demonstrated that knockdown TAZ expression by lentivirus-mtdediated TAZ shRNA inhibited the icariin-induced osteogenic differentiation. Moreover, ICI 182780 (the estrogen receptor alpha inhibitor) or DKK1 (the Wnt/beta-catenin pathway inhibitor), inhibited the icariin-induced increase in TAZ expression. Furthermore, icariin stimulated the activation of TAZ as evidenced by increased total TAZ protein and nuclear translocation, but these effects of icariin were blocked by ICI 182780 or DKK1. Taken together, our results demonstrate that icariin promotes the osteogenic differentiation of rBMSCs by increasing TAZ expression, and that the increased TAZ expression induced by icariin is mostly mediated by the ERa and Wnt/beta-catenin pathway. (C) 2017 Published by Elsevier Masson SAS.
基金:
project of the National Natural Science Foundation of ChinaNational Natural Science Foundation of China [81302994, 81473697, 81574002, 81273778]; GZUCM Science Fund for Creative Research Groups [2016KYTD10]; GZUCM Torch Program [A1-AFD015142Z08]
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外文
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中科院(CAS)分区:
出版当年[2016]版:
大类|3 区医学
小类|4 区医学:研究与实验4 区药学
最新[2025]版:
大类|2 区医学
小类|2 区医学:研究与实验2 区药学
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出版当年[2015]版:
Q3MEDICINE, RESEARCH & EXPERIMENTALQ3PHARMACOLOGY & PHARMACY
最新[2023]版:
Q1MEDICINE, RESEARCH & EXPERIMENTALQ1PHARMACOLOGY & PHARMACY
第一作者机构:[1]Department of Orthopaedics, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Baiyun District, Guangzhou, Guangdong 510405, China[2]Key Laboratory of Orthopaedics & Traumatology, Guangzhou University of Chinese Medicine, Guangzhou 510405, China
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通讯作者:
通讯机构:[1]Department of Orthopaedics, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Baiyun District, Guangzhou, Guangdong 510405, China[2]Key Laboratory of Orthopaedics & Traumatology, Guangzhou University of Chinese Medicine, Guangzhou 510405, China[4]Department of Anatomy, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China
推荐引用方式(GB/T 7714):
Wei QiuShi,He MinCong,Chen MeiHui,et al.Icariin stimulates osteogenic differentiation of rat bone marrow stromal stem cells by increasing TAZ expression[J].BIOMEDICINE & PHARMACOTHERAPY.2017,91:581-589.doi:10.1016/j.biopha.2017.04.019.
APA:
Wei, QiuShi,He, MinCong,Chen, MeiHui,Chen, ZhenQiu,Yang, Fan...&He, Wei.(2017).Icariin stimulates osteogenic differentiation of rat bone marrow stromal stem cells by increasing TAZ expression.BIOMEDICINE & PHARMACOTHERAPY,91,
MLA:
Wei, QiuShi,et al."Icariin stimulates osteogenic differentiation of rat bone marrow stromal stem cells by increasing TAZ expression".BIOMEDICINE & PHARMACOTHERAPY 91.(2017):581-589