运行x2
Wnt信号通路
活力测定
细胞生长
转染
细胞周期
小RNA
成骨细胞
细胞生物学
化学
细胞分化
免疫印迹
细胞
分子生物学
生物
信号转导
生物化学
基因
体外
作者
Lin Chen,Xuefeng Huang,Xinchen Li,Tingxin Zhang,Chenguang Hao,Zhenyu Zhao
标识
DOI:10.1016/j.intimp.2019.106121
摘要
The research plans to make sure how Geniposide (GEN) functions in osteoblast proliferation and differentiation. The MC3T3-E1 and ATDC5 cells were treated with the GEN, XAV-939 and/or transfected with microRNA (miR)-214 mimic or corresponding control. Cell viability was detected with the CCK-8. The CyclinD1, Runx2, Osx, Ocn, Wnt3a and β-catenin were individually quantified via western blot. The cell cycle was tested by cell cycle analysis assay. The ALP activity was tested by ALP assay. qRT-PCR was used to examine the miR-214 expression level. The cell viability and the expressions of the CyclinD1, Runx2, Osx, Ocn Wnt3a and β-catenin, as well as the ALP activity were individually and significantly promoted by the GEN. Besides, miR-214 was down-regulated by the GEN. The XAV-939 or the miR-214 mimic destroyed the promotional effect of GEN on these elements above. In conclusion, GEN induced the proliferation and differentiation of the MC3T3-E1 and ATDC5 cells by targeting the miR-214 through Wnt/β-catenin activation.
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