Department of Dental Implant Center, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing 100050, P.R. China.
Department of Integrated Emergency Dental Care, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing 100050, P.R. China.
Int J Mol Med. 2019 Feb;43(2):830-838. doi: 10.3892/ijmm.2018.4013. Epub 2018 Dec 3.
The present study aimed to investigate the effects of astragaloside IV on osteoblast‑like cell proliferation and migration, in addition to the underlying signaling pathway. In order to observe the effect on proliferation, a Cell Counting Kit‑8 assay and flow cytometry were used. To detect cell migration ability, cell scratch and Transwell cell migration assays were performed. The RNA and protein expression levels of hedgehog signaling molecules, including Sonic hedgehog (SHH) and GLI family zinc finger 1 (GLI1), were examined by reverse transcription‑quantitative polymerase chain reaction and western blot analyses. To inhibit the hedgehog signaling pathway, cyclopamine was used. Astragaloside IV, at a dosage of 1x10‑2 µg/ml in MG‑63 cells and 1x10‑3 µg/ml in U‑2OS cells, resulted in the enhanced proliferation and migration of cells, and the gene expression levels of the SHH and GLI1 were significantly increased. The combination of astragaloside IV and cyclopamine reduced MG‑63 and U‑2OS cell proliferation and migration, and inhibited the gene expression of SHH and GLI1. Astragaloside IV enhanced the proliferation and migration of human osteoblast‑like cells through activating the hedgehog signaling pathway. The results of the present study provide a rational for the mechanistic link in astragaloside IV promoting the proliferation and migration of osteoblasts via the hedgehog signaling pathway.
本研究旨在探讨黄芪甲苷对成骨样细胞增殖和迁移的影响及其潜在的信号通路。为了观察对增殖的影响,使用细胞计数试剂盒-8 检测和流式细胞术进行检测。为了检测细胞迁移能力,进行细胞划痕和 Transwell 细胞迁移实验。通过逆转录-定量聚合酶链反应和 Western blot 分析检测 hedgehog 信号分子的 RNA 和蛋白质表达水平,包括 Sonic hedgehog (SHH) 和 GLI 家族锌指蛋白 1 (GLI1)。为了抑制 hedgehog 信号通路,使用环巴胺。黄芪甲苷在 MG-63 细胞中的剂量为 1x10-2μg/ml 和 U-2OS 细胞中的剂量为 1x10-3μg/ml 时,可增强细胞的增殖和迁移,SHH 和 GLI1 的基因表达水平显著增加。黄芪甲苷和环巴胺的组合可降低 MG-63 和 U-2OS 细胞的增殖和迁移,并抑制 SHH 和 GLI1 的基因表达。黄芪甲苷通过激活 hedgehog 信号通路增强人成骨样细胞的增殖和迁移。本研究结果为黄芪甲苷通过 hedgehog 信号通路促进成骨细胞增殖和迁移的机制联系提供了依据。