Study on the Effects of Curculigoside on Proliferation, Differentiation, and Calcification of Mouse Osteoblastic MC3T3-E1 Cells

Wang Yin, Sun Qizhen, Ma Liyan
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引用次数: 5

Abstract

This study was aimed at evaluating the effects of Curculigoside (CCG) on the proliferation, differentiation, and calcification of mouse osteoblastic MC3T3-E1 cells. MTT assay was applied in the evaluation of MC3T3-E1 cell proliferation with CCG at different doses for different incubation periods. Alizarin red staining method was applied to observe the effect of CCG on the bone nodule formation of cells. The differentiating effects of CCG with different concentrations in cells were evaluated through the examination of alkaline phosphatase (ALP) activities by PNPP. The results showed that CCG is effective in promoting the proliferation of MC3T3-E1 cells cultured for 24 h, 48 h, and 72 h at doses ranging from 10−4 mol·L−1 to 10−8 mol·L−1. CCG at the concentration of 10−9 mol·L−1 remarkably increased the bone nodule formation of cells. The activity of ALP was stimulated by CCG at doses of 10−7 mol·L−1 and 10−9 mol·L−1 after 96 h of incubation. It was concluded that CCG has effects on stimulating the proliferation, differentiation, and calcification of MC3T3-E1 cells.

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莪术皂苷对小鼠成骨细胞MC3T3-E1增殖、分化及钙化影响的研究
本研究旨在探讨莪术皂苷(CCG)对小鼠成骨细胞MC3T3-E1增殖、分化和钙化的影响。采用MTT法评价不同剂量、不同潜伏期CCG对MC3T3-E1细胞增殖的影响。采用茜素红染色法观察CCG对骨结节细胞形成的影响。通过PNPP检测碱性磷酸酶(ALP)活性,评价不同浓度CCG对细胞的分化作用。结果表明,在10−4 mol·L−1 ~ 10−8 mol·L−1剂量范围内,CCG对培养24 h、48 h和72 h的MC3T3-E1细胞增殖均有促进作用。浓度为10−9 mol·L−1的CCG显著增加了骨细胞的结节形成。孵育96 h后,以10−7 mol·L−1和10−9 mol·L−1剂量的CCG刺激ALP活性。由此可见,CCG具有促进MC3T3-E1细胞增殖、分化和钙化的作用。
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