Liu Xinyu, Song Xiaobin, Zhang Peng, Zhu Zhenkun, Xu Xin
Stomatological College of Shandong University, Jinan, Shandong 250012, P.R. China; Shandong Province Key Laboratory of Oral Biology Medicine, Jinan, Shandong 250012, P.R. China; Department of Stomatology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, P.R. China.
Department of Stomatology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, P.R. China.
Exp Ther Med. 2016 Dec;12(6):3541-3544. doi: 10.3892/etm.2016.3801. Epub 2016 Oct 12.
In the present study, we examined the effects of nano tantalum (Ta) dental implants on inducing osteoblast proliferation and differentiation. The MG-63 osteoblasts were divided into 3 groups after recovery, passage and storage: i) Osteoblast culturing group (control group); ii) osteoblast and titanium (Ti) implant co-culturing group (Ti group); and iii) osteoblast and Ta implant co-culturing group (Ta group). After 7 days, a scanning electron microscope was used to observe the growth status, number and morphological changes of the cells on the surfaces of the materials. An MTT assay was used to detect cell proliferation after culturing for 1, 3 and 7 days. ELISA assay was used to detect the levels of alkaline phosphatase (ALP) after 1, 3 and 7 days. Western blot analysis was used to detect the expression levels of collagen type I (Col-1) and osteocalcin after 1, 3 and 7 days. There was significant cell spreading on the surfaces of Ti and of Ta after 7 days, flat and with many pseudopodia. Additionally, there were more cell components in the Ta group. Concurrently, cell proliferation in the Ti and Ta groups increased. There was also an increase in the level of ALP and the expression level of Col-1 over time. The indexes of the Ta group were more apparent than those of the Ti group at each time-point, and the differences were statistically significant (p<0.05). In conclusion, compared with Ti implants, Ta implants induced more osteoblast proliferation and differentiation.
在本研究中,我们检测了纳米钽(Ta)牙科植入物对诱导成骨细胞增殖和分化的影响。MG-63成骨细胞复苏、传代和保存后分为3组:i)成骨细胞培养组(对照组);ii)成骨细胞与钛(Ti)植入物共培养组(Ti组);iii)成骨细胞与Ta植入物共培养组(Ta组)。7天后,用扫描电子显微镜观察材料表面细胞的生长状态、数量及形态变化。采用MTT法检测培养1、3和7天后的细胞增殖情况。采用ELISA法检测1、3和7天后碱性磷酸酶(ALP)水平。采用蛋白质免疫印迹分析检测1、3和7天后I型胶原(Col-1)和骨钙素的表达水平。7天后,Ti和Ta表面均有明显的细胞铺展,细胞扁平且有许多伪足。此外,Ta组的细胞成分更多。同时,Ti组和Ta组的细胞增殖均增加。随着时间的推移,ALP水平和Col-1表达水平也有所增加。各时间点Ta组的指标均比Ti组更明显,差异具有统计学意义(p<0.05)。综上所述,与Ti植入物相比,Ta植入物诱导更多的成骨细胞增殖和分化。