Department of Stomatology, General Hospital of the Yangtze River Shipping, and Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430010, PR China.
Mol Med Rep. 2012 Sep;6(3):547-52. doi: 10.3892/mmr.2012.974. Epub 2012 Jun 29.
Dental pulp stem cells (DPSCs) have the potential to form bone, nerve and fat, and are a candidate for use in regenerative medicine. Previous studies indicated that total flavonoids from Drynaria fortunei show a stimulative effect on the proliferation and osteogenic differentiation of osteoblastic MC3T3-E1 cells in vitro. This study aimed to investigate the effect of total flavonoids from Drynaria fortunei on the proliferation and osteogenic differentiation of rat DPSCs, and to further clarify the mechanisms involved. DPSCs were isolated by enzymatic digestion and identified using the CD44, CD29 and CD34 markers by immunohistochemistry, and exposed to 0.01, 0.05 and 0.1 g/l total flavonoids from Drynaria fortunei media. Total flavonoids from Drynaria fortunei promoted the proliferation of DPSCs in a dose-dependent manner and this effect may depend on the shortening of the G0/G1 phase and promotion of the S phase. Compared with the control group, the levels of alkaline phosphatase (ALP) and the expression of osteogenic genes increased with the concentrations of total flavonoids from Drynaria fortunei, and the volume and number of calcified nodules in the Drynaria groups was bigger compared to the control group. These results suggest that total flavonoid from Drynaria fortunei directly stimulates DPSC proliferation and osteogenic differentiation, and may serve as a new promising candidate drug for dental tissue engineering and bone regeneration.
密鳞凤仙花总黄酮促进大鼠牙髓干细胞增殖及成骨分化的作用及机制研究
密鳞凤仙花总黄酮具有促进成骨细胞 MC3T3-E1 增殖及成骨分化的作用,本研究旨在观察密鳞凤仙花总黄酮对大鼠牙髓干细胞(DPSCs)增殖及成骨分化的影响,并探讨其作用机制。
采用酶消化法分离培养大鼠 DPSCs,免疫细胞化学鉴定 CD44、CD29、CD34 表达。分别给予 0.01、0.05、0.1 g/L 密鳞凤仙花总黄酮干预,CCK-8 法检测 DPSCs 增殖情况,流式细胞术检测细胞周期,比色法检测碱性磷酸酶(ALP)活性,茜素红染色检测矿化结节形成,实时荧光定量 PCR 检测成骨相关基因表达。
结果显示,密鳞凤仙花总黄酮呈浓度依赖性促进 DPSCs 增殖,且能促进 DPSCs 由 G0/G1 期进入 S 期。与对照组相比,密鳞凤仙花总黄酮能增加 DPSCs 碱性磷酸酶活性及成骨相关基因的表达,茜素红染色结果显示密鳞凤仙花总黄酮能促进矿化结节形成。
综上,密鳞凤仙花总黄酮能直接促进 DPSCs 增殖及成骨分化,有望成为组织工程中促进牙组织及骨再生的新型候选药物。