Chinese Journal of Tissue Engineering Research ›› 2014, Vol. 18 ›› Issue (30): 4797-4803.doi: 10.3969/j.issn.2095-4344.2014.30.007
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Xu Fan, Yang De-sheng
Revised:
2014-05-28
Online:
2014-07-16
Published:
2014-08-08
Contact:
Yang De-sheng, Master’s supervisor, Chief physician, Department of Stomatology, General Hospital of the Chinese People’s Armed Police Force, Beijing 100039, China
About author:
Xu Fan, Studying for master’s degree, Department of Stomatology, General Hospital of the Chinese People’s Armed Police Force, Beijing 100039, China
Supported by:
a grant from General Hospital of the Chinese People’s Armed Police Force, No. WZ2012008
CLC Number:
Xu Fan, Yang De-sheng. Effect of Bio-Gide collagen membranes on the proliferation and osteogenetic differentiation of rabbit bone marrow mesenchymal stem cells[J]. Chinese Journal of Tissue Engineering Research, 2014, 18(30): 4797-4803.
2.2 细胞增殖情况 CCK-8检测细胞吸光度值数据见表1,数据经两独立样本t 检验行统计学分析;以时间、A值为坐标,绘制细胞增殖曲线,见图3。图中可以看出,随着培养时间的增加,两组细胞数量均不断增加,第1-4天细胞处于生长适应期,第1,4天两组细胞数量比较无明显差异(P > 0.05);第4-7天细胞处于对数生长期,细胞大量增殖,在第7天两组细胞数量比较差异有显著性意义(P < 0.05),实验组细胞少于对照组;随着培养时间的增加,第7-14天细胞逐渐进入生长平台期,在第14天两组细胞数量比较差异无显著性意义(P > 0.05),说明Bio-Gide胶原膜适宜骨髓间充质干细胞的生长,可以作为骨髓间充质干细胞增殖的载体。"
2.3 细胞碱性磷酸酶活性 碱性磷酸酶检测数据见表2,数据采用两独立样本t 检验行统计学分析;以时间、A值为坐标,绘制细胞碱性磷酸酶活性图,见图4。如图所示,两组细胞在成骨分化诱导液的诱导下,细胞向成骨方向分化,两组细胞碱性磷酸酶活性随着培养时间的增加不断升高,在成骨分化诱导的第1,4,7天,两组细胞碱性磷酸酶活性比差异无显著性意义(P > 0.05),但在第14天,实验组细胞碱性磷酸酶活性高于对照组(P < 0.05),说明在成骨分化诱导条件下,两组细胞均逐渐具有成骨分化能力,但实验组细胞成骨分化能力更强,说明与Bio-Gide胶原膜复合培养更有利于干细胞的成骨分化,随着培养时间的增加,Bio-Gide胶原膜对经成骨分化诱导干细胞的细胞碱性磷酸酶活性有促进作用。"
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