Zhu Huiyong, Sun Lei, Chen Jianfen, Wang Huiming
Department of Oral and Maxillofacial Surgery, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou Zhejiang, 310003, P.R. China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2009 Jul;23(7):845-50.
To compare the effect of two different methods of cell seeding on spatial distribution and gene expression of hBMSCs in biocoral scaffold in vitro cultures.
The composite of hBMSCs and biocoral scaffold was prepared by traditional seeding (group A) and fibrin glue seeding (group B). The seeding efficiency was measured after 30 minutes of incubation in group B and after 3 hours in group A. At 2, 7, 14 and 21 days after culture, the samples were harvested and the serial longitudinal sections were cut for each embedded composite. The sections were stained with DAPI and were measured using fluorescence microscope with apostome under serial optical sections. The cell number in every 10 x objective field was automatically measured by AxioVision image analysis software and levels (from seeding surface to bottom L1-L5) or columns (from centre to margin) for comparing cell distribution were set up. The specific osteogenic genes [osteonectin (ON), core binding factor alpha1 (Cbfalpha1), osteocalcin (OC)] expression was measured by RT-PCR.
The seeding efficiency was significantly higher in group B (88.32% +/- 4.2%) than in group A (66.51% +/- 12.33%, P < 0.01). At 2 days after culture, the cell number from L1 to L4 decreased gradully in two groups (P < 0.05); in the cell number of different columns, there was no significant difference in group A (P > 0.05) whereas significant difference in group B (P < 0.05); there was no significant difference in gene expression between two groups (P > 0.05). At 7 days after culture, the cell number was less than that at 2 days in group A and there was significant difference among levels (P < 0.05). The cell number and osteogenic gene expression increased sharply and there appeared uniform cell distribution in group B (P > 0.05). The gene expression of ON and Cbfalpha1 in group B was higher than that in group A (P < 0.05). At 14 days after culture, the cell number in levels or columns in group A decreased sharply and was less than that at 7 days (P < 0.05); whereas the cell number was similar to that at 7 days in group B (P > 0.05). The OC gene expression reached the highest level in group B at 14 days. The gene expression was higher in group B than in group A (P < 0.05). At 21 days after culture, there was significant difference in the cell number among levels and in the gene expression between group A and group B (P < 0.05); there was no significant difference in the cell number among columns in two groups (P > 0.05). In addition, the cell number of most levels and columns in group B was more than that in group A at 7, 14 and 21 days after culture (P < 0.05).
More uniform cell distribution with rapid proliferation and osteogenic differentiation is available in different levels or columns of scaffold by fibrin glue seeding than by traditional seeding.
比较两种不同细胞接种方法对体外培养的生物珊瑚支架中hBMSCs空间分布和基因表达的影响。
采用传统接种法(A组)和纤维蛋白胶接种法(B组)制备hBMSCs与生物珊瑚支架复合物。B组孵育30分钟后、A组孵育3小时后测定接种效率。培养2、7、14和21天后,收获样本,对每个包埋复合物进行连续纵向切片。切片用DAPI染色,在连续光学切片下用带孔阑的荧光显微镜进行测量。通过AxioVision图像分析软件自动测量每10倍物镜视野下的细胞数,并设置用于比较细胞分布的水平(从接种表面到底部L1-L5)或柱(从中心到边缘)。通过RT-PCR检测特异性成骨基因[骨连接蛋白(ON)、核心结合因子α1(Cbfalpha1)、骨钙素(OC)]的表达。
B组接种效率(88.32%±4.2%)显著高于A组(66.51%±12.33%,P<0.01)。培养2天时,两组从L1到L4的细胞数均逐渐减少(P<0.05);在不同柱的细胞数方面,A组无显著差异(P>0.05),而B组有显著差异(P<0.05);两组基因表达无显著差异(P>0.05)。培养7天时,A组细胞数少于2天时,各水平间有显著差异(P<0.05)。B组细胞数和成骨基因表达急剧增加,细胞分布均匀(P>0.05)。B组ON和Cbfalpha1基因表达高于A组(P<0.05)。培养14天时,A组水平或柱中的细胞数急剧减少,且少于7天时(P<0.05);而B组细胞数与7天时相似(P>0.05)。B组OC基因表达在14天时达到最高水平。B组基因表达高于A组(P<0.05)。培养21天时,A、B组水平间细胞数和基因表达有显著差异(P<0.05);两组柱间细胞数无显著差异(P>0
.05)。此外,培养7、14和21天时,B组大多数
水平和柱的细胞数多于A组(P<0
.05)。
与
传统接种
法
相比,纤维
蛋白胶接种
法可使支架
不同水平
或柱
中细胞分布更均匀,并具有快速增殖和成骨分化能力。