Chen Wei, Li Cihui, Wu Shu, Xie Huiqi, Luo Jingcong
Division of Stem Cell and Tissue Engineering, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, PR China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2010 Jan;24(1):94-9.
To investigate the effect of machine-enzyme digestion method on the residual quantity of small intestinal submucosa (SIS) cell and the content of growth factors.
Fresh jejunum of pig within 4 hours after harvesting was prepared into SIS after machine digestion (removing placenta percreta, mucosa, and muscular layer), decrease, trypsinization, abstergent processing, and freeze drying. Samples were kept after every preparation step serving as groups A, B, C, D, and E, respectively (n=4 per group). And the fresh jejunum served as control group (group F, n=4). The histological alteration in each preparation process was reviewed with HE staining and scanning electron microscope (SEM). Nest-polymerase chain reaction (PCR) was used to determine the content of death associated protein 12 (DAP12), and enzyme-linked immunosorbent assay (ELISA) was applied to detect the content of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), transforming growth factor beta (TGF-beta), tumor necrosis factor alpha (TNF-alpha).
HE staining and SEM observation showed that there were residual cells in groups A and B, and there were no residual cells in groups C, D, and E. Nest-PCR test revealed the occurrence of DAP12 in each group. The contents of DAP12 in groups A, B, C, D, E, and F were (18.01 +/- 9.53), (11.87 +/- 2.35), (0.59 +/- 0.27), (0.29 +/- 0.05), (0.19 +/- 0.04), and (183.50 +/- 120.13) copy x 10(6)/cm2. The content of DAP12 in group F was significant higher than that of other groups (P < 0.05), groups A and B was higher than groups C, D, and E (P < 0.05), there were significant differences among groups C, D, and E (P < 0.05), and there was no significant difference between groups A and B (P > 0.05). The ELISA test showed the content of VEGF, bFGF, TGF-beta, and TNF-alpha in group A was significantly higher than that of groups B, C, D, and E (P < 0.05), and there was no significant difference among groups B, C, D, and E (P > 0.05).
SIS prepared by simple mechanical method has more residual cells, while the machine-enzyme digestion method can effectively remove the cells and significantly reduce the DAP12 content. This approach can not obviously reduce the growth factor content in SIS.
探讨机械 - 酶消化法对小肠黏膜下层(SIS)细胞残留量及生长因子含量的影响。
将猪收获后4小时内的新鲜空肠经机械消化(去除胎盘、黏膜和肌层)、减量、胰蛋白酶处理、清洗处理及冻干后制成SIS。在每个制备步骤后留取样本,分别作为A、B、C、D和E组(每组n = 4)。新鲜空肠作为对照组(F组,n = 4)。用苏木精 - 伊红(HE)染色和扫描电子显微镜(SEM)观察各制备过程中的组织学改变。采用巢式聚合酶链反应(PCR)测定死亡相关蛋白12(DAP12)的含量,并用酶联免疫吸附测定(ELISA)检测血管内皮生长因子(VEGF)、碱性成纤维细胞生长因子(bFGF)、转化生长因子β(TGF - β)、肿瘤坏死因子α(TNF - α)的含量。
HE染色和SEM观察显示,A组和B组有残留细胞,C组、D组和E组无残留细胞。巢式PCR检测显示各组均有DAP12表达。A、B、C、D、E和F组DAP12的含量分别为(18.01±9.53)、(11.87±2.35)、(0.59±0.27)、(0.29±0.05)、(0.19±0.04)和(183.50±120.13)拷贝×10(6)/cm2。F组DAP12含量显著高于其他组(P < 0.05),A组和B组高于C组、D组和E组(P < 0.05),C组、D组和E组之间差异有统计学意义(P < 0.05),A组和B组之间无显著差异(P > 0.05)。ELISA检测显示,A组VEGF、bFGF、TGF - β和TNF - α的含量显著高于B、C、D和E组(P < 0.05),B、C、D和E组之间无显著差异(P > 0.05)。
单纯机械方法制备的SIS残留细胞较多,而机械 - 酶消化法能有效去除细胞并显著降低DAP12含量。该方法不会明显降低SIS中生长因子的含量。