Yang Jing, Xiang Zhou, Wei Daiqing, Huang Xiao, Gao Yu, Gao Bo, Shu Tao, Duan Xin, Zhang Xingdong
Department of Orthopaedics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P R China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013 Aug;27(8):916-22.
To investigate the protocols of combined culture of human placenta-derived mesenchymal stem cells (HPMSCs) and human umbilical vein endothelial cells (HUVECs) from the same and different individuals on collagen material,to provide the.
Under voluntary contributions, HPMSCs were isolated and purified from human full-term placenta using collagenase IV digestion and lymphocyte separation medium, and confirmed by morphology methods and flow cytometry, and then passage 2 cells were cultured under condition of osteogenic induction. HUVECs were isolated from fresh human umbilical vein by collagenase I digestion and subcultured to purification, and cells were confirmed by immunocytochemical staining of von Willebrand factor (vWF). There were 2 groups for experiment. Passage 3 osteoblastic induced HPMSCs were co-cultured with HUVECs (1:1) from different individuals in group A and with HUVECs from the same individual in group B on collagen hydrogel. Confocal laser scanning microscope was used to observe the cellular behavior of the cell-collagen composites at 1, 3, 5, and 7 days after culturing.
Flow cytometry showed that HPMSCs were strongly positive for CD90 and CD29, but negative for CD31, CD45, and CD34. After induction, alizarin red, alkaline phosphatase, and collagenase I staining were positive. HUVECs displayed cobble-stone morphology and stained positively for endothelial cell marker vWF. The immunofluorescent staining of CD31 showed that HUVECs in the cell-collagen composite of group B had richer layers, adhered and extended faster and better in three-dimension space than that of group A. At 7 days, the class-like microvessel lengths and the network point numbers were (6.68 +/- 0.35) mm/mm2 and (17.10 +/- 1.10)/mm2 in group A, and were (8.11 +/- 0.62) mm/mm2 and (21.30 +/- 1.41)/mm2 in group B, showing significant differences between the 2 groups (t = 0.894, P = 0.000; t = 0.732, P = 0.000).
Composite implant HPMSCs and HUVECs from the same individual on collagen hydrogel is better than HPMSCs and HUVECs from different individuals in integrity and continuity of the network and angiogenesis.
研究人胎盘来源间充质干细胞(HPMSCs)与来自同一及不同个体的人脐静脉内皮细胞(HUVECs)在胶原材料上的联合培养方案,以提供……
在自愿捐献情况下,采用IV型胶原酶消化及淋巴细胞分离培养基从人足月胎盘中分离并纯化HPMSCs,通过形态学方法和流式细胞术进行鉴定,然后将第2代细胞在成骨诱导条件下培养。采用I型胶原酶消化从新鲜人脐静脉中分离HUVECs并传代培养至纯化,通过血管性血友病因子(vWF)免疫细胞化学染色对细胞进行鉴定。实验分为2组。将第3代成骨诱导的HPMSCs与来自不同个体的HUVECs(1:1)在A组胶原水凝胶上共同培养,与来自同一个体的HUVECs在B组胶原水凝胶上共同培养。采用共聚焦激光扫描显微镜观察培养1、3、5和7天后细胞 - 胶原复合物的细胞行为。
流式细胞术显示HPMSCs对CD90和CD29呈强阳性,而对CD31、CD45和CD34呈阴性。诱导后,茜素红、碱性磷酸酶和I型胶原酶染色呈阳性。HUVECs呈鹅卵石样形态,内皮细胞标志物vWF染色呈阳性。CD31免疫荧光染色显示,B组细胞 - 胶原复合物中的HUVECs层数更丰富,在三维空间中黏附及伸展更快且更好,优于A组。7天时,A组类微血管长度和网络点数分别为(6.68±0.35)mm/mm²和(17.10±1.10)/mm²,B组分别为(8.11±0.62)mm/mm²和(21.30±1.41)/mm²,两组间差异有统计学意义(t = 0.894,P = 0.000;t = 0.732,P = 0.000)。
在胶原水凝胶上复合植入来自同一个体的HPMSCs和HUVECs,在网络完整性和连续性以及血管生成方面优于来自不同个体的HPMSCs和HUVECs。