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作 者:孙剑瑞[1] 王琳[2] 王树凯[1] 殷德涛[3] 宋来君[1] 杨波[1]
机构地区:[1]郑州大学第一附属医院神经外科,450052 [2]郑州大学第一附属医院信息科,450052 [3]郑州大学第一附属医院甲状腺外科,450052
出 处:《中华实验外科杂志》2012年第5期946-948,共3页Chinese Journal of Experimental Surgery
基 金:河南省卫生科技创新型人才工程专项经费资助项目(201052);河南省高校青年骨干教师资助项目(2011GGJS-014)
摘 要:目的优化脐血单核细胞(UCB-MNCs)的培养方法。方法采用正交实验方法筛选影响UCB.MNCs培养的各因素,优化培养条件。设立优化组、对照组(UCB-MNCs以1.0×10^6/L接种于含20μg/L碱性成纤维细胞生长因子(bFGF)、体积分数为0.10胎牛血清、低糖DMEM培养基)培养。其后检测各组培养细胞增殖及形态学变化;流式细胞仪对各组行免疫表型分析。结果筛选后优化培养条件为:低糖DMEM培养基中含20mg/LbFGF、50μg/L干细胞因子(SCF)、10峙/L重组人粒细胞生长因子(G—CSF)、培养瓶用层粘连蛋白(LN)包被。原代培养的细胞密度优化组细胞(108.15±6.90)增殖优于对照组(51.48±12.27),差异有统计学意义(P〈0.01)。P3代UCB—MNCs中MSCs含量优化组(94.87%)优于对照组(75.35%),差异有统计学意义(P〈0.05)。结论采用正交实验的方法可以筛选出脐血单核细胞的优化培养条件。Objective To optimize the culture method of umbilical cord blood-mononuclear cells (UCB-MNCs). Methods First, crosscut empirical method was employed to sieve culture factors of UCB-MNCs, optimize the culture condition. Set up optimize group and control group [ UCB-MNCs was plated in 1.0 ×10^6/L Lo CHO DMEM supplemented with 20 I.Lg/L basic fibroblast growth factor (bFGF), 10% FBS)]. Then generation and morphology was detected. Immunophenotype was analysesed by FCM. Results The sieved optimized cultivate condition: culture flask was coating by laminin (LN), UCB-MNCs was plated in it ( 1.0 ×10^6/L) containing Lo CHO DMEM supplemented with 10 μg/L granulocyte colony stimulating factor (G-CSF), 50 p.g/L stem cell factor (SCF), 20 μg/L bFGF, 20 ml/L B27. Optimize group ( 108. 15 ±6. 90) Compared to the control group (51.48 ± 12. 27) , cell proliferation was more significant (P 〈0. 01 ), P3 UCB-MNCs content more MSCs in optimized group. Conclusion Optimized cultivate condition of UCB-MNCs could be sieved by orthogonal experiment.
分 类 号:R329[医药卫生—人体解剖和组织胚胎学]
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