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胶原酶灌注法制备小鼠肝细胞
引用本文:赵粤萍,周云,张军,刘广超,马远方.胶原酶灌注法制备小鼠肝细胞[J].河南大学学报(医学版),2008,27(3).
作者姓名:赵粤萍  周云  张军  刘广超  马远方
作者单位:1. 河南大学,天然药物与免疫工程省级重点实验室,河南,开封,475003
2. 河南大学,免疫学研究所,河南,开封,475003
基金项目:河南省高校杰出科研创新人才工程项目,河南省医学重大科技攻关计划项目
摘    要:目的:建立体外培养小鼠肝细胞的实验体系。方法:采用两步原位胶原酶灌注法分离小鼠肝细胞,在RPM I1640培养液中培养。结果:用胶原酶灌注法分离的小鼠肝细胞活率可达90%以上,产量平均为2.8×107,完全满足实验要求。肝细胞在RPM I1640培养液中2 h即可贴壁,48 h内细胞贴壁充分,伸展良好,1周后死细胞增多。结论:胶原酶灌注法成功制备出小鼠肝细胞。

关 键 词:胶原酶  肝细胞  分离

On the production of mouse hepatocytes by perfusion with collagenase
ZHAO Yue-ping,ZHOU Yun,ZHANG Jun,LIU Guang-chao,MA Yuan-fang.On the production of mouse hepatocytes by perfusion with collagenase[J].Journal of Henan University,2008,27(3).
Authors:ZHAO Yue-ping  ZHOU Yun  ZHANG Jun  LIU Guang-chao  MA Yuan-fang
Institution:ZHAO Yue-ping,ZHOU Yun,ZHANG Jun,LIU Guang-chao,MA Yuan-fang*(1.Naturally Occurring Drugs , Immuno-engineering Key Laboratory of Henan University,Kaifeng 475003,China,2.Institute of Immunology,Henan University,China)
Abstract:Objective: To establish experimental system of mouse hepatocytes culture in vitro.Methods: Mouse hepatocytes were isolated by a two-step perfusion with collagenase in situ,and cultured in RPMI1640.Results: The cells viability(90%) and yield(×107) could meet the requirement of experiment.The cells attachment was noted after 2 h incubation in RPMI1640.During the following 48h,the cells attached completely,and extended well,but the death cells increased one week later.Conclusion: Mouse hepatocytes can be prepared by perfusion with collagenase successfully.
Keywords:Collagenase  Hepatocyte  Isolation  
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