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提高新生大鼠原代心肌细胞纯度方法的探讨
引用本文:王新陆,崔琳,王幼平,李彬,谢世阳,朱明军. 提高新生大鼠原代心肌细胞纯度方法的探讨[J]. 世界科学技术-中医药现代化, 2015, 17(2): 333-337
作者姓名:王新陆  崔琳  王幼平  李彬  谢世阳  朱明军
作者单位:河南中医学院 郑州 450000,河南中医学院第一附属医院 郑州 450000,河南中医学院第一附属医院 郑州 450001,河南中医学院第一附属医院 郑州 450002,河南中医学院第一附属医院 郑州 450003,河南中医学院第一附属医院 郑州 450004
基金项目:国家自然科学基金委面上项目(81173410):参加优化方通过TGF-β/smads通路改善心梗后心室重构作用机制的研究,负责人:朱明军;国家自然科学基金委面上项目(81373853):参附益心颗粒通过抑制Ang Ⅱ改善心梗后心衰大鼠心肌代谢重构的机制研究,负责人:朱明军;河南省高校科技创新团队支持计划(13IRTSTHN012),负责人:朱明军。
摘    要:目的:探讨提高新生大鼠原代心肌细胞纯度的方法。方法:应用0.08%心肌细胞消化液重复消化出生第1-3天乳鼠的心肌组织多次;收集的细胞用含10%胎牛血清的DMEM培养基中和。用差速贴壁分离法分离后,加入红细胞裂解液,以除去红细胞,加入溴脱氧尿嘧啶(Brdu)纯化心肌细胞后置CO2培养箱孵育2天,无血清同步化1天。结果:分离1只乳鼠获得的心肌细胞产量约为1.2×106个,有活力心肌细胞占90%以上,心肌细胞纯度>90%,3-4天后心肌细胞融合成片,并出现自发性节律性搏动。结论:该方法在保证心肌细胞产量和心肌细胞活性的同时,能大幅度提高心肌细胞纯度。

关 键 词:新生大鼠  心肌细胞  原代培养  鉴定
收稿时间:2014-03-03
修稿时间:2015-01-19

Discussion on Improving Purity of Primary Myocardial Cells from Neonatal Rats
Wang Xinlu,Cui Lin,Wang Youping,Li Bin,Xie Shiyang and Zhu Mingjun. Discussion on Improving Purity of Primary Myocardial Cells from Neonatal Rats[J]. World Science and Technology—Modernization of Traditional Chinese Medicine and Materia Medica, 2015, 17(2): 333-337
Authors:Wang Xinlu  Cui Lin  Wang Youping  Li Bin  Xie Shiyang  Zhu Mingjun
Affiliation:Henan University of Traditional Chinese Medicine, Zhengzhou 450000, China,The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450000, China,The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450001, China,The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450002, China,The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450003, China and The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450004, China
Abstract:This study was aimed to explore the method to improve the purity of primary myocardial cells from neonatal rats. The myocardial tissues of rats which were born 1-3 days were repeated digested by 0.08% myocardial cells digestive juices. And then, cells were neutralized with DMEM medium which containing 10% fetal bovine serum. The cells were separated with differential sidewall ion. The red blood cell cracking liquid was added to remove the red blood cells. Bromine deoxidization uracil (Brdu) was added to purify the myocardial cells. Then, cells were incubated in the CO2 incubator for two days. The serum-free synchronization was performed for one day. The results showed that the output of myocardial cells from one rat was about 1.2 × 106. The dynamic myocardial cells occupied more than 90%. The purity of myocardial cells was more than 90%. After 3 to 4 days, the cell fusion of myocardial cells was formed with spontaneous rhythm beats. It was concluded that the method can ensure the yield and the activity of the myocardial cells. At the same time, the purity of myocardial cells can also be improved greatly.
Keywords:Neonatal rat   myocardial cell   primary culture   identification
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