Article Summary
郝思雨 田江天 刘洋 张宇 党林 李吉.小鼠主动脉平滑肌细胞的分离培养及鉴定[J].现代生物医学进展英文版,2016,16(27):5237-5240.
小鼠主动脉平滑肌细胞的分离培养及鉴定
Isolated Culture and Identification of Mouse Aortic Vascular Smooth Muscle Cell
  
DOI:
中文关键词: 小鼠  血管平滑肌细胞  原代培养  鉴定
英文关键词: Mouse  Vascular smooth muscle cell  Primary culture  Identification
基金项目:国家自然科学基金面上项目(81573042)
Author NameAffiliation
郝思雨 田江天 刘洋 张宇 党林 李吉 哈尔滨医科大学附属第二医院皮肤科哈尔滨医科大学附属第二医院心内科心肌缺血省部共建教育部重点实验室哈尔滨医科大学附属第二医院静脉用药调配中心 
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中文摘要:
      目的:建立分离培养小鼠原代主动脉血管平滑肌细胞(VSMC)的方法并检测其生长特性。方法:剥离小鼠主动脉中膜层,分 别采用组织块培养法及胶原酶消化法分离培养小鼠主动脉来源的原代VSMC,免疫荧光法检测细胞的纯度和分化状态;3-(4,5- 二甲基-2-噻唑)-2,5-二苯基溴化四氮唑蓝(MTT)法测定小鼠主动脉VSMC 传代细胞的生长、增殖特性。结果:组织块培养法培 养组织块8d 后,细胞从组织块边缘爬出,18 d后细胞汇合度达到80 %以上后传代;胶原酶消化法分离培养的细胞生长7 d后,汇 合度可达80 %,此时进行传代;2 种方法获得的细胞进行免疫荧光染色,结果显示细胞传至第3 代时纯度在95 %以上,传至第8 代时分化状态并没有改变;MTT 法显示细胞生长3~5 d时处于指数生长期。结论:本研究建立了2 种可靠稳定的分离和培养小鼠 主动脉VSMC 的方法,VSMC 纯度高,多次传代后细胞特征稳定。
英文摘要:
      Objective:To establish the technical method of isolated culture mouse aorta vascular smooth muscle cell (VSMC) in vitro and observe their growth characteristics.Methods:The mouse aorta middle layer was isolated, VSMC of original generation separation from aorta in mice by tissue piece inoculation and collagenase digestion method were compared and characterized by immunofluorescence; The growth and proliferation characteristics of passage VSMC were measured by growth curve method, 3-(4,5-dimethyl-2-thiahiazo)- 2,5-diphenyltetrazolium bromide (MTT).Results:After cells were cultured for 8 days with tissue piece inoculation method, VSMC were slowly grown from the tissue edge and confluence reached to 80 %at 18 days and could be passaged. After cells were cultured for 7 days with collagenase digestion method, the cells confluence reached to more than 80 % and were passaged. Immunofluorescence staining showed the purity was more than 95 % after 3 passages, keeping their differentiation state until 8 passages; MTT assay showed that optical density change of cell growth was obvious at 3~5 days.Conclusion:Two kinds of efficient isolation methods were established to culture pure and stable mouse aortic VSMC.
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