首页 | 本学科首页   官方微博 | 高级检索  
     

小鼠原代血管平滑肌细胞改良分离方法的建立
引用本文:张正杨,王含彦,易芳,田瑞敏,陈建业. 小鼠原代血管平滑肌细胞改良分离方法的建立[J]. 海南医学院学报, 2014, 0(3): 302-306,312
作者姓名:张正杨  王含彦  易芳  田瑞敏  陈建业
作者单位:[1]川北医学院生化教研室 [2]川北医学院药理教研室,四川南充637000
基金项目:四川省科技厅应用基础项目(2006J13-031).
摘    要:目的:建立方便、快速、高效的小鼠原代血管平滑肌细胞(vascular smooth muscle cell,VSMC)的分离培养方法,为相关研究提供快速获取原代VSMC的方法技术。方法:分离小鼠主动脉,用I型胶原酶消化血管组织去除内皮细胞等杂细胞;将血管切成1mm。大小组织块种植于六孔细胞培养板孔底,用分离培养液诱导原代VSMC细胞的繁殖生长。光学显微镜观察细胞形态特征;免疫组化方法鉴定VSMC特异性蛋白α-SMA的表达;RT—PCR方法检测VSMC特异性蛋白α-SMA和SM22α的mRNA表达水平。结果:本方法分离原代VSMC,3d后可见长梭状VSMC从组织块边缘长出,7d后可以进行传代。光学显微镜观察显示,分离细胞具有平滑肌细胞(smooth muscle cell,SMC)形态特征;免疫组化分析显示,分离细胞α—SMA蛋白表达阳性;RT—PCR分析显示,分离细胞中α-SMA和SM22α在mRNA水平高表达。结论:本实验成功建立了一种简便、快捷、高效从组织块分离培养VSMC的改良方法,为快速获得原代VSMC提供了一种适用的方法技术。

关 键 词:小鼠动脉血管  血管平滑肌细胞  组织块培养方法  原代细胞培养

Establishment of an improved method for the separation of original generation vascular smooth muscle cells from mice
ZHANG Zheng-yang,WANG Han-yan,YI Fang,TIAN Rui-min,CHEN Jian-ye. Establishment of an improved method for the separation of original generation vascular smooth muscle cells from mice[J]. Journal of Hainan Medical College, 2014, 0(3): 302-306,312
Authors:ZHANG Zheng-yang  WANG Han-yan  YI Fang  TIAN Rui-min  CHEN Jian-ye
Affiliation:1. Department of Biochemistry, North Sichuan Medical College ; 2. Department of Pharmacology , North Sichuan Medical College, Nanchong 637000, Sichuan, China)
Abstract:Objective=To establish a convenient, fast and efficient method for the separation of o- riginal generation vascular smooth muscle cells(VSMC) from mice, and also to provide a technical method to obtain the original generation VSMC quickly. Methods: Separated the mouse aorta, digest the vessel with collagenase Type I solution for the removal of endothelial cells and other miscellaneous cells which adhere to both inside and outside of the vessel. Cut the vessel into pieces, approximately (1 × 1) mm^2 in size and plant these pieces into the bottom of 6-well plate, induced the original generation VSMC to repro- duction and growth with separation medium. Observed the cell morphological characteristics with optical microscope, identified the expression of VSMC specific protein α-SMA by immunohistochemical method, and detected the VSMC specific gene expression of α-SMA and SM22α at mRNA level by RT-PCR. Re- suits. It can be observed that long fusiform VSMC was generated from tissue block edge after 3 days and could be passaged after 7 days using our method to separate the original generation VSMC. The separated cells have the typical morphological characteristics of smooth muscle cells (SMC) observed by optical mi- croscope. Immunohistochemical analysis showed that the expression of α-SMA protein in the separated cells is positive. It was proved by RT-PCR analysis that the expression of α-SMA and SM22α at mRNA level in the separated cells is higher. Conclusions. From what has been discussed above,this experiment successfully has established an improved method which can be used to separate the original generation VSMC from tissue pieces quickly and efficiently, and also provid an applicable technical method to quickly obtain original generation VSMC for scientific research.
Keywords:Mouse artery vascular  Vascular smooth muscle cell  Tissue pieces cultural method  Primary cell culture
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号