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兔角膜内皮细胞的新法培养
作者:杨鹏1 刘瑶2 曾水林1 张会保1 
单位:1.东南大学医学院人体解剖学教研室; 2.东南大学医学院眼科学教研室
关键词:角膜 内皮细胞 细胞培养  
分类号:Q813.1
出版年·卷·期(页码):2001·20·第三期(170-172)
摘要:

目的:介绍一种全新的角膜内皮细胞培养方法.方法:在体视显微镜下撕下角膜后弹力层及内皮细胞层并剪切成小块,分置于培养皿中,将盖玻片叠加在组织块上进行培养.结果:角膜内皮细胞很快自组织块迁移生长.结论:本法培养内皮细胞不需用酶,具有简便、可靠、不易污染、细胞量大的优势,值得推广.

Objective  To introduce a new method to culture corneal endothelial cells.Methods  Through stero  microscope,Descemet’s membrane and endothelial cell layer were torn apart and cut out into small pieces,then the pieces were put into culture containers and coverglasses were piled up on tissue pieces for culture.Results  The corneal endothelial cells were transformed quickly from tissue pieces.Conclusion  Enzyme is not required in this method,moreover,the method has many advantages,such as simple,reliable,pollution  proof and high  yield.In a word,it is a good method worth recommending.

参考文献:

[1] STOCKER F W, EIRING A, GEORGING R. A tissue culture technique for growing corneal epithelial stromal,and endothelial tissues separately, 1958(5)
[2] SLICK W C, MANNAGH J, YUHASZ Z. Enzymatic removal and pure culture of rabbit corneal endothelial cells, 1965(2)
[3] 谢立信, 董晓光, 张德茹. 兔角膜组织细胞培养的技术改进, 1990(4)
[4] Baum J L, NIEDRA R, DAVIS C. Mass culture of human corneal endothelial cells, 1979(6)
[5] Perlman M, BAUM J, KAYE G I. Fine structure and collagen synthesis activity of monolayer culture of rabbit corneal endothelium. 1974(2). doi:10.1083/jcb.63.1.306  

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