Xie L X
Department of Ophthalmology, Weifang Medical College, Shandong Province.
Zhonghua Yan Ke Za Zhi. 1990 Jul;26(4):237-9.
A simplified technique for short-term culture of pure populations of rabbit corneal epithelial or endothelial cells has been developed. Rabbit corneas were placed on the concave agarose surfaces of a 24 well culture plate, treated briefly with a solution of trypsin and ethylenediamine tetracetic acid, and transferred, epithelial surface or endothelial surface down as needed, to another 24 well culture plate. Within 24 hours, the epithelial cells or endothelial cells grew over the surfaces of the wells. This technique is simple and economical for the initiation of primary culture of rabbit corneal epithelial or endothelial cells for use in various experiments.
已开发出一种用于兔角膜上皮细胞或内皮细胞纯群体短期培养的简化技术。将兔角膜置于24孔培养板的凹形琼脂糖表面,用胰蛋白酶和乙二胺四乙酸溶液短暂处理,然后根据需要将上皮表面或内皮表面朝下转移至另一个24孔培养板。在24小时内,上皮细胞或内皮细胞在孔表面生长。该技术对于启动用于各种实验的兔角膜上皮或内皮细胞原代培养而言简单且经济。