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SD大鼠肾小管上皮细胞两种原代培养及传代方法的比较
引用本文:杜胜华,唐德燊,刘华锋.SD大鼠肾小管上皮细胞两种原代培养及传代方法的比较[J].湛江医学院学报,2005,23(1):10-13.
作者姓名:杜胜华  唐德燊  刘华锋
作者单位:广东医学院肾病研究所,广东湛江,524023;广东医学院肾病研究所,广东湛江,524023;广东医学院肾病研究所,广东湛江,524023
基金项目:广东医学院博士启动基金 (2 0 0 2年 )
摘    要:目的:建立较理想的大鼠肾小管上皮细胞原代培养、传代及鉴定方法。方法:采用肾小管节段贴块法及0.2%胰蛋白酶消化20min两种方法进行原代培养,以0.25%胰蛋白酶(A组)、0.125%胰蛋白酶-0.02%EDTA(B组)消化传代,利用免疫细胞化学方法鉴定细胞种类。结果:两种方法均能成功培养肾小管上皮细胞,但前者较好,小管节段贴壁早。B组成功传代(4代)并鉴定为肾小管上皮细胞,A组传代失败。结论:肾小管节段贴块、0.125%胰蛋白酶-0.02%EDTA消化是大鼠肾小管上皮细胞原代培养及传代的有效方法。

关 键 词:肾小管上皮细胞  细胞培养  免疫细胞化学
文章编号:1005-4057(2005)01-0010-04
修稿时间:2004年3月15日

Comparison of primary and passage cultures for renal tubular epithelial cells in SD rat
DU Sheng-hua,TANG De-shen,LIU Hua-feng.Comparison of primary and passage cultures for renal tubular epithelial cells in SD rat[J].Journal of Guangdong Medical College,2005,23(1):10-13.
Authors:DU Sheng-hua  TANG De-shen  LIU Hua-feng
Abstract:Objective:To establish a practical method for primary and passage cultures in rat renal cells. Methods: Both segmental sticking of renal tubule from SD rats and digestion with 0.2% trypsin for 20 minutes were used in primary culture. Digestion with 0.25% trypsin (Group A) or with 0.125% trypsin plus 0.02% EDTA (Group B) was applied in passage culture. Cell types were identified by immunocytochemistry. Results: Two methods for primary culture were successful, but the segmental sticking was better. The passage culture was only seen in Group A, and 4 generations were achieved. Conclusion: The segmental sticking of renal tubule and digestion with 0.125% trypsin plus 0.02% EDTA are eligible methods for primary and passage cultures in rat renal cells, respectively.
Keywords:renal tubular epithelial cell  cell culture  immunocytochemistry
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