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[胰蛋白酶对大鼠角质形成细胞分离及传代培养的影响]

[Effect of trypsin on the rat keratinocyte separation and subculture].

作者信息

Ouyang An-Li, Zhou Yan, Hua Ping, Tan Wen-Song

机构信息

State Key Laboratory of Bioreactor Engineering, ECUST, Shanghai 200237, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2002 Jan;18(1):59-62.

Abstract

The effect of trypsin on the separation an subculture of the keratinocytes was investigated in this work. It was found that when 0.25% trypsin was employed for 5 minutes to separate keratinocytes, the number of active keratinocytes and the cells capable of forming colony were higher than those of other experimental conditions. The maximum attached ratio of primary keratinocytes was obtained when skin tissues were treated at 0.05% concentration of trypsin. With the increase of the trypsin concentrations, the attached ratio, attachment rate constant, and colony forming efficiency were all increased. Thus, 0.25% concentration of trypsin was recommended for separating and subculturing the keratinocytes.

摘要

本研究探讨了胰蛋白酶对角质形成细胞分离和传代培养的影响。结果发现,当使用0.25%胰蛋白酶处理5分钟来分离角质形成细胞时,活性角质形成细胞数量和能够形成集落的细胞数量均高于其他实验条件下的数量。当以0.05%浓度的胰蛋白酶处理皮肤组织时,原代角质形成细胞的最大贴壁率得以实现。随着胰蛋白酶浓度的增加,贴壁率、贴壁速率常数和集落形成效率均升高。因此,推荐使用浓度为0.25%的胰蛋白酶来分离和传代培养角质形成细胞。

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