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在原代皮肤培养中从成纤维细胞分离人表皮细胞。

Separation of human epidermal cells from fibroblasts in primary skin culture.

作者信息

Hentzer B, Kobayasi T

出版信息

Arch Dermatol Forsch. 1975;252(1):39-46. doi: 10.1007/BF00582429.

Abstract

To obtain pure culture of epidermal cells from small human biopsies, two different techniques were tested and compared, i.e. separation of epidermis from corium before cultivation by trypsin and suction, and after cultivation by trypsin and collagenase. The most active growth of epidermal cells was obtained by the third technique, since short-term trypsin treatment released only fibroblasts from the culture. Crude collagenase (type I) was less effective than trypsin. Collagenase type II, III and IV had no effect on fibroblast release. Neither trypsin nor collagenases dispersed epidermal cells.

摘要

为了从小的人体活检组织中获得表皮细胞的纯培养物,对两种不同的技术进行了测试和比较,即培养前通过胰蛋白酶和抽吸从真皮中分离表皮,以及培养后通过胰蛋白酶和胶原酶分离表皮。通过第三种技术获得了表皮细胞最活跃的生长,因为短期胰蛋白酶处理仅从培养物中释放出成纤维细胞。粗制I型胶原酶的效果不如胰蛋白酶。II型、III型和IV型胶原酶对成纤维细胞的释放没有作用。胰蛋白酶和胶原酶都不能分散表皮细胞。

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