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用盐分离蝾螈肢体再生组织的上皮和间充质成分。

Separation of the epithelial and mesenchymal components of the newt limb regenerate with salt.

作者信息

Jasch L G

出版信息

J Exp Zool. 1979 Sep;209(3):443-54. doi: 10.1002/jez.1402090310.

Abstract

After incubation of isolated forelimb regenerates of Notophthalmus (Triturus) viridescens at all developmental stages for 60 minutes at 37 degrees C in a salt medium containing 111 mM sodium chloride, 5.6 mM potassium chloride and 100 mM sodium phosphate buffer at pH 7.5, the wound epithelium of each regenerate was removed intact from its underlying mesenchymal component. The suggestion is made that the salt medium is an effective epithelial-mesenchymal separating agent due to a combination of its hypertonicity, high ionic strength and the fact that the medium precipitates calcium as calcium phosphate. Attempts to dissect away the epithelium from the mesenchyme after incubation of isolated regenerates in sodium phosphate containing 1% or 3% Difco 1:250 trypsin, 10 mM EDTA or 150 units collagenase/ml medium were unsuccessful. Epidermis of adult newt forelimb skin was removed only after extended incubation of the forelimbs in the salt medium for three hours at 37 degrees C or after freezing isolated forelimbs in buffer and subsequent thawing.

摘要

将绿红东美螈(Notophthalmus (Triturus) viridescens)各发育阶段的离体前肢再生组织在含有111 mM氯化钠、5.6 mM氯化钾和100 mM磷酸钠缓冲液(pH 7.5)的盐培养基中于37℃孵育60分钟后,将每个再生组织的伤口上皮与其下方的间充质成分完整分离。有人认为,该盐培养基是一种有效的上皮 - 间充质分离剂,这是由于其高渗性、高离子强度以及该培养基会使钙沉淀为磷酸钙。将离体再生组织在含有1%或3% Difco 1:250胰蛋白酶、10 mM乙二胺四乙酸(EDTA)或150单位胶原酶/毫升培养基的磷酸钠中孵育后,试图从间充质中分离上皮,但未成功。成年蝾螈前肢皮肤的表皮只有在前肢于盐培养基中在37℃下延长孵育三小时后,或在缓冲液中冷冻离体前肢并随后解冻后才能去除。

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