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器官培养中重组小鼠磨牙牙胚合成的釉质蛋白的测定

Determination of enamel protein synthesized by recombined mouse molar tooth germs in organ culture.

作者信息

Baba T, Terashima T, Oida S, Sasaki S

机构信息

Department of Oral Biochemistry, School of Dentistry, Nagasaki University, Japan.

出版信息

Arch Oral Biol. 1996 Feb;41(2):215-9. doi: 10.1016/0003-9969(95)00120-4.

Abstract

Epithelial-mesenchymal interaction is a prerequisite for tooth morphogenesis. To study this interaction, inner enamel epithelium and dental papilla mesenchyme of molar tooth germs from a 16.5-day mouse embryo were dissociated enzymatically and cultured alone or after recombination. Characteristic matrix protein synthesized and secreted by recombined tooth germ was determined quantitatively by enzyme-linked immunosorbent assay. The protein was detected in the culture of recombined tooth germ but not of dissociated enamel epithelium alone. The amount of enamel protein increased until 8 days in culture. Morphological differentiation of the recombined epithelial rudiment into ameloblasts and enamel protein production were confirmed.

摘要

上皮-间充质相互作用是牙齿形态发生的前提条件。为研究这种相互作用,将16.5天龄小鼠胚胎磨牙牙胚的内釉上皮和牙乳头间充质进行酶解分离,单独培养或重组后培养。通过酶联免疫吸附测定法定量测定重组牙胚合成和分泌的特征性基质蛋白。该蛋白在重组牙胚培养物中可检测到,而在单独解离的釉上皮培养物中未检测到。釉蛋白量在培养8天前增加。证实了重组上皮原基向成釉细胞的形态分化及釉蛋白的产生。

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