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兔子宫内膜分离细胞类型的放射性碘化表面蛋白与着床时间的关系。

Radioiodinated surface proteins of separated cell types from rabbit endometrium in relation to the time of implantation.

作者信息

Ricketts A P, Scott D W, Bullock D W

出版信息

Cell Tissue Res. 1984;236(2):421-9. doi: 10.1007/BF00214246.

Abstract

To investigate changes in surface proteins of uterine cells in relation to the time of implantation, epithelial and stromal cells were isolated from rabbit endometrium and maintained in primary culture for 3 days. Surface-iodination of intact cells was carried out before and after culture, using immobilized Iodogen catalyst. The labeled proteins were analyzed by polyacrylamide gel electrophoresis, followed by autoradiography; peak areas were quantitated by scanning densitometry. Different gestational ages showed no marked qualitative differences in the surface-iodination patterns either of epithelial or stromal cells before or after culture. Quantitative differences between the surface-iodination pattern of epithelial cells from days 4 to 6.5 of pregnancy were revealed by canonical variate analysis of labeled peak areas. Values for individual rabbits clustered according to gestational age, with significant (p less than 0.05) separation of the clusters, although the discrimination was less pronounced for cultured than for freshly isolated cells. Changes involving increases in labeling of a protein of 38000 Mr in fresh cells, and decreases in a protein of 42000 Mr in cultured cells, were evident between day 4 and day 6.5. Thus changes in the surface-labeling pattern of uterine epithelial cells in relation to the time of receptivity for ovoimplantation can be distinguished. The functional significance of these changes remains to be elucidated.

摘要

为了研究子宫细胞表面蛋白与着床时间的关系,从兔子宫内膜分离出上皮细胞和基质细胞,并进行原代培养3天。在培养前后,使用固定化碘代甘氨酸催化剂对完整细胞进行表面碘化。标记的蛋白质通过聚丙烯酰胺凝胶电泳进行分析,随后进行放射自显影;峰面积通过扫描密度计进行定量。不同妊娠年龄在培养前后上皮细胞或基质细胞的表面碘化模式上均未显示出明显的定性差异。通过对标记峰面积的典型变量分析揭示了妊娠第4天至6.5天上皮细胞表面碘化模式的定量差异。尽管培养细胞的区分不如新鲜分离细胞明显,但各个兔子的值根据妊娠年龄聚类,聚类之间有显著(p小于0.05)的分离。在第4天和第6.5天之间,新鲜细胞中38000 Mr蛋白质标记增加而培养细胞中42000 Mr蛋白质标记减少的变化很明显。因此,可以区分子宫上皮细胞表面标记模式与卵着床接受时间相关的变化。这些变化的功能意义仍有待阐明。

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