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在含有或不含有山羊抗大鼠胎盘IgG的培养基中培养的大鼠卵黄囊脏层上皮的精细结构和胞饮活性

Fine structure and pinocytic activity of the visceral epithelium of the rat yolk sac incubated in a culture medium with or without goat antirat-placenta-IgG.

作者信息

Franke H, Goetze T, Goetze E

出版信息

Beitr Pathol. 1975;154(2):170-81. doi: 10.1016/s0005-8165(75)80210-1.

Abstract

The fine structure and pinocytic activity of the rat visceral yolk sac epithelium were examined electron microscopically after incubation in Krebs-Ringer-Phosphate solution containing either 125-I-labeled albumin or goat antirat-placenta-IgG or both compounds simultaneously. Addition of 125-I-albumin to the incubation medium stimulates the pinocytosis, whereas the addition of goat antirat-placenta-IgG, cross-reacting with the yolk sac tissue, causes a diminution of the pinocytic activity of the yolk sac epithelium. Fine structural alterations and lesions are generally noticed. Preincubation of yolk sacs in Krebs-Ringer-Phosphate solution containing goat antirat-placent-IgG and the subsequent postincubation in a new Krebs-Ringer-Phosphate medium with 125-I-albumin does not restore the original pinocytic activity of the visceral epithelial cells.

摘要

在含有125-I标记白蛋白或山羊抗大鼠胎盘IgG或这两种化合物同时存在的 Krebs-林格-磷酸盐溶液中孵育后,用电镜检查大鼠内脏卵黄囊上皮的精细结构和胞饮活性。向孵育培养基中添加125-I-白蛋白会刺激胞饮作用,而添加与卵黄囊组织发生交叉反应的山羊抗大鼠胎盘IgG会导致卵黄囊上皮胞饮活性降低。通常会注意到精细结构的改变和损伤。将卵黄囊在含有山羊抗大鼠胎盘IgG的Krebs-林格-磷酸盐溶液中预孵育,随后在含有125-I-白蛋白的新Krebs-林格-磷酸盐培养基中后孵育,并不能恢复内脏上皮细胞原来的胞饮活性。

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