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使用含有全氟化合物的灌注技术对生物发生途径进行的研究。

The study of biogenetic pathways using a perfusion technique containing perfluorochemicals.

作者信息

Eriksson L C, Elhammer A, Torndal U B

出版信息

Br J Exp Pathol. 1979 Apr;60(2):193-200.

Abstract

A liver perfusion system was assembled and adapted for pulse labelling studies. The perfusion medium was prepared by emulsifying perfluorotributylamine and Pluronic F 68 in a CO2 atmosphere using a sonicator. Ribosome-rich and ribosome-poor rough microsomes, smooth microsomes and Golgi membranes could be prepared from perfused livers with a good purity and recovery as from non-perfused livers. The subfractionation technique used was simple and involved slight modifications of the methods described earlier by Eriksson (1973) and Ehrenreich et al. (1973). The specific activity of NADPH-cytochrome c reductase in microsomes and of UDP-galactosyltransferase in Golgi membranes from perfused and non-perfused livers were identical. The specific activity of glucose-6-phosphatase in microsomes was slightly decreased after perfusion, but the membrane permeability barrier to glucose-6-phosphate remained intact. The granulated microsomal fractions from perfused liver had a somewhat reduced number of membrane-bound ribosomes. The system developed proved useful in studies of the synthesis and intracellular transport of albumin. The technique should also be suitable for use in studies of membrane biogenesis.

摘要

组装了一个肝脏灌注系统并对其进行改造以用于脉冲标记研究。灌注介质是通过在二氧化碳气氛中使用超声仪乳化全氟三丁胺和普朗尼克F68制备的。富含核糖体和核糖体含量低的粗面微粒体、滑面微粒体和高尔基体膜可以从灌注肝脏中制备出来,其纯度和回收率与从未灌注肝脏中制备的相当。所使用的亚分级分离技术很简单,只是对埃里克森(1973年)和埃伦赖希等人(1973年)先前描述的方法进行了轻微修改。灌注肝脏和未灌注肝脏的微粒体中NADPH - 细胞色素c还原酶以及高尔基体膜中UDP - 半乳糖基转移酶的比活性是相同的。灌注后微粒体中葡萄糖 - 6 - 磷酸酶的比活性略有下降,但对葡萄糖 - 6 - 磷酸的膜通透性屏障仍然完好。来自灌注肝脏的颗粒状微粒体部分的膜结合核糖体数量有所减少。所开发的系统在白蛋白的合成和细胞内运输研究中被证明是有用的。该技术也应该适用于膜生物发生的研究。

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