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从部分肝切除大鼠的血浆中纯化肝脏DNA合成促进剂。

Purification of a liver DNA-synthesis promoter from plasma of partially hepatectomized rats.

作者信息

Díaz-Gil J J, Escartín P, García-Cañero R, Trilla C, Veloso J J, Sánchez G, Moreno-Caparrós A, Enrique de Salamanca C, Lozano R, Gavilanes J G

出版信息

Biochem J. 1986 Apr 1;235(1):49-55. doi: 10.1042/bj2350049.

Abstract

A protein was isolated from plasma of partially (70%) hepatectomized rats that, injected in mice, increases the uptake of [3H]thymidine by liver DNA by 200-300% over that by injected control saline. The purification procedure consists essentially of three chromatography steps, employing Sephadex G-75, DEAE-cellulose and hydroxyapatite. The hepatic promoter (HP) preparation shows a single band in SDS/polyacrylamide (15%)-gel electrophoresis (silver stained), with an Mr of 64 000; its activity is suppressed by trypsin or pepsin and is unaffected by deoxyribonuclease or ribonuclease. On injection into mice (150 ng/mouse), it increases the mitotic index of the liver. It shows organ-specificity, acting on liver but not on spleen, kidney, lung or brain. In primary liver cultures, it produces an increase in uptake of [3H]thymidine into DNA in the range 1-10 ng/ml. In this system in vitro, it increases the uptake of 22Na+ immediately after addition.

摘要

从部分(70%)肝切除大鼠的血浆中分离出一种蛋白质,将其注射到小鼠体内后,肝脏DNA对[3H]胸腺嘧啶核苷的摄取量比注射对照生理盐水的小鼠增加200% - 300%。纯化过程主要包括三个色谱步骤,使用葡聚糖凝胶G - 75、二乙氨基乙基纤维素和羟基磷灰石。肝启动子(HP)制剂在SDS/聚丙烯酰胺(15%)凝胶电泳(银染)中显示出一条带,分子量为64000;其活性被胰蛋白酶或胃蛋白酶抑制,不受脱氧核糖核酸酶或核糖核酸酶影响。注射到小鼠体内(150 ng/小鼠)后,它会增加肝脏的有丝分裂指数。它具有器官特异性,作用于肝脏,而不作用于脾脏、肾脏、肺或大脑。在原代肝细胞培养中,它在1 - 10 ng/ml的范围内使DNA对[3H]胸腺嘧啶核苷的摄取增加。在这个体外系统中,添加后它会立即增加22Na+的摄取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6df9/1146647/fed6ddac3493/biochemj00282-0058-a.jpg

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