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通过细胞融合对人纤溶酶原激活剂进行调节和图谱绘制。

Modulation and mapping of a human plasminogen activator by cell fusion.

作者信息

Kucherlapati R, Tepper R, Granelli-Piperno A, Reich E

出版信息

Cell. 1978 Dec;15(4):1331-40. doi: 10.1016/0092-8674(78)90058-2.

Abstract

Neoplastic cells, transformed cells and some normal mammalian cells secrete large amounts of plasminogen activator (PA), an arginine-specific protease which converts plasminogen to plasmin. To study the regulation of PA, we have obtained two classes of mouse-human somatic cell hybrids. PG19, a mouse PA+ cell line, was fused with C32 (human PA+) or human diploid fibroblasts (PA-). All hybrids secreted PA. Human- and mouse-specific forms of PA were distinguished in these hybrids by electrophoretic methods. While all hybrids produced the murine PA, many produced the human PA and some did not. All hybrids which produced human PA had chromosome 6 in common. The absence of each of the other human chromosomes did not affect PA expression, while the absence of chromosome 6 correlated with the lack of human PA. We conclude that chromosome 6 carries the structural gene for human PA. These experiments also show that the fusion of mouse PA+ cells with human PA- cells results in the activation of the human PA gene.

摘要

肿瘤细胞、转化细胞和一些正常哺乳动物细胞会分泌大量的纤溶酶原激活物(PA),这是一种精氨酸特异性蛋白酶,可将纤溶酶原转化为纤溶酶。为了研究PA的调控机制,我们获得了两类小鼠 - 人类体细胞杂种。PG19是一种小鼠PA+细胞系,它与C32(人类PA+)或人类二倍体成纤维细胞(PA-)进行了融合。所有杂种都分泌PA。通过电泳方法在这些杂种中区分出了人类和小鼠特异性形式的PA。虽然所有杂种都产生小鼠PA,但许多杂种产生人类PA,有些则不产生。所有产生人类PA的杂种都共同拥有6号染色体。其他人类染色体的缺失并不影响PA的表达,而6号染色体的缺失与人类PA的缺乏相关。我们得出结论,6号染色体携带人类PA的结构基因。这些实验还表明,小鼠PA+细胞与人类PA-细胞的融合导致了人类PA基因的激活。

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