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缺乏朊蛋白的小鼠对羊瘙痒病具有抵抗力。

Mice devoid of PrP are resistant to scrapie.

作者信息

Büeler H, Aguzzi A, Sailer A, Greiner R A, Autenried P, Aguet M, Weissmann C

机构信息

Institut für Molekularbiologie I, Universität Zürich, Switzerland.

出版信息

Cell. 1993 Jul 2;73(7):1339-47. doi: 10.1016/0092-8674(93)90360-3.

Abstract

S.B. Prusiner proposed that the infectious agent of scraple, the prion, is PrPSc, a modified form of the normal host protein PrPC. Prn-p0/0 mice devoid of PrPC showed normal development and behavior. When inoculated with mouse scrapie prions, they remained free of scrapie symptoms for at least 13 months while wild-type controls all died within 6 months. Surprisingly, heterozygous Prn-p0/+ mice also showed enhanced resistance to scrapie. After introduction of Syrian hamster PrP transgenes, Prn-p0/0 mice became highly susceptible to hamster but not to mouse prions. These experiments show that PrPC, possibly at close to normal levels, is required for the usual susceptibility to scrapie and that lack of homology between incoming prions and the host's PrP genes retards disease.

摘要

S.B.普鲁辛纳提出,羊瘙痒症的感染因子朊病毒是PrPSc,即正常宿主蛋白PrPC的一种修饰形式。缺乏PrPC的Prn-p0/0小鼠表现出正常的发育和行为。当接种小鼠瘙痒症朊病毒时,它们至少13个月没有出现瘙痒症症状,而野生型对照在6个月内全部死亡。令人惊讶的是,杂合子Prn-p0/+小鼠对瘙痒症也表现出增强的抵抗力。引入叙利亚仓鼠PrP转基因后,Prn-p0/0小鼠对仓鼠朊病毒变得高度易感,但对小鼠朊病毒不易感。这些实验表明,PrPC可能处于接近正常的水平,是对瘙痒症正常易感性所必需的,并且传入的朊病毒与宿主的PrP基因之间缺乏同源性会延缓疾病的发生。

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