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朊病毒蛋白可保护人类神经元免受Bax介导的细胞凋亡。

Prion protein protects human neurons against Bax-mediated apoptosis.

作者信息

Bounhar Y, Zhang Y, Goodyer C G, LeBlanc A

机构信息

Department of Neurology and Neurosurgery, McGill University, Montréal, PQ, H3A 2T5 Canada.

出版信息

J Biol Chem. 2001 Oct 19;276(42):39145-9. doi: 10.1074/jbc.C100443200. Epub 2001 Aug 24.

Abstract

The function of the cellular prion protein (PrP) is still poorly understood. We present here an unprecedented role for PrP against Bax-mediated neuronal apoptosis and show that PrP potently inhibits Bax-induced cell death in human primary neurons. Deletion of four octapeptide repeats of PrP (PrPDeltaOR) and familial D178N and T183A PrP mutations completely or partially eliminate the neuroprotective effect of PrP. PrP remains anti-apoptotic despite truncation of the glycosylphosphatidylinositol (GPI) anchor signal peptide, indicating that the neuroprotective form of PrP does not require the abundant cell surface GPI-anchored PrP. Our results implicate PrP as a potent and novel anti-apoptotic protein against Bax-mediated cell death.

摘要

细胞朊蛋白(PrP)的功能仍知之甚少。我们在此揭示了PrP在对抗Bax介导的神经元凋亡方面前所未有的作用,并表明PrP能有效抑制人原代神经元中Bax诱导的细胞死亡。PrP的四个八肽重复序列缺失(PrPDeltaOR)以及家族性D178N和T183A PrP突变完全或部分消除了PrP的神经保护作用。尽管糖基磷脂酰肌醇(GPI)锚定信号肽被截断,PrP仍具有抗凋亡作用,这表明PrP的神经保护形式并不需要大量细胞表面GPI锚定的PrP。我们的结果表明PrP是一种针对Bax介导的细胞死亡的有效且新型的抗凋亡蛋白。

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