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朊病毒蛋白在细胞形态发生过程中控制神经细胞黏附分子1的多唾液酸化。

The Prion Protein Controls Polysialylation of Neural Cell Adhesion Molecule 1 during Cellular Morphogenesis.

作者信息

Mehrabian Mohadeseh, Brethour Dylan, Wang Hansen, Xi Zhengrui, Rogaeva Ekaterina, Schmitt-Ulms Gerold

机构信息

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine & Pathobiology, University of Toronto, Toronto, Ontario, Canada.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada.

出版信息

PLoS One. 2015 Aug 19;10(8):e0133741. doi: 10.1371/journal.pone.0133741. eCollection 2015.

Abstract

Despite its multi-faceted role in neurodegenerative diseases, the physiological function of the prion protein (PrP) has remained elusive. On the basis of its evolutionary relationship to ZIP metal ion transporters, we considered that PrP may contribute to the morphogenetic reprogramming of cells underlying epithelial-to-mesenchymal transitions (EMT). Consistent with this hypothesis, PrP transcription increased more than tenfold during EMT, and stable PrP-deficient cells failed to complete EMT in a mammalian cell model. A global comparative proteomics analysis identified the neural cell adhesion molecule 1 (NCAM1) as a candidate mediator of this impairment, which led to the observation that PrP-deficient cells fail to undergo NCAM1 polysialylation during EMT. Surprisingly, this defect was caused by a perturbed transcription of the polysialyltransferase ST8SIA2 gene. Proteomics data pointed toward β-catenin as a transcriptional regulator affected in PrP-deficient cells. Indeed, pharmacological blockade or siRNA-based knockdown of β-catenin mimicked PrP-deficiency in regards to NCAM1 polysialylation. Our data established the existence of a PrP-ST8SIA2-NCAM signaling loop, merged two mature fields of investigation and offer a simple model for explaining phenotypes linked to PrP.

摘要

尽管朊病毒蛋白(PrP)在神经退行性疾病中具有多方面作用,但其生理功能仍不清楚。基于其与ZIP金属离子转运体的进化关系,我们认为PrP可能有助于上皮-间充质转化(EMT)过程中细胞的形态发生重编程。与该假设一致,在EMT过程中PrP转录增加了十多倍,并且在哺乳动物细胞模型中,稳定的PrP缺陷细胞无法完成EMT。一项全局比较蛋白质组学分析确定神经细胞黏附分子1(NCAM1)是这种损伤的候选介导因子,这导致观察到PrP缺陷细胞在EMT过程中无法进行NCAM1多聚唾液酸化。令人惊讶的是,这种缺陷是由多聚唾液酸转移酶ST8SIA2基因转录紊乱引起的。蛋白质组学数据表明β-连环蛋白是PrP缺陷细胞中受影响的转录调节因子。实际上,β-连环蛋白的药理学阻断或基于小干扰RNA的敲低在NCAM1多聚唾液酸化方面模拟了PrP缺陷。我们的数据证实了PrP-ST8SIA2-NCAM信号环的存在,融合了两个成熟的研究领域,并提供了一个简单的模型来解释与PrP相关的表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9759/4546001/76d6f59a719c/pone.0133741.g001.jpg

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