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高水平的细胞朊蛋白可改善星形胶质细胞的发育。

High levels of cellular prion protein improve astrocyte development.

机构信息

International Research Center, A.C. Camargo Hospital, São Paulo, Brazil.

出版信息

FEBS Lett. 2013 Jan 16;587(2):238-44. doi: 10.1016/j.febslet.2012.11.032. Epub 2012 Dec 10.

Abstract

Prion protein (PrP(C)) has neuroprotective functions and herein we demonstrate that astrocytes from PrP(C)-over-expressing mice are more resistant to induced cell death than wild-type astrocytes. The Stress-Inducible-Protein 1 (STI1), a PrP(C) ligand, prevents cell death in both wild-type and PrP(C)-over-expressing astrocytes through the activation of protein-kinase-A. Cultured embryonic astrocytes and brain extracts from PrP(C)-over-expressing mice show higher glial fibrillary acidic protein expression and reduced vimentin and nestin levels when compared to wild-type astrocytes, suggesting faster astrocyte maturation in the former mice. Our data indicate that PrP(C) levels modulate astrocyte development, and that PrP(C)-STI1 interaction contributes to protect against astrocyte death.

摘要

朊病毒蛋白(PrP(C))具有神经保护功能,本文证明过表达 PrP(C)的小鼠星形胶质细胞比野生型星形胶质细胞更能抵抗诱导的细胞死亡。应激诱导蛋白 1(STI1)是 PrP(C)的配体,可通过激活蛋白激酶 A 来防止野生型和过表达 PrP(C)的星形胶质细胞发生细胞死亡。与野生型星形胶质细胞相比,过表达 PrP(C)的小鼠胚胎星形胶质细胞和脑提取物中神经胶质纤维酸性蛋白的表达更高,波形蛋白和巢蛋白的水平更低,这表明前者的星形胶质细胞成熟更快。我们的数据表明,PrP(C)水平调节星形胶质细胞的发育,而 PrP(C)-STI1 相互作用有助于防止星形胶质细胞死亡。

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