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在阿尔茨海默病早期发病机制中,β淀粉样蛋白通过线粒体融合蛋白产生的线粒体毒性作用

Mitochondrial toxic effects of Aβ through mitofusins in the early pathogenesis of Alzheimer's disease.

作者信息

Wu Zhaofei, Zhu Yushan, Cao Xingshui, Sun Shufeng, Zhao Baolu

机构信息

State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Chaoyang District, Beijing, 100101, China.

出版信息

Mol Neurobiol. 2014 Dec;50(3):986-96. doi: 10.1007/s12035-014-8675-z. Epub 2014 Apr 8.

Abstract

Mitochondrial dysfunction has been implicated in the pathogenesis of Alzheimer's disease (AD). However, it is obscure how amyloid-beta (Aβ) can impair mitochondria in the early stage of AD pathology. Using PrP-hAPP/hPS1 double-transgenic AD mouse model, we find that abnormal mitochondrial morphology and damaged mitochondrial structure in hippocampal neurons appear in the early stage of AD-like disease development. We also find consistent mitochondrial abnormalities in the SH-SY5Y cells, which express amyloid precursor protein (APP) Swedish mutation (APPsw) and have been used as a cell model of the early-onset AD. Significant changes of mitofusin GTPases (Mfn1 and Mfn2) were detected both in the PrP-hAPP/hPS1 brains and SH-SY5Y cells. Moreover, our results show that Aβ accumulation in neurons of PrP-hAPP/hPS1 mice can affect the neurogenesis prior to plaque formation. These findings suggest that mitochondrial impairment is a very early event in AD pathogenesis and abnormal expression of Mfn1 and Mfn2 caused by excessive intracellular Aβ is the possible molecular mechanism. Interestingly, L-theanine has significant effects on regulating mitochondrial fusion proteins in SH-SY5Y (APPsw) cells. Overall, our results not only suggest a new early mechanism of AD pathogenesis but also propose a preventive candidate, L-theanine, for the treatment of AD.

摘要

线粒体功能障碍与阿尔茨海默病(AD)的发病机制有关。然而,在AD病理早期,β淀粉样蛋白(Aβ)如何损害线粒体尚不清楚。利用PrP-hAPP/hPS1双转基因AD小鼠模型,我们发现在类AD疾病发展的早期阶段,海马神经元中线粒体形态异常和线粒体结构受损。我们还在表达淀粉样前体蛋白(APP)瑞典突变体(APPsw)且已被用作早发性AD细胞模型的SH-SY5Y细胞中发现了一致的线粒体异常。在PrP-hAPP/hPS1小鼠脑和SH-SY5Y细胞中均检测到线粒体融合GTP酶(Mfn1和Mfn2)的显著变化。此外,我们的结果表明,PrP-hAPP/hPS1小鼠神经元中的Aβ积累可在斑块形成之前影响神经发生。这些发现表明,线粒体损伤是AD发病机制中非常早期的事件,细胞内Aβ过量导致的Mfn1和Mfn2异常表达是可能的分子机制。有趣的是,L-茶氨酸对调节SH-SY5Y(APPsw)细胞中的线粒体融合蛋白有显著作用。总体而言,我们的结果不仅提出了AD发病机制的一种新的早期机制,还提出了一种用于治疗AD的预防性候选物L-茶氨酸。

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