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Modification of γ-secretase by nitrosative stress links neuronal ageing to sporadic Alzheimers disease

机译:亚硝化应激对γ-分泌酶的修饰将神经元衰老与偶发的阿尔茨海默氏病联系起来

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摘要

Inherited familial Alzheimer's disease (AD) is characterized by small increases in the ratio of Aβ42 versus Aβ40 peptide which is thought to drive the amyloid plaque formation in the brain of these patients. Little is known however whether ageing, the major risk factor for sporadic AD, affects amyloid beta-peptide (Aβ) generation as well. Here we demonstrate that the secretion of Aβ is enhanced in an in vitro model of neuronal ageing, correlating with an increase in γ-secretase complex formation. Moreover we found that peroxynitrite (ONOO), produced by the reaction of superoxide anion with nitric oxide, promoted the nitrotyrosination of presenilin 1 (PS1), the catalytic subunit of γ-secretase. This was associated with an increased association of the two PS1 fragments, PS1-CTF and PS1-NTF, which constitute the active catalytic centre. Furthermore, we found that peroxynitrite shifted the production of Aβ towards Aβ42 and increased the Aβ42/Aβ40 ratio. Our work identifies nitrosative stress as a potential mechanistic link between ageing and AD.
机译:遗传性家族性阿尔茨海默氏病(AD)的特征是Aβ42与Aβ40肽的比例略有增加,这被认为可驱动这些患者大脑中的淀粉样斑块形成。然而,对于偶发性AD的主要危险因素,衰老是否也会影响淀粉样β肽(Aβ)的产生还知之甚少。在这里,我们证明神经元衰老的体外模型中Aβ的分泌增加,与γ-分泌酶复合物形成的增加相关。此外,我们发现由超氧阴离子与一氧化氮反应产生的过氧亚硝酸盐(ONOO -)促进了早老素1(PS1)的γ-酪氨酸化,这是γ-分泌酶的催化亚基。这与构成活性催化中心的两个PS1片段PS1-CTF和PS1-NTF的缔合增加有关。此外,我们发现过氧亚硝酸盐将Aβ的产生移向Aβ42并增加了Aβ42/Aβ40的比率。我们的工作将亚硝化应力识别为衰老和AD之间的潜在机制联系。

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