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线粒体功能障碍和 RanBP9-cofilin 通路引起的钙稳态失调。

Mitochondrial dysfunction and calcium deregulation by the RanBP9-cofilin pathway.

机构信息

1Department of Molecular Medicine, USF Health Byrd Institute, 4001 E. Fletcher Ave., Tampa, FL 33613, USA.

出版信息

FASEB J. 2013 Dec;27(12):4776-89. doi: 10.1096/fj.13-234765. Epub 2013 Aug 27.

Abstract

Mitochondrial dysfunction and synaptic damage are important features of Alzheimer's disease (AD) associated with amyloid β (Aβ) and tau. We reported previously that the scaffolding protein RanBP9, which is overall increased in brains of patients with AD and in mutant APP transgenic mice, simultaneously promotes Aβ generation and focal adhesion disruption by accelerating the endocytosis of APP and β1-integrin, respectively. Moreover, RanBP9 induces neurodegeneration in vitro and in vivo and mediates Aβ-induced neurotoxicity. Here we show in primary hippocampal neurons that RanBP9 potentiates Aβ-induced reactive oxygen species (ROS) overproduction, apoptosis, and calcium deregulation. Analyses of calcium-handling measures demonstrate that RanBP9 selectively delays the clearance of cytosolic Ca(2+) mediated by the mitochondrial calcium uniporter through a process involving the translocation of cofilin into mitochondria and oxidative mechanisms. Further, RanBP9 retards the anterograde axonal transport of mitochondria in primary neurons and decreases synaptic mitochondrial activity in brain. These data indicate that RanBP9, cofilin, and Aβ mimic and potentiate each other to produce mitochondrial dysfunction, ROS overproduction, and calcium deregulation, which leads to neurodegenerative changes reminiscent of those seen in AD.

摘要

线粒体功能障碍和突触损伤是与淀粉样蛋白 β (Aβ) 和 tau 相关的阿尔茨海默病 (AD) 的重要特征。我们之前曾报道过,支架蛋白 RanBP9 在 AD 患者的大脑和突变 APP 转基因小鼠中总体增加,它通过分别加速 APP 和 β1-整合素的内吞作用,同时促进 Aβ 的产生和焦点粘连破坏。此外,RanBP9 在体外和体内诱导神经退行性变,并介导 Aβ 诱导的神经毒性。在这里,我们在原代海马神经元中表明,RanBP9 增强了 Aβ 诱导的活性氧 (ROS) 过度产生、细胞凋亡和钙失调。钙处理措施的分析表明,RanBP9 通过将丝切蛋白转移到线粒体中和氧化机制选择性地延迟线粒体钙单向转运体介导的细胞质 Ca(2+) 的清除。此外,RanBP9 会延迟原代神经元中的顺行轴突运输,并降低大脑中的突触线粒体活性。这些数据表明,RanBP9、丝切蛋白和 Aβ 相互模仿并增强彼此的作用,导致线粒体功能障碍、ROS 过度产生和钙失调,从而产生类似于 AD 所见的神经退行性变化。

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