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阿尔茨海默病神经元中线粒体裂变蛋白 Drp1 与过度磷酸化 tau 之间的异常相互作用:对线粒体功能障碍和神经元损伤的影响。

Abnormal interaction between the mitochondrial fission protein Drp1 and hyperphosphorylated tau in Alzheimer's disease neurons: implications for mitochondrial dysfunction and neuronal damage.

机构信息

Neurogenetics Laboratory, Neuroscience Division, Oregon National Primate Research Center, West Campus, Oregon Health and Science University, Beaverton, OR 97006, USA.

出版信息

Hum Mol Genet. 2012 Jun 1;21(11):2538-47. doi: 10.1093/hmg/dds072. Epub 2012 Feb 24.

DOI:10.1093/hmg/dds072
PMID:22367970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3349426/
Abstract

We recently reported increased mitochondrial fission and decreased fusion, increased amyloid beta (Aβ) interaction with the mitochondrial fission protein Drp1, increased mitochondrial fragmentation, impaired axonal transport of mitochondria and synaptic degeneration in neurons affected by AD. In the present study, we extended our previous investigations to determine whether phosphorylated tau interacts with Drp1 and to elucidate mitochondrial damage in the progression of AD. We also investigated GTPase activity, which is critical for mitochondrial fragmentation, in postmortem brain tissues from patients with AD and brain tissues from APP, APP/PS1 and 3XTg.AD mice. Using co-immunoprecipitation and immunofluorescence analyses, for the first time, we demonstrated the physical interaction between phosphorylated tau and Drp1. Mitochondrial fission-linked GTPase activity was significantly elevated in the postmortem frontal cortex tissues from AD patients and cortical tissues from APP, APP/PS1 and 3XTg.AD mice. On the basis of these findings, we conclude that Drp1 interacts with Aβ and phosphorylated tau, likely leading to excessive mitochondrial fragmentation, and mitochondrial and synaptic deficiencies, ultimately possibly leading to neuronal damage and cognitive decline. Treatment designed to reduce the expression of Drp1, Aβ and/or phosphorylated tau may decrease the interaction between Drp1 and phosphorylated tau and the interaction between Drp1 and Aβ, conferring protection to neurons from toxic insults of excessive Drp1, Aβ and/or phosphorylated tau.

摘要

我们最近报道了 AD 神经元中线粒体裂变增加和融合减少、β 淀粉样蛋白 (Aβ) 与线粒体裂变蛋白 Drp1 相互作用增加、线粒体碎片化增加、线粒体在轴突中的运输受损以及突触退化。在本研究中,我们扩展了之前的研究,以确定磷酸化 tau 是否与 Drp1 相互作用,并阐明 AD 进展中的线粒体损伤。我们还研究了 GTPase 活性,它对线粒体碎片化至关重要,在 AD 患者的死后脑组织和 APP、APP/PS1 和 3XTg.AD 小鼠的脑组织中进行了研究。通过共免疫沉淀和免疫荧光分析,我们首次证明了磷酸化 tau 与 Drp1 之间的物理相互作用。AD 患者死后额皮质组织和 APP、APP/PS1 和 3XTg.AD 小鼠皮质组织中线粒体裂变相关 GTPase 活性显著升高。基于这些发现,我们得出结论,Drp1 与 Aβ 和磷酸化 tau 相互作用,可能导致过度的线粒体碎片化以及线粒体和突触缺陷,最终可能导致神经元损伤和认知能力下降。旨在降低 Drp1、Aβ 和/或磷酸化 tau 表达的治疗方法可能会减少 Drp1 和磷酸化 tau 之间以及 Drp1 和 Aβ 之间的相互作用,从而为神经元提供免受过度 Drp1、Aβ 和/或磷酸化 tau 毒性侵害的保护。

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Biochim Biophys Acta. 2012 Jun;1822(6):862-74. doi: 10.1016/j.bbadis.2012.02.017. Epub 2012 Feb 23.
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Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria.肌萎缩侧索硬化症相关突变 VAPBP56S 破坏钙稳态,扰乱线粒体的轴突运输。
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Mitochondrial dynamics and bioenergetic dysfunction is associated with synaptic alterations in mutant SOD1 motor neurons.线粒体动态和生物能量功能障碍与突变 SOD1 运动神经元突触改变有关。
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Mutant huntingtin's interaction with mitochondrial protein Drp1 impairs mitochondrial biogenesis and causes defective axonal transport and synaptic degeneration in Huntington's disease.突变型亨廷顿蛋白与线粒体蛋白 Drp1 的相互作用会损害线粒体生物发生,导致亨廷顿病中的轴突运输缺陷和突触退化。
Hum Mol Genet. 2012 Jan 15;21(2):406-20. doi: 10.1093/hmg/ddr475. Epub 2011 Oct 13.
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Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease.阿尔茨海默病小鼠模型中线粒体生物发生受损、线粒体轴突运输缺陷、线粒体动态异常和突触退化。
Hum Mol Genet. 2011 Dec 1;20(23):4515-29. doi: 10.1093/hmg/ddr381. Epub 2011 Aug 25.
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Abnormal tau, mitochondrial dysfunction, impaired axonal transport of mitochondria, and synaptic deprivation in Alzheimer's disease.阿尔茨海默病中的异常tau、线粒体功能障碍、线粒体轴突运输受损和突触缺失。
Brain Res. 2011 Sep 30;1415:136-48. doi: 10.1016/j.brainres.2011.07.052. Epub 2011 Jul 31.
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