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异常的线粒体动力学——阿尔茨海默病的新治疗靶点?

Abnormal mitochondrial dynamics--a novel therapeutic target for Alzheimer's disease?

机构信息

Department of Pathology, Case Western Reserve University, 2103 Cornell Road, Cleveland, OH 44106, USA.

出版信息

Mol Neurobiol. 2010 Jun;41(2-3):87-96. doi: 10.1007/s12035-009-8095-7. Epub 2010 Jan 27.

DOI:10.1007/s12035-009-8095-7
PMID:20101529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3129743/
Abstract

Mitochondria are dynamic organelles that undergo continuous fission and fusion, which could affect all aspects of mitochondrial function. Mitochondrial dysfunction has been well documented in Alzheimer's disease (AD). In the past few years, emerging evidence indicates that an imbalance of mitochondrial dynamics is involved in the pathogenesis of AD. In this review, we discuss in detail the abnormal mitochondrial dynamics in AD and how such abnormal dynamics may impact mitochondrial and neuronal function and contribute to the course of disease. Based on this discussion, we propose that mitochondrial dynamics could be a potential therapeutic target for AD.

摘要

线粒体是具有动态特征的细胞器,不断经历分裂和融合,这可能会影响到线粒体功能的各个方面。线粒体功能障碍在阿尔茨海默病(AD)中已有充分的记载。在过去的几年中,新出现的证据表明,线粒体动力学的失衡与 AD 的发病机制有关。在这篇综述中,我们详细讨论了 AD 中线粒体动力学的异常,以及这种异常动力学如何影响线粒体和神经元功能,并导致疾病的发展。基于这一讨论,我们提出线粒体动力学可能是 AD 的一个潜在治疗靶点。

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本文引用的文献

1
Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondria.早老素在内质网与线粒体相关的膜中富集。
Am J Pathol. 2009 Nov;175(5):1810-6. doi: 10.2353/ajpath.2009.090219. Epub 2009 Oct 15.
2
Abnormal mitochondrial dynamics and neurodegenerative diseases.异常的线粒体动力学与神经退行性疾病。
Biochim Biophys Acta. 2010 Jan;1802(1):135-42. doi: 10.1016/j.bbadis.2009.09.013. Epub 2009 Sep 30.
3
Impaired balance of mitochondrial fission and fusion in Alzheimer's disease.阿尔茨海默病中线粒体分裂与融合的平衡受损。
J Neurosci. 2009 Jul 15;29(28):9090-103. doi: 10.1523/JNEUROSCI.1357-09.2009.
4
Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice.线粒体分裂因子Drp1对小鼠的胚胎发育和突触形成至关重要。
Nat Cell Biol. 2009 Aug;11(8):958-66. doi: 10.1038/ncb1907. Epub 2009 Jul 5.
5
Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNA.线粒体裂变的抑制有利于突变型而非野生型线粒体DNA。
Hum Mol Genet. 2009 Sep 15;18(18):3407-16. doi: 10.1093/hmg/ddp281. Epub 2009 Jun 27.
6
PGC-1{alpha} and PGC-1{beta} regulate mitochondrial density in neurons.过氧化物酶体增殖物激活受体γ辅激活因子1α(PGC-1α)和过氧化物酶体增殖物激活受体γ辅激活因子1β(PGC-1β)调节神经元中的线粒体密度。
J Biol Chem. 2009 Aug 7;284(32):21379-85. doi: 10.1074/jbc.M109.018911. Epub 2009 Jun 19.
7
Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology.PINK1基因无义突变和错义突变对线粒体功能及形态的不同影响。
Exp Neurol. 2009 Sep;219(1):266-73. doi: 10.1016/j.expneurol.2009.05.027. Epub 2009 Jun 3.
8
Mitofusins and OPA1 mediate sequential steps in mitochondrial membrane fusion.线粒体融合蛋白和 OPA1 介导线粒体膜融合的连续步骤。
Mol Biol Cell. 2009 Aug;20(15):3525-32. doi: 10.1091/mbc.e09-03-0252. Epub 2009 May 28.
9
Caspase-cleaved tau expression induces mitochondrial dysfunction in immortalized cortical neurons: implications for the pathogenesis of Alzheimer disease.半胱天冬酶切割的tau蛋白表达在永生化皮层神经元中诱导线粒体功能障碍:对阿尔茨海默病发病机制的影响。
J Biol Chem. 2009 Jul 10;284(28):18754-66. doi: 10.1074/jbc.M808908200. Epub 2009 Apr 23.
10
Amyloid beta, mitochondrial structural and functional dynamics in Alzheimer's disease.阿尔茨海默病中的β-淀粉样蛋白、线粒体结构与功能动力学
Exp Neurol. 2009 Aug;218(2):286-92. doi: 10.1016/j.expneurol.2009.03.042. Epub 2009 Apr 7.