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神经退行性变中的时辰化学

Chronochemistry in neurodegeneration.

作者信息

Pastore Annalisa, Adinolfi Salvatore

机构信息

Department of Clinical Neuroscience, Institute of Psychiatry, King's College London London, UK.

出版信息

Front Mol Neurosci. 2014 Mar 31;7:20. doi: 10.3389/fnmol.2014.00020. eCollection 2014.

DOI:10.3389/fnmol.2014.00020
PMID:24744696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3978368/
Abstract

The problem of distinguishing causes from effects is not a trivial one, as illustrated by the science fiction writer Isaac Asimov in a novel dedicated to an imaginary compound with surprising "chronochemistry" properties. The problem is particularly important when trying to establish the etiology of diseases. Here, we discuss how the problem reflects on our understanding of disease using two specific examples: Alzheimer's disease (AD) and Friedreich's ataxia (FRDA). We show how the fibrillar aggregates observed in AD were first denied any interest, then to assume a central focus, and to finally recess to be considered the dead-end point of the aggregation pathway. This current view is that the soluble aggregates formed along the aggregation pathway rather than the mature amyliod fiber are the causes of disease, Similarly, we illustrate how the identification of causes and and effects have been important in the study of FRDA. This disease has alternatively been considered as the consequence of oxidative stress, iron precipitation or reduction of iron-sulfur cluster protein context. We illustrate how new tools have recently been established which allow us to follow the development of the disease. We hope that this review may inspire similar studies in other scientific disciplines.

摘要

区分原因和结果并非易事,科幻作家艾萨克·阿西莫夫在一部致力于一种具有惊人“时间化学”特性的虚构化合物的小说中就说明了这一点。在试图确定疾病的病因时,这个问题尤为重要。在这里,我们通过两个具体例子讨论这个问题如何影响我们对疾病的理解:阿尔茨海默病(AD)和弗里德赖希共济失调(FRDA)。我们展示了在AD中观察到的纤维状聚集体最初是如何被忽视的,然后如何成为关注焦点,最后又退居次席,被认为是聚集途径的终点。目前的观点是,沿着聚集途径形成的可溶性聚集体而非成熟淀粉样纤维才是疾病的病因。同样,我们说明了在FRDA研究中,因果关系的确定是如何重要的。这种疾病曾被认为是氧化应激、铁沉淀或铁硫簇蛋白环境减少的结果。我们展示了最近如何建立新工具来追踪疾病的发展。我们希望这篇综述能激发其他科学学科开展类似研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b90b/3978368/c8e40b6af165/fnmol-07-00020-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b90b/3978368/f460a7867fa7/fnmol-07-00020-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b90b/3978368/c8e40b6af165/fnmol-07-00020-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b90b/3978368/f460a7867fa7/fnmol-07-00020-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b90b/3978368/c8e40b6af165/fnmol-07-00020-g002.jpg

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A new tool to determine the cellular metabolic landscape: nanotechnology to the study of Friedreich's ataxia.一种新的工具来确定细胞代谢特征:纳米技术在弗里德里希共济失调症研究中的应用。
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The time dimension of neurodegeneration: the example of Friedreich's ataxia.神经退行性变的时间维度:以弗里德赖希共济失调为例。

本文引用的文献

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Frataxin: a protein in search for a function.铁蛋白:一种寻找功能的蛋白质。
J Neurochem. 2013 Aug;126 Suppl 1:43-52. doi: 10.1111/jnc.12220.
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Biochemistry of amyloid β-protein and amyloid deposits in Alzheimer disease.阿尔茨海默病中β淀粉样蛋白和淀粉样沉积物的生物化学。
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Understanding the genetic and molecular pathogenesis of Friedreich's ataxia through animal and cellular models.通过动物和细胞模型理解弗里德里希共济失调的遗传和分子发病机制。
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The role of oxidative stress in Friedreich's ataxia.氧化应激在弗里德里希共济失调中的作用。
FEBS Lett. 2018 Mar;592(5):718-727. doi: 10.1002/1873-3468.12928. Epub 2017 Dec 20.
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A new cellular model to follow Friedreich's ataxia development in a time-resolved way.一种以时间分辨方式跟踪弗里德赖希共济失调发展的新型细胞模型。
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Overlapping binding sites of the frataxin homologue assembly factor and the heat shock protein 70 transfer factor on the Isu iron-sulfur cluster scaffold protein.铁硫簇组装因子与热休克蛋白 70 转位因子在 Isu 铁硫簇支架蛋白上的重叠结合位点。
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Dual amyloid domains promote differential functioning of the chaplin proteins during Streptomyces aerial morphogenesis.双淀粉样结构域促进了链霉菌气生形态发生过程中 Chaplin 蛋白的差异功能。
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Alzheimer's disease.阿尔茨海默病。
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