Disruption of ER-mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis.

Disruption of ER-mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis.
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DOI:
10.1038/s41419-017-0022-7
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发表时间:
2018-02-28
影响因子:
9
通讯作者:
Miller CCJ
Miller CCJ
中科院分区:
生物学1区
文献类型:
--
作者:
Lau DHW;Hartopp N;Welsh NJ;Mueller S;Glennon EB;Mórotz GM;Annibali A;Gomez-Suaga P;Stoica R;Paillusson S;Miller CCJ

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额颞叶痴呆(FTD)和肌萎缩侧索硬化症(ALS)是两种相关且无法治愈的神经退行性疾病。这些疾病的特征包括受影响神经元中的病理性蛋白内含物,其中含有 TAR DNA 结合蛋白 43 (TDP-43)、源自 C9ORF72 基因的二肽重复蛋白以及肉瘤融合蛋白 (FUS),代表这些内含物中的主要组成蛋白。 C9ORF72 以及编码 TDP-43 和 FUS 的基因突变会导致家族性 FTD/ALS,这为将这些疾病的病理学和遗传学联系起来提供了证据。 FTD/ALS 中大量看似不同的生理功能受到损害。然而,许多这些受损功能是通过内质网和线粒体之间的信号传导来调节的,这激发了人们对内质网-线粒体信号传导在 FTD/ALS 疾病过程中的作用的研究。在这里,我们回顾一下这个主题的进展。
Fronto-temporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two related and incurable neurodegenerative diseases. Features of these diseases include pathological protein inclusions in affected neurons with TAR DNA-binding protein 43 (TDP-43), dipeptide repeat proteins derived from the C9ORF72 gene, and fused in sarcoma (FUS) representing major constituent proteins in these inclusions. Mutations in C9ORF72 and the genes encoding TDP-43 and FUS cause familial forms of FTD/ALS which provides evidence to link the pathology and genetics of these diseases. A large number of seemingly disparate physiological functions are damaged in FTD/ALS. However, many of these damaged functions are regulated by signalling between the endoplasmic reticulum and mitochondria, and this has stimulated investigations into the role of endoplasmic reticulum-mitochondria signalling in FTD/ALS disease processes. Here, we review progress on this topic.
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