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肌萎缩侧索硬化症(ALS)相关 VAPB-P56S 包含物代表内质网质量控制区室。

Amyotrophic lateral sclerosis (ALS)-associated VAPB-P56S inclusions represent an ER quality control compartment.

机构信息

Department of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

Acta Neuropathol Commun. 2013 Jun 12;1:24. doi: 10.1186/2051-5960-1-24.

Abstract

BACKGROUND

Protein aggregation and the formation of intracellular inclusions are a central feature of many neurodegenerative disorders, but precise knowledge about their pathogenic role is lacking in most instances. Here we have characterized inclusions formed in transgenic mice carrying the P56S mutant form of VAPB that causes various motor neuron syndromes including ALS8.

RESULTS

Inclusions in motor neurons of VAPB-P56S transgenic mice are characterized by the presence of smooth ER-like tubular profiles, and are immunoreactive for factors that operate in the ER associated degradation (ERAD) pathway, including p97/VCP, Derlin-1, and the ER membrane chaperone BAP31. The presence of these inclusions does not correlate with signs of axonal and neuronal degeneration, and axotomy leads to their gradual disappearance, indicating that they represent reversible structures. Inhibition of the proteasome and knockdown of the ER membrane chaperone BAP31 increased the size of mutant VAPB inclusions in primary neuron cultures, while knockdown of TEB4, an ERAD ubiquitin-protein ligase, reduced their size. Mutant VAPB did not codistribute with mutant forms of seipin that are associated with an autosomal dominant motor neuron disease, and accumulate in a protective ER derived compartment termed ERPO (ER protective organelle) in neurons.

CONCLUSIONS

The data indicate that the VAPB-P56S inclusions represent a novel reversible ER quality control compartment that is formed when the amount of mutant VAPB exceeds the capacity of the ERAD pathway and that isolates misfolded and aggregated VAPB from the rest of the ER. The presence of this quality control compartment reveals an additional level of flexibility of neurons to cope with misfolded protein stress in the ER.

摘要

背景

蛋白质聚集和细胞内包涵体的形成是许多神经退行性疾病的一个核心特征,但在大多数情况下,我们对它们的致病作用知之甚少。在这里,我们对携带 P56S 突变形式 VAPB 的转基因小鼠中形成的包涵体进行了特征描述,该突变形式会导致包括 ALS8 在内的各种运动神经元综合征。

结果

VAPB-P56S 转基因小鼠运动神经元中的包涵体的特征是存在光滑的内质网样管状结构,并对在 ER 相关降解 (ERAD) 途径中起作用的因子具有免疫反应性,包括 p97/VCP、Derlin-1 和内质网膜伴侣 BAP31。这些包涵体的存在与轴突和神经元变性的迹象无关,轴突切断导致它们逐渐消失,表明它们是可逆的结构。蛋白酶体的抑制和内质网膜伴侣 BAP31 的敲低增加了原代神经元培养物中突变 VAPB 包涵体的大小,而 ERAD 泛素蛋白连接酶 TEB4 的敲低则减小了它们的大小。突变 VAPB 与常染色体显性运动神经元疾病相关的突变 seipin 形式不同,并且在神经元中积累在一种称为 ERPO(内质网保护细胞器)的保护性内质网衍生隔室中。

结论

数据表明,VAPB-P56S 包涵体代表一种新型的可逆内质网质量控制隔室,当突变 VAPB 的量超过 ERAD 途径的容量时形成,并且将错误折叠和聚集的 VAPB 与内质网的其余部分隔离开来。这种质量控制隔室的存在揭示了神经元应对内质网中错误折叠蛋白应激的额外灵活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d524/3893532/757e7e134ef3/2051-5960-1-24-1.jpg

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