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肌张力障碍相关蛋白扭转蛋白A调节突触小泡循环。

The dystonia-associated protein torsinA modulates synaptic vesicle recycling.

作者信息

Granata Alessandra, Watson Rose, Collinson Lucy M, Schiavo Giampietro, Warner Thomas T

机构信息

Cancer Research UK London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, United Kingdom.

出版信息

J Biol Chem. 2008 Mar 21;283(12):7568-79. doi: 10.1074/jbc.M704097200. Epub 2007 Dec 31.

Abstract

The loss of a glutamic acid residue in the AAA-ATPase (ATPases associated with diverse cellular activities) torsinA is responsible for most cases of early onset autosomal dominant primary dystonia. In this study, we found that snapin, which binds SNAP-25 (synaptosome-associated protein of 25,000 Da) and enhances the association of the SNARE complex with synaptotagmin, is an interacting partner for both wild type and mutant torsinA. Snapin co-localized with endogenous torsinA on dense core granules in PC12 cells and was recruited to perinuclear inclusions containing mutant DeltaE-torsinA in neuroblastoma SH-SY5Y cells. In view of these observations, synaptic vesicle recycling was analyzed using the lipophilic dye FM1-43 and an antibody directed against an intravesicular epitope of synaptotagmin I. We found that overexpression of wild type torsinA negatively affects synaptic vesicle endocytosis. Conversely, overexpression of DeltaE-torsinA in neuroblastoma cells increases FM1-43 uptake. Knockdown of snapin and/or torsinA using small interfering RNAs had a similar inhibitory effect on the exo-endocytic process. In addition, down-regulation of torsinA causes the persistence of synaptotagmin I on the plasma membrane, which closely resembles the effect observed by the overexpression of the DeltaE-torsinA mutant. Altogether, these findings suggest that torsinA plays a role together with snapin in regulated exocytosis and that DeltaE-torsinA exerts its pathological effects through a loss of function mechanism. This may affect neuronal uptake of neurotransmitters, such as dopamine, playing a role in the development of dystonic movements.

摘要

AAA-ATP酶(与多种细胞活动相关的ATP酶)扭转蛋白A中谷氨酸残基的缺失是大多数早发性常染色体显性原发性肌张力障碍病例的病因。在本研究中,我们发现与SNAP-25(25000 Da的突触体相关蛋白)结合并增强SNARE复合体与突触结合蛋白结合的小突触泡蛋白是野生型和突变型扭转蛋白A的相互作用伴侣。小突触泡蛋白与PC12细胞致密核心颗粒上的内源性扭转蛋白A共定位,并在神经母细胞瘤SH-SY5Y细胞中被募集到含有突变体DeltaE-扭转蛋白A的核周包涵体中。基于这些观察结果,我们使用亲脂性染料FM1-43和针对突触结合蛋白I囊泡内表位的抗体分析了突触小泡循环。我们发现野生型扭转蛋白A的过表达对突触小泡内吞作用有负面影响。相反,神经母细胞瘤细胞中DeltaE-扭转蛋白A的过表达增加了FM1-43的摄取。使用小干扰RNA敲低小突触泡蛋白和/或扭转蛋白A对胞吐-内吞过程有类似的抑制作用。此外,扭转蛋白A的下调导致突触结合蛋白I在质膜上持续存在,这与DeltaE-扭转蛋白A突变体过表达所观察到的效应非常相似。总之,这些发现表明扭转蛋白A与小突触泡蛋白在调节性胞吐作用中共同发挥作用,并且DeltaE-扭转蛋白A通过功能丧失机制发挥其病理作用。这可能会影响神经元对神经递质(如多巴胺)的摄取,在肌张力障碍性运动的发展中起作用。

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