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尼曼-匹克 C1 型缺陷神经元中兴奋性和抑制性突触囊泡转运的缺陷。

Defects of synaptic vesicle turnover at excitatory and inhibitory synapses in Niemann-Pick C1-deficient neurons.

机构信息

Department of Neurobiology, Institute of Neuroscience, Zhejiang University School of Medicine, Hangzhou, Zhejiang, PR China.

出版信息

Neuroscience. 2010 May 19;167(3):608-20. doi: 10.1016/j.neuroscience.2010.02.033. Epub 2010 Feb 16.

Abstract

Niemann-Pick disease type C (NPC) is a progressive neurodegenerative disorder characterized by accumulation of free cholesterol in late endosomes/lysosomes. The pathological basis for the disease is poorly understood. In the present study, electrophysiological and fluorescent dye studies were applied to examine neuron-specific functions of Niemann-Pick disease type C1 (NPC1) and to determine whether excitatory and inhibitory synapses are differentially impaired by NPC1 deficiency. Densities of spines and postsynaptic receptor clusters were not affected by NPC1 deficiency over the period examined. However, drastic defects on exocytosis were found both in glutamatergic and GABAergic synapses. The defects were caused in part by a delay in the time required for replacement of excytosed vesicles with new fusion-competent ones. Moreover, we found that the delay of synaptic vesicle turnover was longer in inhibitory synapses (>3 s) than in excitatory synapses (<0.2 s). These defects may be early indicators, and could provide a potential explanation for key features of the disease, such as dystonia and seizures.

摘要

尼曼-匹克病 C 型(NPC)是一种进行性神经退行性疾病,其特征是晚期内体/溶酶体中游离胆固醇的积累。该疾病的病理基础尚不清楚。在本研究中,应用电生理和荧光染料研究来检查 NPC1 特异性神经元功能,并确定兴奋性和抑制性突触是否因 NPC1 缺乏而受到不同程度的损害。在研究期间,NPC1 缺乏并未影响棘密度和突触后受体簇。然而,在谷氨酸能和 GABA 能突触中均发现了胞吐作用的严重缺陷。该缺陷部分是由于替换胞吐的囊泡与新的融合相容囊泡之间所需的时间延迟所致。此外,我们发现抑制性突触(>3 s)中突触囊泡周转率的延迟时间长于兴奋性突触(<0.2 s)。这些缺陷可能是早期指标,并为疾病的关键特征(如肌张力障碍和癫痫发作)提供了潜在的解释。

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