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α-突触核蛋白破坏多巴胺稳态导致秀丽隐杆线虫多巴胺能神经元变性。

Alpha-synuclein disrupted dopamine homeostasis leads to dopaminergic neuron degeneration in Caenorhabditis elegans.

机构信息

Department of Pharmacology, School of Medicine, Case Western Reserve University, Cleveland, Ohio, United States of America.

出版信息

PLoS One. 2010 Feb 19;5(2):e9312. doi: 10.1371/journal.pone.0009312.

Abstract

Disruption of dopamine homeostasis may lead to dopaminergic neuron degeneration, a proposed explanation for the specific vulnerability of dopaminergic neurons in Parkinson's disease. While expression of human alpha-synuclein in C. elegans results in dopaminergic neuron degeneration, the effects of alpha-synuclein on dopamine homeostasis and its contribution to dopaminergic neuron degeneration in C. elegans have not been reported. Here, we examined the effects of alpha-synuclein overexpression on worm dopamine homeostasis. We found that alpha-synuclein expression results in upregulation of dopamine synthesis and content, and redistribution of dopaminergic synaptic vesicles, which significantly contribute to dopaminergic neuron degeneration. These results provide in vivo evidence supporting a critical role for dopamine homeostasis in supporting dopaminergic neuron integrity.

摘要

多巴胺稳态的破坏可能导致多巴胺能神经元变性,这是帕金森病中多巴胺能神经元易损性的一个假设解释。虽然人α-突触核蛋白在秀丽隐杆线虫中的表达导致多巴胺能神经元变性,但α-突触核蛋白对多巴胺稳态的影响及其在秀丽隐杆线虫中对多巴胺能神经元变性的贡献尚未报道。在这里,我们研究了α-突触核蛋白过表达对蠕虫多巴胺稳态的影响。我们发现,α-突触核蛋白的表达导致多巴胺合成和含量的上调,以及多巴胺能突触小泡的重新分布,这对多巴胺能神经元变性有重要贡献。这些结果提供了体内证据,支持多巴胺稳态在支持多巴胺能神经元完整性方面的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5206/2824852/5aa40ec4039c/pone.0009312.g001.jpg

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