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脯氨酰寡肽酶调控小鼠黑质纹状体通路多巴胺转运体的磷酸化。

Prolyl Oligopeptidase Regulates Dopamine Transporter Phosphorylation in the Nigrostriatal Pathway of Mouse.

机构信息

Division of Pharmacology and Pharmacotherapy, University of Helsinki, Viikinkaari 5E, P.O. Box 56, 00014, Helsinki, Finland.

Institute of Biotechnology, University of Helsinki, Viikinkaari 5D, P.O. Box 56, 00014, Helsinki, Finland.

出版信息

Mol Neurobiol. 2018 Jan;55(1):470-482. doi: 10.1007/s12035-016-0339-8. Epub 2016 Dec 13.

Abstract

Alpha-synuclein is the main component of Lewy bodies, a histopathological finding of Parkinson's disease. Prolyl oligopeptidase (PREP) is a serine protease that binds to α-synuclein and accelerates its aggregation in vitro. PREP enzyme inhibitors have been shown to block the α-synuclein aggregation process in vitro and in cellular models, and also to enhance the clearance of α-synuclein aggregates in transgenic mouse models. Moreover, PREP inhibitors have induced alterations in dopamine and metabolite levels, and dopamine transporter immunoreactivity in the nigrostriatal tissue. In this study, we characterized the role of PREP in the nigrostriatal dopaminergic and GABAergic systems of wild-type C57Bl/6 and PREP knockout mice, and the effects of PREP overexpression on these systems. Extracellular concentrations of dopamine and protein levels of phosphorylated dopamine transporter were increased and dopamine reuptake was decreased in the striatum of PREP knockout mice, suggesting increased internalization of dopamine transporter from the presynaptic membrane. Furthermore, PREP overexpression increased the level of dopamine transporters in the nigrostriatal tissue but decreased phosphorylated dopamine transporters in the striatum in wild-type mice. Our results suggest that PREP regulates the function of dopamine transporter, possibly by controlling the phosphorylation and transport of dopamine transporter into the striatum or synaptic membrane.

摘要

α-突触核蛋白是路易体的主要成分,路易体是帕金森病的一种组织病理学发现。脯氨酰寡肽酶(PREP)是一种丝氨酸蛋白酶,可与α-突触核蛋白结合,并在体外加速其聚集。研究表明,PREP 酶抑制剂可阻断α-突触核蛋白在体外和细胞模型中的聚集过程,并增强转基因小鼠模型中α-突触核蛋白聚集体的清除。此外,PREP 抑制剂还可诱导黑质纹状体组织中多巴胺和代谢物水平以及多巴胺转运体免疫反应的改变。在这项研究中,我们研究了 PREP 在野生型 C57Bl/6 和 PREP 敲除小鼠的黑质纹状体多巴胺能和 GABA 能系统中的作用,以及 PREP 过表达对这些系统的影响。PREP 敲除小鼠纹状体中多巴胺的细胞外浓度和磷酸化多巴胺转运体的蛋白水平增加,多巴胺再摄取减少,表明多巴胺转运体从突触前膜内化增加。此外,PREP 过表达增加了野生型小鼠黑质纹状体组织中多巴胺转运体的水平,但降低了纹状体中磷酸化多巴胺转运体的水平。我们的结果表明,PREP 调节多巴胺转运体的功能,可能通过控制多巴胺转运体进入纹状体或突触膜的磷酸化和转运来实现。

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