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一种多巴胺通路在帕金森病果蝇模型的进行性运动缺陷中起关键作用。

A single dopamine pathway underlies progressive locomotor deficits in a Drosophila model of Parkinson disease.

机构信息

Genetics and Physiopathology of Neurotransmission, Neurobiology Unit, CNRS, ESPCI ParisTech, 10 rue Vauquelin, 75005 Paris, France; Molecular Neurobiology of Behaviour, Johann-Friedrich-Blumenbach Institute, Georg-August-University of Goettingen, Schwann-Schleiden Research Center, Julia-Lermontowa Weg 3, 37077 Goettingen, Germany.

出版信息

Cell Rep. 2013 Nov 27;5(4):952-60. doi: 10.1016/j.celrep.2013.10.032. Epub 2013 Nov 14.

Abstract

Expression of the human Parkinson-disease-associated protein α-synuclein in all Drosophila neurons induces progressive locomotor deficits. Here, we identify a group of 15 dopaminergic neurons per hemisphere in the anterior medial region of the brain whose disruption correlates with climbing impairments in this model. These neurons selectively innervate the horizontal β and β' lobes of the mushroom bodies, and their connections to the Kenyon cells are markedly reduced when they express α-synuclein. Using selective mushroom body drivers, we show that blocking or overstimulating neuronal activity in the β' lobe, but not the β or γ lobes, significantly inhibits negative geotaxis behavior. This suggests that modulation of the mushroom body β' lobes by this dopaminergic pathway is specifically required for an efficient control of startle-induced locomotion in flies.

摘要

在所有果蝇神经元中表达人类帕金森病相关蛋白α-突触核蛋白会导致进行性运动缺陷。在这里,我们鉴定出大脑前内侧区域每侧半球有一组 15 个多巴胺能神经元,其破坏与该模型中攀爬能力受损相关。这些神经元选择性地支配蘑菇体的水平β和β'叶,当它们表达α-突触核蛋白时,它们与肯尼恩细胞的连接明显减少。使用选择性蘑菇体驱动子,我们表明,阻断或过度刺激β'叶中的神经元活性,而不是β或γ叶中的神经元活性,会显著抑制负趋地性行为。这表明,这条多巴胺能通路对蘑菇体β'叶的调制是苍蝇有效控制惊跳诱导运动所必需的。

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