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神经元突触小泡蛋白在发育中和成熟的果蝇光感受器中的不同功能。

Distinct functions of neuronal synaptobrevin in developing and mature fly photoreceptors.

作者信息

Rister Jens, Heisenberg Martin

机构信息

Lehrstuhl für Genetik und Neurobiologie der Universität Würzburg, Biozentrum Am Hubland, D-97074 Würzburg, Germany.

出版信息

J Neurobiol. 2006 Oct;66(12):1271-84. doi: 10.1002/neu.20284.

DOI:10.1002/neu.20284
PMID:16967508
Abstract

Neuronal synaptobrevin (n-Syb, alias VAMP2), a synaptic vesicle membrane protein with a central role in neurotransmission, is specifically cleaved by the light chain of tetanus neurotoxin (TNT) that is known to reliably block neuroexocytosis. Here, we study fly photoreceptors transmitting continuous, graded signals to first order interneurons in the lamina, and report consequences of targeted expression of TNT in these cells using the UAS/GAL4 driver/effector system. Expressing the toxin throughout photoreceptor development causes developmental, electrophysiological, and behavioral defects. These can be differentiated by confining toxin expression to shorter developmental periods. Applying a method for controlled temporal and spatial TNT expression, we found that in the early pupa it impaired the development of the retina; in the midpupa, during synapse formation TNT caused a severe hypoplasia of the lamina that persisted into adulthood and left the photoreceptor-interneuron synapses of the lamina without function. Finally, during adulthood TNT neither blocks synaptic transmission in photoreceptors nor depletes the cells of n-Syb. Our study suggests a novel, cell type-specific function of n-Syb in synaptogenesis and it distinguishes between two synapse types: TNT resistant and TNT sensitive ones. These results need to be taken into account if TNT is used for neural circuit analysis.

摘要

神经元突触小泡蛋白(n-Syb,别名VAMP2)是一种在神经传递中起核心作用的突触小泡膜蛋白,它会被破伤风神经毒素(TNT)的轻链特异性切割,而破伤风神经毒素已知能可靠地阻断神经胞吐作用。在此,我们研究了向神经节层中的一级中间神经元传递连续分级信号的果蝇光感受器,并报告了使用UAS/GAL4驱动/效应系统在这些细胞中靶向表达TNT的后果。在整个光感受器发育过程中表达毒素会导致发育、电生理和行为缺陷。通过将毒素表达限制在较短的发育时期,可以区分这些缺陷。应用一种控制TNT时空表达的方法,我们发现,在蛹早期,它会损害视网膜的发育;在蛹中期,在突触形成期间,TNT会导致神经节层严重发育不全,这种情况会持续到成年期,使神经节层的光感受器-中间神经元突触失去功能。最后,在成年期,TNT既不阻断光感受器中的突触传递,也不会耗尽细胞中的n-Syb。我们的研究揭示了n-Syb在突触形成中一种新的、细胞类型特异性的功能,并且区分了两种突触类型:TNT抗性突触和TNT敏感性突触。如果将TNT用于神经回路分析,这些结果需要被考虑在内。

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