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病毒转导神经示踪技术的进展。

Advances in viral transneuronal tracing.

机构信息

Laboratoire de Neurobiologie Cellulaire et Moléculaire (NBCM) UPR9040, Gif sur Yvette, France.

出版信息

J Neurosci Methods. 2010 Dec 15;194(1):2-20. doi: 10.1016/j.jneumeth.2009.12.001. Epub 2010 Jan 6.

Abstract

Powerful transneuronal tracing technologies exploit the ability of some neurotropic viruses to travel across neuronal pathways and to function as self-amplifying markers. Two main classes of viral transneuronal tracers are available, derived from alpha-herpesviruses (Herpes Simplex virus type 1, Pseudorabies) and rabies virus. Depending on the virus type and strain, there are major differences with regard to host range, peripheral uptake, replication mechanisms, transport direction and specificity. While alpha-herpesviruses are the tracers of choice for studying autonomic innervation, rabies virus is the ideal tool for studying motor innervation, since its peripheral uptake occurs exclusively at motor endplates. Rabies virus is the only viral tracer that is entirely specific, as it moves exclusively across chemical synapses by strictly unidirectional (retrograde) transneuronal transfer without altering neuronal metabolism, allowing for the stepwise, time-dependent, identification of neuronal networks across an unlimited number of synapses. This review will highlight and contrast the different properties of these viral tracers, and summarize the methodological issues that are critical for the appropriate execution and interpretation of transneuronal tracing studies. Combinations of viral tracing with other methodologies will be evaluated. Emerging technologies, based on genetically modified herpes and rabies tracers, will be also discussed and put in perspective.

摘要

强大的跨神经元示踪技术利用了一些神经营养病毒穿越神经元通路的能力,并将其作为自我放大的标记物。有两种主要的病毒跨神经元示踪剂,分别来自α-疱疹病毒(单纯疱疹病毒 1 型、伪狂犬病病毒)和狂犬病病毒。根据病毒类型和株的不同,在宿主范围、外周摄取、复制机制、运输方向和特异性方面存在显著差异。虽然α-疱疹病毒是研究自主神经支配的首选示踪剂,但狂犬病病毒是研究运动神经支配的理想工具,因为其外周摄取仅发生在运动终板。狂犬病病毒是唯一完全特异的病毒示踪剂,因为它仅通过严格的单向(逆行)跨神经元传递穿过化学突触,而不改变神经元代谢,从而允许在不改变神经元代谢的情况下,逐步、时间依赖地识别跨越无数个突触的神经元网络。这篇综述将重点介绍和对比这些病毒示踪剂的不同特性,并总结对于跨神经元示踪研究的正确执行和解释至关重要的方法学问题。还将评估病毒示踪与其他方法学的结合。此外,还将讨论和展望基于遗传修饰的疱疹和狂犬病示踪剂的新兴技术。

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