Ciabatti Ernesto, González-Rueda Ana, Mariotti Letizia, Morgese Fabio, Tripodi Marco
Division of Neurobiology, MRC Laboratory of Molecular Biology, Cambridge, UK.
Division of Neurobiology, MRC Laboratory of Molecular Biology, Cambridge, UK.
Cell. 2017 Jul 13;170(2):382-392.e14. doi: 10.1016/j.cell.2017.06.014. Epub 2017 Jul 6.
Neural networks are emerging as the fundamental computational unit of the brain and it is becoming progressively clearer that network dysfunction is at the core of a number of psychiatric and neurodegenerative disorders. Yet, our ability to target specific networks for functional or genetic manipulations remains limited. Monosynaptically restricted rabies virus facilitates the anatomical investigation of neural circuits. However, the inherent cytotoxicity of the rabies largely prevents its implementation in long-term functional studies and the genetic manipulation of neural networks. To overcome this limitation, we developed a self-inactivating ΔG-rabies virus (SiR) that transcriptionally disappears from the infected neurons while leaving permanent genetic access to the traced network. SiR provides a virtually unlimited temporal window for the study of network dynamics and for the genetic and functional manipulation of neural circuits in vivo without adverse effects on neuronal physiology and circuit function.
神经网络正逐渐成为大脑的基本计算单元,并且越来越清楚的是,网络功能障碍是许多精神疾病和神经退行性疾病的核心。然而,我们针对特定网络进行功能或基因操作的能力仍然有限。单突触限制的狂犬病病毒有助于神经回路的解剖学研究。然而,狂犬病病毒固有的细胞毒性在很大程度上阻碍了其在长期功能研究和神经网络基因操作中的应用。为了克服这一限制,我们开发了一种自失活的ΔG-狂犬病病毒(SiR),它在感染的神经元中转录消失,同时为被追踪的网络留下永久的基因访问途径。SiR为体内网络动力学研究以及神经回路的基因和功能操作提供了几乎无限的时间窗口,而不会对神经元生理学和回路功能产生不利影响。