Howard Hughes Medical Institute, Janelia Farm Research Campus, 19700 Helix Drive, Ashburn, VA 20147, USA.
Department of Zoology, University of Cambridge, Downing St, Cambridge, CB2 3EJ, UK.
Sci Rep. 2017 Jan 13;7:40433. doi: 10.1038/srep40433.
The delivery of tracers into populations of neurons is essential to visualize their anatomy and analyze their function. In some model systems genetically-targeted expression of fluorescent proteins is the method of choice; however, these genetic tools are not available for most organisms and alternative labeling methods are very limited. Here we describe a new method for neuronal labelling by electrophoretic dye delivery from a suction electrode directly through the neuronal sheath of nerves and ganglia in insects. Polar tracer molecules were delivered into the locust auditory nerve without destroying its function, simultaneously staining peripheral sensory structures and central axonal projections. Local neuron populations could be labelled directly through the surface of the brain, and in-vivo optical imaging of sound-evoked activity was achieved through the electrophoretic delivery of calcium indicators. The method provides a new tool for studying how stimuli are processed in peripheral and central sensory pathways and is a significant advance for the study of nervous systems in non-model organisms.
将示踪剂递送到神经元群体中对于可视化它们的解剖结构和分析它们的功能至关重要。在某些模型系统中,基因靶向表达荧光蛋白是首选方法;然而,这些遗传工具并不适用于大多数生物体,并且替代标记方法非常有限。在这里,我们描述了一种新的方法,通过从抽吸电极电泳递送来标记神经元,直接穿过昆虫的神经和神经节的神经元鞘。极性示踪分子被递送到蝗虫听觉神经中,而不会破坏其功能,同时对周围感觉结构和中枢轴突投射进行染色。可以通过大脑表面直接标记局部神经元群体,并通过电泳递送来钙指示剂实现对声音诱发活动的活体光学成像。该方法为研究刺激在周围和中枢感觉通路中的处理方式提供了新工具,并且是研究非模式生物神经系统的重要进展。