Max-Planck-Institute of Neurobiology, Martinsried, 82152, Germany.
Sci Rep. 2017 Oct 23;7(1):13823. doi: 10.1038/s41598-017-14076-7.
Optogenetic channels and ion pumps have become indispensable tools in neuroscience to manipulate neuronal activity and thus to establish synaptic connectivity and behavioral causality. Inhibitory channels are particularly advantageous to explore signal processing in neural circuits since they permit the functional removal of selected neurons on a trial-by-trial basis. However, applying these tools to study the visual system poses a considerable challenge because the illumination required for their activation usually also stimulates photoreceptors substantially, precluding the simultaneous probing of visual responses. Here, we explore the utility of the recently discovered anion channelrhodopsins GtACR1 and GtACR2 for application in the visual system of Drosophila. We first characterized their properties using a larval crawling assay. We further obtained whole-cell recordings from cells expressing GtACR1, which mediated strong and light-sensitive photocurrents. Finally, using physiological recordings and a behavioral readout, we demonstrate that GtACR1 enables the fast and reversible silencing of genetically targeted neurons within circuits engaged in visual processing.
光遗传学通道和离子泵已经成为神经科学中操纵神经元活动的不可或缺的工具,从而建立突触连接和行为因果关系。抑制性通道在探索神经回路中的信号处理方面特别有利,因为它们允许在逐个试验的基础上功能性地去除选定的神经元。然而,将这些工具应用于研究视觉系统带来了相当大的挑战,因为其激活所需的照明通常也会强烈刺激光感受器,从而排除了对视觉反应的同时探测。在这里,我们探索了最近发现的阴离子通道视紫红质 GtACR1 和 GtACR2 在果蝇视觉系统中的应用。我们首先使用幼虫爬行测定法对它们的特性进行了表征。我们进一步从表达 GtACR1 的细胞中获得了全细胞记录,该细胞介导了强烈且对光敏感的光电流。最后,使用生理记录和行为读数,我们证明 GtACR1 能够快速且可逆地沉默参与视觉处理的电路中基因靶向的神经元。