Department of Cellular and Molecular Physiology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.
Cell. 2013 Aug 15;154(4):904-13. doi: 10.1016/j.cell.2013.07.027. Epub 2013 Aug 8.
Nervous systems process information by integrating the electrical activity of neurons in complex networks. This motivates the long-standing interest in using optical methods to simultaneously monitor the membrane potential of multiple genetically targeted neurons via expression of genetically encoded fluorescent voltage indicators (GEVIs) in intact neural circuits. No currently available GEVIs have demonstrated robust signals in intact brain tissue that enable reliable recording of individual electrical events simultaneously in multiple neurons. Here, we show that the recently developed "ArcLight" GEVI robustly reports both subthreshold events and action potentials in genetically targeted neurons in the intact Drosophila fruit fly brain and reveals electrical signals in neurite branches. In the same way that genetically encoded fluorescent sensors have revolutionized the study of intracellular Ca(2+) signals, ArcLight now enables optical measurement in intact neural circuits of membrane potential, the key cellular parameter that underlies neuronal information processing.
神经系统通过整合神经元在复杂网络中的电活动来处理信息。这激发了人们长期以来的兴趣,即使用光学方法通过在完整的神经回路中表达遗传编码的荧光电压指示剂 (GEVI) 来同时监测多个基因靶向神经元的膜电位。目前尚无可用的 GEVIs 能够在完整的脑组织中产生稳健的信号,从而能够可靠地同时在多个神经元中记录单个电事件。在这里,我们表明,最近开发的“ArcLight”GEVI 能够在完整的果蝇大脑中基因靶向神经元中稳健地报告亚阈事件和动作电位,并揭示神经突分支中的电信号。就像遗传编码的荧光传感器彻底改变了细胞内 Ca(2+)信号的研究一样,ArcLight 现在使膜电位的完整神经回路中的光学测量成为可能,膜电位是构成神经元信息处理的关键细胞参数。