Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
Nat Protoc. 2012 Jul 12;7(8):1470-8. doi: 10.1038/nprot.2012.079.
Optogenetics is a powerful tool that enables the spatiotemporal control of neuronal activity and circuits in behaving animals. Here, we describe our protocol for optical activation of neurons in Drosophila larvae. As an example, we discuss the use of optogenetics to activate larval nociceptors and nociception behaviors in the third-larval instar. We have previously shown that, using spatially defined GAL4 drivers and potent UAS (upstream activation sequence)-channelrhodopsin-2∷YFP transgenic strains developed in our laboratory, it is possible to manipulate neuronal populations in response to illumination by blue light and to test whether the activation of defined neural circuits is sufficient to shape behaviors of interest. Although we have only used the protocol described here in larval stages, the procedure can be adapted to study neurons in adult flies--with the caveat that blue light may not sufficiently penetrate the adult cuticle to stimulate neurons deep in the brain. This procedure takes 1 week to culture optogenetic flies and ~1 h per group for the behavioral assays.
光遗传学是一种强大的工具,可实现行为动物中神经元活动和回路的时空控制。在这里,我们描述了在果蝇幼虫中用光激活神经元的方案。作为一个例子,我们讨论了用光遗传学来激活幼虫伤害感受器和第三龄幼虫的伤害感受行为。我们之前已经表明,使用空间定义的 GAL4 驱动和我们实验室中开发的强大 UAS(上游激活序列)-通道视紫红质-2∷YFP 转基因品系,可以响应蓝光照射来操纵神经元群体,并测试激活特定的神经回路是否足以塑造感兴趣的行为。尽管我们仅在幼虫阶段使用了此处描述的方案,但该程序可以适应研究成年果蝇中的神经元——但要注意,蓝光可能不足以穿透成年的外骨骼来刺激大脑深处的神经元。该程序需要 1 周时间来培养光遗传学果蝇,每组行为测定需要 1 小时。