Department of Molecular and Systems Biology, Geisel School of Medicine, Dartmouth College, Hanover, NH, United States.
Department of Biological Sciences, Dartmouth College, Hanover, NH, United States.
Front Neural Circuits. 2020 May 8;14:22. doi: 10.3389/fncir.2020.00022. eCollection 2020.
Linking neural circuitry to behavior by mapping active neurons is a challenge. Both genetically encoded calcium indicators (GECIs) and intermediate early genes (IEGs) have been used to pinpoint active neurons during a stimulus or behavior but have drawbacks such as limiting the movement of the organism, requiring knowledge of the active region or having poor temporal resolution. Calcium-modulated photoactivatable ratiometric integrator (CaMPARI) was engineered to overcome these spatial-temporal challenges. CaMPARI is a photoconvertible protein that only converts from green to red fluorescence in the presence of high calcium concentration and 405 nm light. This allows the experimenter to precisely mark active neurons within defined temporal windows. The photoconversion can then be quantified by taking the ratio of the red fluorescence to the green. CaMPARI promises the ability to trace active neurons during a specific stimulus; however, CaMPARI's uses in adult have been limited to photoconversion during fly immobilization. Here, we demonstrate a method that allows photoconversion of multiple freely-moving intact adult flies during a stimulus. Flies were placed in a dish with filter paper wet with acetic acid (pH = 2) or neutralized acetic acid (pH = 7) and exposed to photoconvertible light (60 mW) for 30 min (500 ms on, 200 ms off). Immediately following photoconversion, whole flies were fixed and imaged by confocal microscopy. The red:green ratio was quantified for the DC4 glomerulus, a bundle of neurons expressing , an ionotropic receptor that senses acids in the antennal lobe. Flies exposed to acetic acid showed 1.3-fold greater photoconversion than flies exposed to neutralized acetic acid. This finding was recapitulated using a more physiological stimulus of apple cider vinegar. These results indicate that CaMPARI can be used to label neurons in intact, freely-moving adult flies and will be useful for identifying the circuitry underlying complex behaviors.
通过绘制活跃神经元来将神经回路与行为联系起来是一个挑战。遗传编码钙指示剂(GECIs)和早期基因(IEGs)都被用于在刺激或行为期间精确定位活跃神经元,但存在限制生物体运动、需要了解活跃区域或时间分辨率差等缺点。钙调制光激活比率积分器(CaMPARI)被设计用来克服这些时空挑战。CaMPARI 是一种光可转换蛋白,只有在高钙浓度和 405nm 光存在下才会从绿色转换为红色荧光。这使得实验者能够在定义的时间窗口内精确标记活跃神经元。通过测量红色荧光与绿色荧光的比值可以对光转换进行定量。CaMPARI 有望在特定刺激期间追踪活跃神经元;然而,CaMPARI 在成年中的应用仅限于在果蝇固定时进行光转换。在这里,我们展示了一种允许在刺激期间对多个自由移动的完整成年果蝇进行光转换的方法。将果蝇放置在盛有浸有乙酸(pH=2)或中和乙酸(pH=7)的滤纸的培养皿中,并暴露于可光转换的光(60mW)下 30 分钟(500ms 开启,200ms 关闭)。光转换后,立即通过共聚焦显微镜固定和成像整个果蝇。量化 DC4 神经节的红:绿比值,这是一束表达 的神经元, 是一种离子型受体,可感知触角叶中的酸。与中性化乙酸相比,暴露于乙酸中的果蝇的光转换增加了 1.3 倍。使用更生理的苹果醋刺激重复了这一发现。这些结果表明,CaMPARI 可用于标记完整、自由移动的成年果蝇中的神经元,对于确定复杂行为的神经回路将非常有用。