Department of Genetics and Evolution, University of Geneva, Geneva, Switzerland.
Methods Mol Biol. 2021;2130:207-219. doi: 10.1007/978-1-0716-0381-9_16.
Live imaging of the molecular clockwork within the circadian pacemaker neurons offers the unique possibility to study complex interactions between the molecular clock and neuronal communication within individual neurons and throughout the entire circadian circuitry. Here we describe how to establish brain explants and dissociated neuron culture from Drosophila larvae, guidelines for time-lapse fluorescence microscopy, and the method of image analysis. This approach enables the long-term monitoring of fluorescence signals of circadian reporters at single-cell resolution and can be also applicable to analyze real-time expression of other fluorescent probes in Drosophila neurons.
实时观察生物钟分子机制在生物钟神经元中的作用,为研究分子钟与单个神经元以及整个生物钟回路中的神经元通讯之间的复杂相互作用提供了独特的可能性。本文介绍了如何从小鼠胚胎中建立脑外植体和分离神经元培养物,以及用于延时荧光显微镜的指导原则和图像分析方法。该方法能够以单细胞分辨率长期监测生物钟报告基因的荧光信号,也可用于分析果蝇神经元中其他荧光探针的实时表达。