Department of Genetics and Dominick Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 1041, USA.
Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University, New York, NY 10027, USA.
Genetics. 2021 Aug 9;218(4). doi: 10.1093/genetics/iyab072.
The model research animal Caenorhabditis elegans has unique properties making it particularly advantageous for studies of the nervous system. The nervous system is composed of a stereotyped complement of neurons connected in a consistent manner. Here, we describe methods for studying nervous system structure and function. The transparency of the animal makes it possible to visualize and identify neurons in living animals with fluorescent probes. These methods have been recently enhanced for the efficient use of neuron-specific reporter genes. Because of its simple structure, for a number of years, C. elegans has been at the forefront of connectomic studies defining synaptic connectivity by electron microscopy. This field is burgeoning with new, more powerful techniques, and recommended up-to-date methods are here described that encourage the possibility of new work in C. elegans. Fluorescent probes for single synapses and synaptic connections have allowed verification of the EM reconstructions and for experimental approaches to synapse formation. Advances in microscopy and in fluorescent reporters sensitive to Ca2+ levels have opened the way to observing activity within single neurons across the entire nervous system.
秀丽隐杆线虫这种模式生物具有独特的属性,使其特别有利于神经系统的研究。神经系统由以一致方式连接的定型神经元组成。在这里,我们描述了研究神经系统结构和功能的方法。该动物的透明性使其能够使用荧光探针在活体动物中可视化和识别神经元。最近,这些方法得到了改进,以便更有效地利用神经元特异性报告基因。由于其结构简单,多年来,秀丽隐杆线虫一直处于连接组学研究的前沿,通过电子显微镜定义突触连接。这个领域正在涌现出许多新的、更强大的技术,这里描述了推荐的最新方法,鼓励在秀丽隐杆线虫中开展新的工作。用于单个突触和突触连接的荧光探针允许对 EM 重建进行验证,并进行实验方法以研究突触形成。显微镜技术和对 Ca2+ 水平敏感的荧光报告基因的进步为观察整个神经系统中单神经元的活动开辟了道路。