O'Donovan Kevin J, O'Keeffe Catherine, Zhong Jian
Brain and Mind Research Institute, Burke Medical Research Institute, Weill Medical College of Cornell University.
Brain and Mind Research Institute, Burke Medical Research Institute, Weill Medical College of Cornell University;
J Vis Exp. 2014 Dec 9(94):52212. doi: 10.3791/52212.
The visualization of full-length neuronal projections in embryos is essential to gain an understanding of how mammalian neuronal networks develop. Here we describe a method to label in situ a subset of dorsal root ganglion (DRG) axon projections to assess their phenotypic characteristics using several genetically manipulated mouse lines. The TrkA-positive neurons are nociceptor neurons, dedicated to the transmission of pain signals. We utilize a TrkA(taulacZ) mouse line to label the trajectories of all TrkA-positive peripheral axons in the intact mouse embryo. We further breed the TrkA(taulacZ) line onto a Bax null background, which essentially abolishes neuronal apoptosis, in order to assess growth-related questions independently of possible effects of genetic manipulations on neuronal survival. Subsequently, genetically modified mice of interest are bred with the TrkA(taulacZ)/Bax null line and are then ready for study using the techniques described herein. This presentation includes detailed information on mouse breeding plans, genotyping at the time of dissection, tissue preparation, staining and clearing to allow for visualization of full-length axonal trajectories in whole-mount preparation.
在胚胎中可视化全长神经元投射对于理解哺乳动物神经元网络如何发育至关重要。在这里,我们描述了一种原位标记背根神经节(DRG)轴突投射子集的方法,以使用几种基因操作的小鼠品系评估其表型特征。TrkA阳性神经元是伤害感受器神经元,专门负责疼痛信号的传递。我们利用TrkA(tauLacZ)小鼠品系来标记完整小鼠胚胎中所有TrkA阳性外周轴突的轨迹。我们进一步将TrkA(tauLacZ)品系培育到Bax基因敲除的背景上,这基本上消除了神经元凋亡,以便独立于基因操作对神经元存活的可能影响来评估与生长相关的问题。随后,将感兴趣的基因修饰小鼠与TrkA(tauLacZ)/Bax基因敲除品系进行杂交,然后就可以使用本文所述的技术进行研究。本报告包括有关小鼠繁殖计划、解剖时的基因分型、组织制备、染色和透明处理的详细信息,以便在整装标本中可视化全长轴突轨迹。