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B-RAF kinase drives developmental axon growth and promotes axon regeneration in the injured mature CNS.B-RAF 激酶驱动发育性轴突生长,并促进成熟中枢神经系统损伤后的轴突再生。
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A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing.一套基于 Cre 的依赖光遗传学的转基因小鼠工具,用于光诱导的激活和沉默。
Nat Neurosci. 2012 Mar 25;15(5):793-802. doi: 10.1038/nn.3078.
3
DiI-labeling of DRG neurons to study axonal branching in a whole mount preparation of mouse embryonic spinal cord.用DiI标记背根神经节神经元,以研究小鼠胚胎脊髓整装标本中的轴突分支。
J Vis Exp. 2011 Dec 13(58):3667. doi: 10.3791/3667.
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Small fibers in Fabry disease: baseline and follow-up data under enzyme replacement therapy.法布里病的小纤维:酶替代治疗的基线和随访数据。
J Peripher Nerv Syst. 2011 Dec;16(4):304-14. doi: 10.1111/j.1529-8027.2011.00365.x.
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Raf kinase signaling functions in sensory neuron differentiation and axon growth in vivo.Raf激酶信号传导在体内感觉神经元分化和轴突生长中发挥作用。
Nat Neurosci. 2007 May;10(5):598-607. doi: 10.1038/nn1898. Epub 2007 Mar 29.
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Cutaneous sensory abnormalities in children and adolescents with complex regional pain syndromes.患有复杂性区域疼痛综合征的儿童和青少年的皮肤感觉异常
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Expression of endogenous oncogenic V600EB-raf induces proliferation and developmental defects in mice and transformation of primary fibroblasts.内源性致癌性V600E B-raf的表达诱导小鼠增殖和发育缺陷以及原代成纤维细胞的转化。
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8
A neurotrophin signaling cascade coordinates sympathetic neuron development through differential control of TrkA trafficking and retrograde signaling.神经营养因子信号级联通过对TrkA运输和逆行信号的差异控制来协调交感神经元的发育。
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Going the distance, or not, with neurotrophin signals.神经营养因子信号传导的远近问题
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10
Expressing TrkC from the TrkA locus causes a subset of dorsal root ganglia neurons to switch fate.从TrkA基因座表达TrkC会导致一部分背根神经节神经元转变命运。
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小鼠胚胎感觉轴突投射的整体成像。

Whole-mount imaging of mouse embryo sensory axon projections.

作者信息

O'Donovan Kevin J, O'Keeffe Catherine, Zhong Jian

机构信息

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;

出版信息

J Vis Exp. 2014 Dec 9(94):52212. doi: 10.3791/52212.

DOI:10.3791/52212
PMID:25549235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4299441/
Abstract

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.

摘要

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。