Son Jong-Hyun, Keefe Matthew D, Stevenson Tamara J, Barrios Joshua P, Anjewierden Scott, Newton James B, Douglass Adam D, Bonkowsky Joshua L
Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah.
Department of Neurobiology and Anatomy, University of Utah School of Medicine, Salt Lake City, Utah.
Sci Rep. 2016 Jan 5;6:18734. doi: 10.1038/srep18734.
Tools for genetically-determined visualization of synaptic circuits and interactions are necessary to build connectomics of the vertebrate brain and to screen synaptic properties in neurological disease models. Here we develop a transgenic FingR (fibronectin intrabodies generated by mRNA display) technology for monitoring synapses in live zebrafish. We demonstrate FingR labeling of defined excitatory and inhibitory synapses, and show FingR applicability for dissecting synapse dynamics in normal and disease states. Using our system we show that chronic hypoxia, associated with neurological defects in preterm birth, affects dopaminergic neuron synapse number depending on the developmental timing of hypoxia.
用于对突触回路和相互作用进行基因决定的可视化的工具,对于构建脊椎动物大脑的连接组学以及在神经疾病模型中筛选突触特性而言是必不可少的。在此,我们开发了一种转基因FingR(通过mRNA展示产生的纤连蛋白胞内抗体)技术,用于监测活斑马鱼中的突触。我们展示了FingR对特定兴奋性和抑制性突触的标记,并表明FingR适用于剖析正常和疾病状态下的突触动态。利用我们的系统,我们发现与早产时的神经缺陷相关的慢性缺氧,会根据缺氧的发育时间影响多巴胺能神经元突触的数量。