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首页> 外文期刊>The Journal of Comparative Neurology >Pax3 overexpression induces cell aggregation and perturbs commissural axon projection during embryonic spinal cord development
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Pax3 overexpression induces cell aggregation and perturbs commissural axon projection during embryonic spinal cord development

机译:PAX3过表达在胚胎脊髓开发期间引起电池聚集和Perturbs unmissupation Axon投影

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Pax3 is a transcription factor that belongs to the paired box family. In the developing spinal cord it is expressed in the dorsal commissural neurons, which project ascending axons contralaterally to form proper spinal cord-brain circuitry. While it has been shown that Pax3 induces cell aggregation in vitro, little is known about the role of Pax3 in cell aggregation and spinal circuit formation in vivo. We have reported that Pax3 is involved in neuron differentiation and that its overexpression induces ectopic cadherin-7 expression. In this study we report that Pax3 overexpression also induces cell aggregation in vivo. Tissue sections and open book preparations revealed that Pax3 overexpression prevents commissural axons from projecting to the contralateral side of the spinal cord. Cells overexpressing Pax3 aggregated in cell clusters that contained shortened neurites with perturbed axon growth and elongation. Pax3-specific shRNA partially rescued the morphological change induced by Pax3 overexpression in vivo. Our results indicate that the normal expression of Pax3 is necessary for proper axonal pathway finding and commissural axon projection. In conclusion, Pax3 regulates neural circuit formation during embryonic development. J. Comp. Neurol. 525:1618-1632, 2017. (c) 2016 Wiley Periodicals, Inc.
机译:PAX3是属于配对盒子家族的转录因子。在开发的脊髓中,它在背部外核神经元中表达,该神经元对逆向上升轴突以形成适当的脊髓脑电路。虽然已经表明pax3在体外诱导细胞聚集,但关于pax3在体内细胞聚集和椎间路形成中的作用很少。我们据报道,PAX3参与神经元分化,其过度表达诱导异位钙粘蛋白-7表达。在这项研究中,我们报告称PAX3过表达也诱导体内细胞聚集。组织切片和开放书准备表明,PAX3过表达可防止外壳轴突突出到脊髓的对侧。过表达PAX3的细胞在细胞簇中聚集,所述细胞簇含有较短的神经肌腱,具有扰动的轴突生长和伸长率。 PAX3特异性shRNA部分拯救了体内PAX3过表达诱导的形态变化。我们的结果表明,适当的轴突途径发现和连合轴突投影是必需PAX3的正常表达。总之,PAX3在胚胎发育过程中调节神经电路形成。 J. Comp。神经醇。 525:1618-1632,2017。(c)2016年Wiley期刊,Inc。

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