首页> 美国卫生研究院文献>Frontiers in Neurology >Targeting the Full Length of the Motor End Plate Regions in the Mouse Forelimb Increases the Uptake of Fluoro-Gold into Corresponding Spinal Cord Motor Neurons
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Targeting the Full Length of the Motor End Plate Regions in the Mouse Forelimb Increases the Uptake of Fluoro-Gold into Corresponding Spinal Cord Motor Neurons

机译:靶向小鼠前肢中运动端板区域的全长会增加相应的脊髓运动神经元对氟金的吸收。

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摘要

Lower motor neuron dysfunction is one of the most debilitating motor conditions. In this regard, transgenic mouse models of various lower motor neuron dysfunctions provide insight into the mechanisms underlying these pathologies and can also aid the development of new therapies. Viral-mediated gene therapy can take advantage of the muscle-motor neuron topographical relationship to shuttle therapeutic genes into specific populations of motor neurons in these mouse models. In this context, motor end plates (MEPs) are highly specialized regions on the skeletal musculature that offer direct access to the pre-synaptic nerve terminals, henceforth to the spinal cord motor neurons. The aim of this study was two-folded. First, it was to characterize the exact position of the MEP regions for several muscles of the mouse forelimb using acetylcholinesterase histochemistry. This MEP-muscle map was then used to guide a series of intramuscular injections of Fluoro-Gold (FG) in order to characterize the distribution of the innervating motor neurons. This analysis revealed that the MEPs are typically organized in an orthogonal fashion across the muscle fibers and extends throughout the full width of each muscle. Furthermore, targeting the full length of the MEP regions gave rise labeled motor neurons that are organized into columns spanning through more spinal cord segments than previously reported. The present analysis suggests that targeting the full width of the muscles’ MEP regions with FG increases the somatic availability of the tracer. This process ensures a greater uptake of the tracer by the pre-synaptic nerve terminals, hence maximizing the labeling in spinal cord motor neurons. This investigation should have positive implications for future studies involving the somatic delivery of therapeutic genes into motor neurons for the treatment of various motor dysfunctions.
机译:下运动神经元功能障碍是最使人衰弱的运动状况之一。在这方面,各种下运动神经元功能障碍的转基因小鼠模型可以洞悉这些病理的潜在机制,也可以帮助开发新疗法。在这些小鼠模型中,病毒介导的基因治疗可以利用肌肉-运动神经元的地形关系将治疗基因穿梭到特定的运动神经元群体中。在这种情况下,运动终板(MEP)是骨骼肌组织上高度专门化的区域,可直接进入突触前神经末梢,此后便到达脊髓运动神经元。这项研究的目的有两个方面。首先,它是使用乙酰胆碱酯酶组织化学方法表征小鼠前肢几条肌肉的MEP区域的确切位置。然后使用该MEP肌肉图来指导一系列氟金(FG)的肌内注射,以表征神经支配的运动神经元的分布。该分析表明,MEP通常在肌肉纤维上以正交的方式组织,并延伸到每条肌肉的整个宽度。此外,针对MEP区域的全长,产生了标记的运动神经元,这些神经元被组织成比以前报道的更多的脊髓节段。目前的分析表明,使用FG瞄准肌肉MEP区域的整个宽度会增加示踪剂的体细胞利用率。此过程可确保突触前神经末梢对示踪剂的摄取更大,从而使脊髓运动神经元的标记最大化。这项研究对涉及将治疗性基因向运动神经元的躯体传递以治疗各种运动功能障碍的未来研究具有积极意义。

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