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首页> 外文期刊>Frontiers in Cellular Neuroscience >Ingenuity Pathway Analysis of Gene Expression Profiles in Distal Nerve Stump following Nerve Injury: Insights into Wallerian Degeneration
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Ingenuity Pathway Analysis of Gene Expression Profiles in Distal Nerve Stump following Nerve Injury: Insights into Wallerian Degeneration

机译:神经损伤后远端神经残端基因表达谱的独创性途径分析:对沃勒变性的认识

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Nerve injury is a common and difficult clinical problem worldwide with a high disability rate. Different from the central nervous system, the peripheral nervous system is able to regenerate after injury. Wallerian degeneration in the distal nerve stump contributes to the construction of a permissible microenvironment for peripheral nerve regeneration. To gain new molecular insights into Wallerian degeneration, this study aimed to identify differentially expressed genes and elucidate significantly involved pathways and cellular functions in the distal nerve stump following nerve injury. Microarray analysis showed that a few genes were differentially expressed at 0.5 and 1 h post nerve injury and later on a relatively larger number of genes were up-regulated or down-regulated. Ingenuity pathway analysis indicated that inflammation and immune response, cytokine signaling, cellular growth and movement, as well as tissue development and function were significantly activated following sciatic nerve injury. Notably, a cellular function highly related to nerve regeneration, which is called Nervous System Development and Function, was continuously activated from 4 days until 4 weeks post injury. Our results may provide further understanding of Wallerian degeneration from a genetic perspective, thus aiding the development of potential therapies for peripheral nerve injury.
机译:神经损伤是世界范围内普遍且棘手的临床问题,残疾率很高。与中枢神经系统不同,周围神经系统在受伤后能够再生。远端神经残端的Wallerian变性有助于周围神经再生的微环境的构建。为了获得有关Wallerian变性的新分子见解,本研究旨在鉴定差异表达的基因,并阐明神经损伤后远端神经残端中涉及的途径和细胞功能。基因芯片分析表明,一些基因在神经损伤后0.5和1 h差异表达,后来又有相对较多的基因被上调或下调。独创性途径分析表明,坐骨神经损伤后,炎症和免疫反应,细胞因子信号传导,细胞生长和运动以及组织发育和功能得到明显激活。值得注意的是,与神经再生高度相关的细胞功能(称为神经系统发育和功能)在受伤后4天至4周持续被激活。我们的结果可能会从遗传角度提供对Wallerian变性的进一步了解,从而有助于开发潜在的周围神经损伤疗法。

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