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比较不同发育阶段小鼠周围传出和传入神经纤维的转录组特征。

Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice.

机构信息

Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, JS, 226001, China.

The Hand Surgery Research Center, Department of Hand Surgery, Affiliated Hospital of Nantong University, Nantong, JS, 226001, China.

出版信息

Sci Rep. 2018 Aug 10;8(1):11990. doi: 10.1038/s41598-018-30463-0.

Abstract

Peripheral nerve injury impairs motor and sensory function in humans, and its functional recovery largely depends on the axonal outgrowth required for the accurate reinnervation of appropriate targets. To better understand how motor and sensory nerve fibres select their terminal pathways, an unbiased cDNA microarray analysis was conducted to examine differential gene expression patterns in peripheral efferent and afferent fibres at different developmental stages in mice. Gene ontology (GO) and Kyoto Enrichment of Genes and Genomes (KEGG) analyses revealed common and distinct features of enrichment for differentially expressed genes during motor and sensory nerve fibre development. Ingenuity Pathway Analysis (IPA) further indicated that the key differentially expressed genes were associated with trans-synaptic neurexin-neuroligin signalling components and a variety of gamma-aminobutyric acid (GABA) receptors. The aim of this study was to generate a framework of gene networks regulated during motor and sensory neuron differentiation/maturation. These data may provide new clues regarding the underlying cellular and molecular mechanisms that determine the intrinsic capacity of neurons to regenerate after peripheral nerve injury. Our findings may thus facilitate further development of a potential intervention to manipulate the therapeutic efficiency of peripheral nerve repair in the clinic.

摘要

周围神经损伤会损害人类的运动和感觉功能,其功能的恢复在很大程度上取决于轴突的生长,这是神经准确再支配合适靶组织所必需的。为了更好地理解运动和感觉神经纤维如何选择其终末途径,我们对不同发育阶段小鼠的周围传出和传入纤维进行了无偏 cDNA 微阵列分析,以检测差异基因表达模式。基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析揭示了运动和感觉神经纤维发育过程中差异表达基因的常见和独特的富集特征。IPA 进一步表明,关键差异表达基因与跨突触神经连接蛋白-神经黏附素信号转导组件和多种γ-氨基丁酸(GABA)受体有关。本研究旨在构建一个受运动和感觉神经元分化/成熟调控的基因网络框架。这些数据可能为确定神经元在周围神经损伤后内在再生能力的潜在细胞和分子机制提供新的线索。因此,我们的发现可能有助于进一步开发一种潜在的干预措施,以提高临床外周神经修复的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ba9/6086926/b803da64a845/41598_2018_30463_Fig1_HTML.jpg

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