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白细胞介素7受体(IL-7R)的下调促成中枢神经系统脱髓鞘。

Down-regulation of interleukin 7 receptor (IL-7R) contributes to central nervous system demyelination.

作者信息

Lei Xudan, Cai Shijiao, Chen Yang, Cui Jianlin, Wang Yajie, Li Zongjin, Li Yuhao

机构信息

Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin 300071, China.

出版信息

Oncotarget. 2017 Apr 25;8(17):28395-28407. doi: 10.18632/oncotarget.16081.

Abstract

Interleukin 7 receptor (IL-7R) has been associated with the pathogenesis of multiple sclerosis (MS), though the mechanisms are not clear. Because myelin expression is highly conserved between zebrafish and mammals, zebrafish have become an ideal model for studying demyelination. We used a transgenic (Tg; mbp:nfsB-egfp) zebrafish line in which oligodendrocytes expressed green fluorescent protein (GFP) from the larval stage to adulthood. Exposing adult transgenic zebrafish to metronidazole induced demyelination that resembled the morphological changes associated with the early stages of MS. The metronidazole-induced demyelination was confirmed by magnetic resonance imaging (MRI) for the first time. Microarray analysis revealed down-regulation of IL-7R during demyelination. Targeted knockdown of IL-7R demonstrated that IL-7R is essential for myelination in embryonic and larval zebrafish. Moreover, IL-7R down-regulation induced signaling via the JAK/STAT pathway leading to apoptosis in oligodendrocytes. These findings contribute to our understanding of the role of IL-7R in demyelination, and provide a rationale for the development of IL-7R-based therapies for MS and other demyelinating diseases.

摘要

白细胞介素7受体(IL-7R)与多发性硬化症(MS)的发病机制有关,但其机制尚不清楚。由于斑马鱼和哺乳动物之间的髓鞘表达高度保守,斑马鱼已成为研究脱髓鞘的理想模型。我们使用了一种转基因(Tg;mbp:nfsB-egfp)斑马鱼品系,其中少突胶质细胞从幼虫阶段到成年阶段都表达绿色荧光蛋白(GFP)。将成年转基因斑马鱼暴露于甲硝唑会诱导脱髓鞘,这与MS早期相关的形态学变化相似。首次通过磁共振成像(MRI)证实了甲硝唑诱导的脱髓鞘。微阵列分析显示脱髓鞘过程中IL-7R表达下调。靶向敲低IL-7R表明IL-7R对胚胎和幼虫斑马鱼的髓鞘形成至关重要。此外,IL-7R下调通过JAK/STAT途径诱导信号传导,导致少突胶质细胞凋亡。这些发现有助于我们理解IL-7R在脱髓鞘中的作用,并为开发基于IL-7R的MS和其他脱髓鞘疾病治疗方法提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7064/5438658/86ed5a174bf2/oncotarget-08-28395-g001.jpg

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