Suppr超能文献

自身免疫性视神经炎中的神经退行性变与神经元中淀粉样前体蛋白(APP)切割改变及p53上调有关。

Neurodegeneration in Autoimmune Optic Neuritis Is Associated with Altered APP Cleavage in Neurons and Up-Regulation of p53.

作者信息

Herold Sabine, Kumar Prateek, Wichert Sven P, Kretzschmar Benedikt, Bähr Mathias, Rossner Moritz J, Hein Katharina

机构信息

Department of Neurology, University Medicine Göttingen, Göttingen, Germany.

Molecular and Behavioral Neurobiology, Department of Psychiatry, Ludwig Maximilians University Munich, Munich, Germany.

出版信息

PLoS One. 2015 Oct 1;10(10):e0138852. doi: 10.1371/journal.pone.0138852. eCollection 2015.

Abstract

Multiple Sclerosis (MS) is a chronic autoimmune inflammatory disease of the central nervous system (CNS). Histopathological and radiological analysis revealed that neurodegeneration occurs early in the disease course. However, the pathological mechanisms involved in neurodegeneration are poorly understood. Myelin oligodendrocyte glycoprotein (MOG)-induced experimental autoimmune encephalomyelitis (EAE) in Brown Norway rats (BN-rats) is a well-established animal model, especially of the neurodegenerative aspects of MS. Previous studies in this animal model indicated that loss of retinal ganglion cells (RGCs), the neurons that form the axons of the optic nerve, occurs in the preclinical phase of the disease and is in part independent of overt histopathological changes of the optic nerve. Therefore, the aim of this study was to identify genes which are involved in neuronal cell loss at different disease stages of EAE. Furthermore, genes that are highly specific for autoimmune-driven neurodegeneration were compared to those regulated in RGCs after optic nerve axotomy at corresponding time points. Using laser capture micro dissection we isolated RNA from unfixed RGCs and performed global transcriptome analysis of retinal neurons. In total, we detected 582 genes sequentially expressed in the preclinical phase and 1150 genes in the clinical manifest EAE (P < 0.05, fold-induction >1.5). Furthermore, using ingenuity pathway analysis (IPA), we identified amyloid precursor protein (APP) as a potential upstream regulator of changes in gene expression in the preclinical EAE but neither in clinical EAE, nor at any time point after optic nerve transection. Therefore, the gene pathway analysis lead to the hypothesis that altered cleavage of APP in neurons in the preclinical phase of EAE leads to the enhanced production of APP intracellular domain (AICD), which in turn acts as a transcriptional regulator and thereby initiates an apoptotic signaling cascade via up-regulation of the target gene p53.

摘要

多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性自身免疫性炎症性疾病。组织病理学和放射学分析表明,神经退行性变在疾病进程早期就已发生。然而,神经退行性变所涉及的病理机制仍知之甚少。髓鞘少突胶质细胞糖蛋白(MOG)诱导的棕色挪威大鼠(BN大鼠)实验性自身免疫性脑脊髓炎(EAE)是一种成熟的动物模型,尤其是针对MS神经退行性变方面。此前在该动物模型中的研究表明,视网膜神经节细胞(RGCs)的丢失,即构成视神经轴突的神经元,发生在疾病的临床前期,且部分独立于视神经明显的组织病理学变化。因此,本研究的目的是确定在EAE不同疾病阶段参与神经元细胞丢失的基因。此外,将自身免疫驱动的神经退行性变高度特异的基因与相应时间点视神经切断后RGCs中受调控的基因进行比较。我们使用激光捕获显微切割技术从未固定的RGCs中分离RNA,并对视网膜神经元进行全转录组分析。总共,我们检测到在临床前期依次表达的582个基因以及临床显性EAE中的1150个基因(P < 0.05,诱导倍数>1.5)。此外,使用 Ingenuity 通路分析(IPA),我们确定淀粉样前体蛋白(APP)是临床前期EAE基因表达变化的潜在上游调节因子,但在临床EAE中以及视神经横断后的任何时间点均不是。因此,基因通路分析得出一个假设:EAE临床前期神经元中APP的切割改变导致APP细胞内结构域(AICD)产生增加,AICD进而作为转录调节因子,通过上调靶基因p53启动凋亡信号级联反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b19e/4591258/aa71f9975d9a/pone.0138852.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验