Zeis T, Kinter J, Herrero-Herranz E, Weissert R, Schaeren-Wiemers N
Neurobiology, Department of Biomedicine and Neurology, University Hospital Basel, Pharmacenter, Klingelbergstrasse 50-70, 4056 Basel, Switzerland.
J Neuroimmunol. 2008 Dec 15;205(1-2):10-9. doi: 10.1016/j.jneuroim.2008.09.009. Epub 2008 Oct 23.
Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS). Recent studies suggest that, beside focal lesions, diffuse inflammatory and degenerative processes take place throughout the MS brain. Especially, molecular alterations in the so-called normal appearing white matter suggest the induction of neuroprotective mechanisms against oxidative stress preserving cellular homeostasis and function. In this study we investigated whether in an animal model for MS, namely in experimental autoimmune encephalomyelitis (EAE), similar changes occur. We isolated normal appearing white and grey matter from the corpus callosum and the above lying cerebral cortex from DA rats with rMOG-induced EAE and carried out a gene expression analysis. Examination of corpus callosum revealed only minor changes in EAE rats. In contrast, we identified a number of gene expression alterations in the cerebral cortex even though morphological and cellular alterations were not evident. One of the most striking observations was the downregulation of genes involved in mitochondrial function as well as a whole set of genes coding for different glutamate receptors. Our data imply that molecular alterations are present in neurons far distant to inflammatory demyelinating lesions. These alterations might reflect degenerative processes induced by lesion-mediated axonal injury in the spinal cord. Our results indicate that the MOG-induced EAE in DA rats is a valuable model to analyze neuronal alterations due to axonal impairment in an acute phase of a MS-like disease, and could be used for development of neuroprotective strategies.
多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性炎性脱髓鞘疾病。最近的研究表明,除了局灶性病变外,MS脑内还会发生弥漫性炎症和退行性病变。特别是,所谓正常外观白质中的分子改变提示诱导了针对氧化应激的神经保护机制,以维持细胞内稳态和功能。在本研究中,我们调查了在MS动物模型,即实验性自身免疫性脑脊髓炎(EAE)中是否会发生类似变化。我们从患有重组髓鞘少突胶质细胞糖蛋白(rMOG)诱导的EAE的DA大鼠的胼胝体和上方的大脑皮质中分离出外观正常的白质和灰质,并进行了基因表达分析。对胼胝体的检查显示EAE大鼠中只有轻微变化。相比之下,尽管形态学和细胞改变不明显,但我们在大脑皮质中鉴定出了一些基因表达改变。最显著的发现之一是参与线粒体功能的基因以及一组编码不同谷氨酸受体的基因下调。我们的数据表明,在远离炎性脱髓鞘病变的神经元中存在分子改变。这些改变可能反映了脊髓中病变介导的轴突损伤所诱导的退行性过程。我们的结果表明,DA大鼠中MOG诱导的EAE是一个有价值的模型,可用于分析MS样疾病急性期轴突损伤引起的神经元改变,并可用于开发神经保护策略。