Department of Neurological Sciences, Multiple Sclerosis Center, Rush University Medical Center, 1725 W. Harrison Street, Suite 309, Chicago, IL 60612, USA.
J Neuroimmune Pharmacol. 2010 Jun;5(2):260-5. doi: 10.1007/s11481-010-9193-z. Epub 2010 Feb 23.
Interferon regulatory factor 1 (IRF-1) is a transcription factor that has been implicated in the disease mechanisms of experimental autoimmune encephalomyelitis (EAE). In this study, we examined the role of central nervous system (CNS) expression of IRF-1 in the natural course of EAE. In an effort to dissect the CNS effects from the peripheral immune effects of IRF-1, we generated bone marrow chimera mice that differentially expressed IRF-1 in the CNS and in the immune system. We found that mice lacking IRF-1 in the CNS developed significantly milder clinical symptoms and shorter disease duration compared to those with wild-type background. Based on these results, we concluded that the CNS expression of IRF-1 regulates the disease process in EAE. Our findings are relevant to the inflammatory mechanisms involved in multiple sclerosis and may provide a basis for development of novel therapeutic targets of the disease.
干扰素调节因子 1(IRF-1)是一种转录因子,它与实验性自身免疫性脑脊髓炎(EAE)的疾病机制有关。在这项研究中,我们研究了中枢神经系统(CNS)中 IRF-1 的表达在 EAE 的自然病程中的作用。为了从 IRF-1 的外周免疫作用中分离出 CNS 效应,我们生成了骨髓嵌合体小鼠,它们在 CNS 和免疫系统中差异表达 IRF-1。我们发现,与野生型背景相比,缺乏 CNS 中 IRF-1 的小鼠表现出明显较轻的临床症状和较短的疾病持续时间。基于这些结果,我们得出结论,CNS 中 IRF-1 的表达调节 EAE 中的疾病过程。我们的发现与多发性硬化症中涉及的炎症机制有关,并可能为该疾病的新型治疗靶点的开发提供基础。