Voskuhl Rhonda R, MacKenzie-Graham Allan
UCLA MS Program, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Front Mol Neurosci. 2022 Oct 19;15:1024058. doi: 10.3389/fnmol.2022.1024058. eCollection 2022.
Animal models of multiple sclerosis (MS), specifically experimental autoimmune encephalomyelitis (EAE), have been used extensively to develop anti-inflammatory treatments. However, the similarity between MS and one particular EAE model does not end at inflammation. MS and chronic EAE induced in C57BL/6 mice using myelin oligodendrocyte glycoprotein (MOG) peptide 35-55 share many neuropathologies. Beyond both having white matter lesions in spinal cord, both also have widespread neuropathology in the cerebral cortex, hippocampus, thalamus, striatum, cerebellum, and retina/optic nerve. In this review, we compare neuropathologies in each of these structures in MS with chronic EAE in C57BL/6 mice, and find evidence that this EAE model is well suited to study neuroaxonal degeneration in MS.
多发性硬化症(MS)的动物模型,特别是实验性自身免疫性脑脊髓炎(EAE),已被广泛用于开发抗炎治疗方法。然而,MS与一种特定EAE模型之间的相似性并不局限于炎症。使用髓鞘少突胶质细胞糖蛋白(MOG)肽35 - 55在C57BL/6小鼠中诱导的MS和慢性EAE具有许多神经病理学特征。除了脊髓都有白质病变外,两者在大脑皮层、海马体、丘脑、纹状体、小脑以及视网膜/视神经中也都存在广泛的神经病理学变化。在本综述中,我们将MS中这些结构的神经病理学与C57BL/6小鼠的慢性EAE进行比较,并发现证据表明该EAE模型非常适合研究MS中的神经轴突退化。