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慢性实验性自身免疫性脑脊髓炎是研究多发性硬化症中神经轴突退变的极佳模型。

Chronic experimental autoimmune encephalomyelitis is an excellent model to study neuroaxonal degeneration in multiple sclerosis.

作者信息

Voskuhl Rhonda R, MacKenzie-Graham Allan

机构信息

UCLA MS Program, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.

出版信息

Front Mol Neurosci. 2022 Oct 19;15:1024058. doi: 10.3389/fnmol.2022.1024058. eCollection 2022.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c38/9629273/8236d015d4ff/fnmol-15-1024058-g001.jpg

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