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实验性自身免疫性脑脊髓炎中中枢神经系统炎症、脱髓鞘和轴突损伤的评分。

Scoring Central Nervous System Inflammation, Demyelination, and Axon Injury in Experimental Autoimmune Encephalomyelitis.

机构信息

Department of Immunology, University of Toronto.

Keenan Research Centre for Biomedical Science of St. Michael's Hospital.

出版信息

J Vis Exp. 2024 Feb 23(204). doi: 10.3791/65738.

DOI:10.3791/65738
PMID:38465945
Abstract

Experimental autoimmune encephalomyelitis (EAE) is a common immune-based model of multiple sclerosis (MS). This disease can be induced in rodents by active immunization with protein components of the myelin sheath and Complete Freund's adjuvant (CFA) or by the transfer of myelin-specific T effector cells from rodents primed with myelin protein/CFA into naïve rodents. The severity of EAE is typically scored on a 5-point clinical scale that measures the degree of ascending paralysis, but this scale is not optimal for assessing the extent of recovery from EAE. For example, clinical scores remain high in some EAE models (e.g., myelin oligodendrocyte glycoprotein [MOG] peptide-induced model of EAE) despite the resolution of inflammation. Thus, it is important to complement clinical scoring with histological scoring of EAE, which also provides a means to study the underlying mechanisms of cellular injury in the central nervous system (CNS). Here, a simple protocol is presented to prepare and stain spinal cord and brain sections from mice and to score inflammation, demyelination, and axonal injury in the spinal cord. The method for scoring leukocyte infiltration in the spinal cord can also be applied to score brain inflammation in EAE. A protocol for measuring soluble neurofilament light (sNF-L) in the serum of mice using a Small Molecule Assay (SIMOA) assay is also described, which provides feedback on the extent of overall CNS injury in live mice.

摘要

实验性自身免疫性脑脊髓炎(EAE)是多发性硬化症(MS)的一种常见免疫基础模型。这种疾病可以通过用髓鞘蛋白和完全弗氏佐剂(CFA)主动免疫或通过用髓鞘蛋白/CFA 预致敏的啮齿动物的髓鞘特异性 T 效应细胞转移到新生啮齿动物中在啮齿动物中诱导。EAE 的严重程度通常根据 5 分临床量表进行评分,该量表测量上行性瘫痪的程度,但该量表并不适合评估 EAE 从恢复的程度。例如,在一些 EAE 模型中(例如,髓鞘少突胶质细胞糖蛋白 [MOG] 肽诱导的 EAE 模型),尽管炎症已经消退,但临床评分仍然很高。因此,用 EAE 的组织学评分补充临床评分很重要,这也为研究中枢神经系统(CNS)中细胞损伤的潜在机制提供了一种手段。此处介绍了一种从小鼠中制备和染色脊髓和脑切片并对脊髓中的炎症、脱髓鞘和轴突损伤进行评分的简单方案。用于评分脊髓中白细胞浸润的方法也可用于评分 EAE 中的脑炎症。还描述了一种使用小分子测定法(SIMOA)测定小鼠血清中可溶性神经丝轻链(sNF-L)的方案,该方案为活小鼠的中枢神经系统损伤程度提供了反馈。

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