The molecular basis of neurodegeneration in multiple sclerosis

被引:230
作者
Lassmann, Hans [1 ]
van Horssen, Jack [2 ]
机构
[1] Med Univ Vienna, Ctr Brain Res, A-1090 Vienna, Austria
[2] Vrije Univ Amsterdam, Med Ctr, Dept Mol Cell Biol & Immunol, NL-1081 BT Amsterdam, Netherlands
关键词
Multiple sclerosis; Neurodegeneration; Inflammation; Oxidative damage; CENTRAL-NERVOUS-SYSTEM; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; CD8(+) T-CELLS; NITRIC-OXIDE SYNTHASE; WHITE-MATTER; OXIDATIVE DAMAGE; ALLERGIC ENCEPHALOMYELITIS; MITOCHONDRIAL DYSFUNCTION; AXONAL DEGENERATION; REACTIVE OXYGEN;
D O I
10.1016/j.febslet.2011.08.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies aimed to elucidate the pathogenesis of the disease and to find new therapeutic options for multiple sclerosis (MS) patients heavily rely on experimental autoimmune encephalomyelitis (EAE) as a suitable experimental model. This strategy has been highly successful for the inflammatory component of the disease, but had so far little success in the development of neuroprotective therapies, which are also effective in the progressive stage of the disease. Here we discuss opportunities and limitations of EAE models for MS research and provide an overview on the complex mechanisms leading to demyelination and neurodegeneration in this disease. We suggest that the underlying mechanisms involve adaptive and innate immunity. However, mitochondrial injury, resulting in energy failure, is a key element of neurodegeneration in MS and is apparently driven by radical production in activated microglia. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3715 / 3723
页数:9
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