Neuronal intermediate filaments and ALS: A new look at an old question

被引:109
作者
Xiao, Shangxi [1 ]
McLean, Jesse [1 ]
Robertson, Janice [1 ]
机构
[1] Univ Toronto, Ctr Res Neurodegenerat Dis, Dept Lab Med & Pathobiol, Toronto, ON M5S 3H2, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2006年 / 1762卷 / 11-12期
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
amyotrophic lateral sclerosis; intermediate filament; neurofilament; peripherin;
D O I
10.1016/j.bbadis.2006.09.003
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
One of the pathological hallmarks of ALS is the presence of axonal spheroids and perikaryal accumulations/aggregations comprised of the neuronal intermediate filament proteins, neurofilaments and peripherin. These abnormalities represent a point of convergence of both familial and sporadic forms of the disease and understanding their formation may reveal shared pathways in what is otherwise considered a highly heterogeneous disorder. Here we provide a review of the basic biology of neurofilaments and peripherin and the evidence linking them with ALS disease pathogenesis. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1001 / 1012
页数:12
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