Dysfunctions of neuronal and glial intermediate filaments in disease

被引:113
|
作者
Liem, Ronald K. H. [1 ]
Messing, Albee [2 ,3 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pathol & Cell Biol, Taub Inst Res Alzheimers Dis & Aging Brain, New York, NY 10032 USA
[2] Univ Wisconsin, Waisman Ctr, Madison, WI 53705 USA
[3] Univ Wisconsin, Dept Comparat Biosci, Madison, WI 53705 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2009年 / 119卷 / 07期
关键词
FIBRILLARY ACIDIC PROTEIN; MARIE-TOOTH-DISEASE; GIANT AXONAL NEUROPATHY; AMYOTROPHIC-LATERAL-SCLEROSIS; SIZED NEUROFILAMENT SUBUNIT; BRAIN-SPECIFIC PROTEINS; ALPHA-B-CRYSTALLIN; CEREBROSPINAL-FLUID; ALEXANDER-DISEASE; MOTOR-NEURONS;
D O I
10.1172/JCI38003
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Intermediate Filaments (IFs) are abundant structures found in most eukaryotic cells, including those in the nervous system. In the CNS, the primary components of neuronal IFs are a-internexin and the neurofilament triplet proteins. In the peripheral nervous system, a fifth neuronal IF protein known as peripherin is also present. IFs in astrocytes are primarily composed of glial fibrillary acidic protein (GFAP), although vimentin is also expressed in immature astrocytes and some mature astrocytes. In this Review, we focus on the IFs of glial cells (primarily GFAP) and neurons as well as their relationship to different neurodegenerative diseases.
引用
收藏
页码:1814 / 1824
页数:11
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