Mice, the motor system, and human motor neuron pathology

被引:22
作者
Nicholson, SJ
Witherden, AS
Hafezparast, M
Martin, JE
Fisher, EMC
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Neurogenet, London W2 1PG, England
[2] Queen Mary Univ London, Royal London Hosp, Dept Histopathol, London E1 1BB, England
关键词
D O I
10.1007/s003350010205
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
Motor neurons are among some of the most unusual cells in the body becaue of their immense size and their role as the critical link between the motor centers of the brain and the muscles. In addition to their intrinsic biological interest, it is vital that we gain a better understanding of these cells and their pathology, since motor neuron degenerative diseases are lethal disorders that affect young and old and are relatively common. For example, one form of spinal muscular atrophy (SMA) is the most common genetic killer of children in the developed world. Amyotrophic lateral sclerosis (ALS), another form of motor neuron degeneration, is the third most common neurodegenerative cause of adult death, after Alzheimer's disease and Parkinson's disease, and is significantly more common than multiple sclerosis (Motor Neurone Disease Association 1998). Currently, approximately 1 in 500 people in England and Wares who die have a form of motor neuron disease (Motor Neurone Disease Association 1998). Each year, 5000 Americans are diagnosed with ALS, and of these, 10% are under 40 years old. Mouse models of motor neuron degeneration are essential for understanding the causes and mechanisms of motor neuron pathology. These mice are yielding important information that will ultimately lead to treatments and potentially cures for these diseases.
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收藏
页码:1041 / 1052
页数:12
相关论文
共 138 条
[1]  
Adams RA, 1997, Principles of neurology, V6th
[2]   Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis [J].
Al-Chalabi, A ;
Andersen, PM ;
Nilsson, P ;
Chioza, B ;
Andersson, JL ;
Russ, C ;
Shaw, CE ;
Powell, JF ;
Leigh, PN .
HUMAN MOLECULAR GENETICS, 1999, 8 (02) :157-164
[3]   FINE-STRUCTURE OF CERVICAL SPINAL-CORD, VENTRAL ROOT AND BRACHIAL NERVES IN WOBBLER (WR) MOUSE [J].
ANDREWS, JM .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1975, 34 (01) :12-27
[4]  
[Anonymous], 1992, CENTRAL NERVOUS SYST
[5]   Increased motoneuron survival and improved neuromuscular function in transgenic ALS mice after intraspinal injection of an adeno-associated virus encoding bcl-2 [J].
Azzouz, M ;
Hottinger, A ;
Paterna, JC ;
Zurn, AD ;
Aebischer, P ;
Büeler, H .
HUMAN MOLECULAR GENETICS, 2000, 9 (05) :803-811
[6]   Brain-derived neurotrophic factor fails to arrest neuromuscular disorders in the paralyse mouse mutant, a model of motoneuron disease [J].
Blondet, B ;
Murawsky, M ;
Houenou, LJ ;
Li, LX ;
Aït-Ikhlef, AA ;
Yan, Q ;
Rieger, F .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 153 (01) :20-24
[7]   Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic mice [J].
Borchelt, DR ;
Wong, PC ;
Becher, MW ;
Pardo, CA ;
Lee, MK ;
Xu, ZS ;
Thinakaran, G ;
Jenkins, NA ;
Copeland, NG ;
Sisodia, SS ;
Cleveland, DW ;
Price, DL ;
Hoffman, PN .
NEUROBIOLOGY OF DISEASE, 1998, 5 (01) :27-35
[8]   Mechanisms of selective motor neuron death in ALS: Insights from transgenic mouse models of motor neuron disease [J].
Bruijn, LI ;
Cleveland, DW .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1996, 22 (05) :373-387
[9]   ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions [J].
Bruijn, LI ;
Becher, MW ;
Lee, MK ;
Anderson, KL ;
Jenkins, NA ;
Copeland, NG ;
Sisodia, SS ;
Rothstein, JD ;
Borchelt, DR ;
Price, DL ;
Cleveland, DW .
NEURON, 1997, 18 (02) :327-338
[10]   Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1 [J].
Bruijn, LI ;
Houseweart, MK ;
Kato, S ;
Anderson, KL ;
Anderson, SD ;
Ohama, E ;
Reaume, AG ;
Scott, RW ;
Cleveland, DW .
SCIENCE, 1998, 281 (5384) :1851-1854