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由铜锌超氧化物歧化酶突变引起的家族性肌萎缩侧索硬化症的致病机制

Pathogenic mechanisms in familial amyotrophic lateral sclerosis due to mutation of Cu, Zn superoxide dismutase.

作者信息

Gurney M E, Cutting F B, Zhai P, Andrus P K, Hall E D

机构信息

Central Nervous System Diseases Research Unit, Upjohn Laboratories, Kalamazoo, MI 49001, USA.

出版信息

Pathol Biol (Paris). 1996 Jan;44(1):51-6.

PMID:8734301
Abstract

Oxidative mechanisms of damage have been implicated indirectly in the damage to brain tissue caused acutely by ischemia or chronically by neurodegenerative diseases. A direct link between pathogenesis and antioxidant enzyme systems has come from studies of a genetic form of amyotrophic lateral sclerosis (ALS). ALS causes the degeneration of motor neurons in cortex, brainstem and spinal cord with consequent progressive paralysis and death. The disease occurs in both sporadic and familial forms. Some 20% of kindreds in which ALS is inherited in an autosomal dominant fashion have mutations in the gene (SOD1) encoding Cu, Zn superoxide dismutase (SOD). Several SOD1 mutations have been shown by ourselves and others to cause motor neuron disease when expressed at high levels in transgenic mice, whereas transgenic mice expressing comparable amounts of wild-type human SOD do not show clinical disease. Thus, we have argued that motor neuron disease is caused by gain-of-function mutations in the human SOD1 gene. Our current experiments investigate the link between mutation of SOD1 and oxidative pathways of damage.

摘要

氧化损伤机制已被间接认为与急性缺血或慢性神经退行性疾病所致的脑组织损伤有关。发病机制与抗氧化酶系统之间的直接联系来自对一种遗传性肌萎缩侧索硬化症(ALS)的研究。ALS会导致皮质、脑干和脊髓中的运动神经元退化,进而导致进行性瘫痪和死亡。该疾病有散发性和家族性两种形式。约20%以常染色体显性方式遗传ALS的家族中,编码铜锌超氧化物歧化酶(SOD)的基因(SOD1)发生了突变。我们和其他人已表明,若干SOD1突变在转基因小鼠中高水平表达时会导致运动神经元疾病,而表达相当数量野生型人类SOD的转基因小鼠则未表现出临床疾病。因此,我们认为运动神经元疾病是由人类SOD1基因的功能获得性突变引起的。我们目前的实验研究SOD1突变与氧化损伤途径之间的联系。

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Pathogenic mechanisms in familial amyotrophic lateral sclerosis due to mutation of Cu, Zn superoxide dismutase.由铜锌超氧化物歧化酶突变引起的家族性肌萎缩侧索硬化症的致病机制
Pathol Biol (Paris). 1996 Jan;44(1):51-6.
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Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron disease.人类运动神经元疾病转基因小鼠模型中的氧化应激、突变型超氧化物歧化酶1和神经丝病理学
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[Amyotrophic lateral sclerosis: recent insights from transgenic animal models with SOD1 mutations].[肌萎缩侧索硬化症:SOD1 突变转基因动物模型的最新见解]
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Familial amyotrophic lateral sclerosis.家族性肌萎缩侧索硬化症
Clin Neurosci. 1995;3(6):338-47.

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