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首页> 外文期刊>DNA and Cell Biology >The Molecular Basis of Copper Homeostasis Copper-Related Disorders
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The Molecular Basis of Copper Homeostasis Copper-Related Disorders

机译:铜稳态与铜相关疾病的分子基础

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摘要

Copper is an essential trace element that can be extremely toxic in excess due to the pro-oxidant activity of copper ions. Inherited disorders of copper transport, Menkes disease (copper deficiency), and Wilson disease (copper toxicosis) are caused by mutations of two closely related Cu transporting-ATPases, and demonstrate the essentiality and potential toxicity of copper. Other copper toxicosis conditions in humans and animals have been described, but are not well understood at a molecular level. Copper homeostatic mechanisms are being discovered. One such mechanism is copper-induced trafficking of the Cu-ATPases, which allows cells to provide copper to secreted cupro-proteins but also to efflux excess copper. Oxidative damage induced by copper may be involved in the pathogenesis of neurodegenerative conditions such as Alzheimer's disease, familial amyotrophic lateral sclerosis, and prion diseases.
机译:铜是必需的微量元素,由于铜离子的促氧化活性,其毒性可能极高。铜运输的遗传性疾病,Menkes病(铜缺乏症)和Wilson病(铜中毒)是由两个紧密相关的Cu转运性ATPase的突变引起的,证明了铜的必要性和潜在毒性。已经描述了人和动物中的其他铜中毒情况,但在分子水平上尚不为人所知。铜稳态机制正在被发现。一种这样的机制是铜诱导的Cu-ATPase的运输,它使细胞可以为分泌的铜蛋白提供铜,但也可以排出过量的铜。铜引起的氧化损伤可能与神经退行性疾病的发病机制有关,例如阿尔茨海默氏病,家族性肌萎缩性侧索硬化症和病毒病。

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