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Iron and glutathione at the crossroad of redox metabolism in neurons

机译:铁和谷胱甘肽在神经元氧化还原代谢的十字路口

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摘要

Neurons, as non-dividing cells, encounter a myriad of stressful conditions throughout their lifespan. In particular, there is increasing evidence that iron progressively accumulates in the brain with age and that iron-induced oxidative stress is the cause of several forms of neurodegeneration. Here, we review recent evidence that gives support to the following notions: 1) neuronal iron accumulation leads to oxidative stress and cell death; 2) neuronal survival to iron accumulation associates with decreased expression of the iron import transporter DMT1 and increased expression of the efflux transporter IREG1; and 3) the adaptive process of neurons towards iron-induced oxidative stress includes a marked increase in both the expression of the catalytic subunit of gamma glutamate-cysteine ligase and glutathione. These findings may help to understand aging-related neurodegeneration hallmarks: oxidative damage, functional impairment and cell death.
机译:神经元作为非分裂细胞,在其整个生命周期中都会遇到无数的压力状态。尤其是,越来越多的证据表明,铁会随着年龄的增长而逐渐在大脑中积累,并且铁诱导的氧化应激是多种形式的神经变性的原因。在这里,我们回顾了支持以下观点的最新证据:1)神经元铁的积累导致氧化应激和细胞死亡。 2)铁累积的神经元存活与铁输入转运蛋白DMT1的表达降低和外排转运蛋白IREG1的表达增加有关; (3)神经元对铁诱导的氧化应激的适应性过程包括γ-谷氨酸-半胱氨酸连接酶和谷胱甘肽的催化亚基表达的显着增加。这些发现可能有助于理解与衰老相关的神经退行性标志:氧化损伤,功能障碍和细胞死亡。

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