Stankovic Roger K, Chung Roger S, Penkowa Milena
Department of Pathology, University of Sydney, NSW, Australia.
Int J Biochem Cell Biol. 2007;39(3):484-9. doi: 10.1016/j.biocel.2006.09.010. Epub 2006 Oct 10.
Metallothioneins (MTs) constitutes a superfamily of highly conserved, low molecular weight polypeptides, which are characterized by high contents of cysteine (sulphur) and metals. As intracellular metal-binding proteins they play a significant role in the regulation of essential metals. The major isoforms of the protein (MT-I and MT-II) are induced by numerous stimuli and pathogens but most importantly their induction by metals is closely linked to the physiological metabolism of zinc and protection from the toxic affects following heavy metal exposure. Although the preservation of their genetic expression across animal phyla suggests that MTs may play an important physiological role, MT-I, II knock out (KO) mice survive to adulthood. In both central and peripheral nervous tissues, MT-I, II have neuroprotective roles, which are also induced by exogenous MT-I and/or MT-II treatment. Hence, MT-I, II may provide neurotherapeutic targets offering protection against neuronal injury and degeneration.
金属硫蛋白(MTs)构成了一个高度保守的低分子量多肽超家族,其特点是半胱氨酸(硫)和金属含量高。作为细胞内金属结合蛋白,它们在必需金属的调节中发挥着重要作用。该蛋白的主要异构体(MT-I和MT-II)由多种刺激和病原体诱导,但最重要的是,它们由金属诱导与锌的生理代谢以及免受重金属暴露后的毒性影响密切相关。尽管它们在动物门中的基因表达得以保留表明MTs可能发挥重要的生理作用,但MT-I、II基因敲除(KO)小鼠能存活至成年。在中枢和外周神经组织中,MT-I、II具有神经保护作用,外源性MT-I和/或MT-II处理也可诱导这种作用。因此,MT-I、II可能提供神经治疗靶点,为神经元损伤和退化提供保护。