Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
J Biol Chem. 2012 Feb 10;287(7):4397-402. doi: 10.1074/jbc.R111.287995. Epub 2011 Dec 6.
Aerobic organisms generate reactive oxygen species as metabolic side products and must achieve a delicate balance between using them for signaling cellular functions and protecting against collateral damage. Small molecule (e.g. glutathione and cysteine)- and protein (e.g. thioredoxin)-based buffers regulate the ambient redox potentials in the various intracellular compartments, influence the status of redox-sensitive macromolecules, and protect against oxidative stress. Less well appreciated is the fact that the redox potential of the extracellular compartment is also carefully regulated and is dynamic. Changes in intracellular metabolism alter the redox poise in the extracellular compartment, and these are correlated with cellular processes such as proliferation, differentiation, and death. In this minireview, the mechanism of extracellular redox remodeling due to intracellular sulfur metabolism is discussed in the context of various cell-cell communication paradigms.
需氧生物作为代谢副产物会产生活性氧物种,它们必须在利用这些物质进行细胞功能信号传递和防止附带损伤之间达到微妙的平衡。小分子(如谷胱甘肽和半胱氨酸)和蛋白(如硫氧还蛋白)为基础的缓冲剂调节各种细胞内隔室中的环境氧化还原电势,影响氧化还原敏感的大分子的状态,并防止氧化应激。不太为人所知的是,细胞外隔室的氧化还原电势也受到仔细调节并且是动态的。细胞内代谢的变化改变了细胞外隔室的氧化还原平衡,这些变化与细胞过程如增殖、分化和死亡相关。在这篇综述中,将根据各种细胞间通讯范例讨论细胞内硫代谢引起细胞外氧化还原重塑的机制。