Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Exp Biol Med (Maywood). 2014 Apr;239(4):394-403. doi: 10.1177/1535370214522179. Epub 2014 Feb 28.
The glutathione couple GSH/GSSG is the most abundant cellular redox buffer and is not at equilibrium among intracellular compartments. Perturbation of glutathione poise has been associated with tumorigenesis; however, due to analytical limitations, the underlying mechanisms behind this relationship are poorly understood. In this regard, we have implemented a ratiometric, genetically encoded redox-sensitive green fluorescent protein fused to human glutaredoxin (Grx1-roGFP2) to monitor real-time glutathione redox potentials in the cytosol and mitochondrial matrix of tumorigenic and non-tumorigenic cells. First, we demonstrated that recovery time in both compartments depended upon the length of exposure to oxidative challenge with diamide, a thiol-oxidizing agent. We then monitored changes in glutathione poise in cytosolic and mitochondrial matrices following inhibition of glutathione (GSH) synthesis with L-buthionine sulphoximine (BSO). The mitochondrial matrix showed higher oxidation in the BSO-treated cells indicating distinct compartmental alterations in redox poise. Finally, the contributory role of the p53 protein in supporting cytosolic redox poise was demonstrated. Inactivation of the p53 pathway by expression of a dominant-negative p53 protein sensitized the cytosol to oxidation in BSO-treated tumor cells. As a result, both compartments of PF161-T+p53(DD) cells were equally oxidized ≈20 mV by inhibition of GSH synthesis. Conversely, mitochondrial oxidation was independent of p53 status in GSH-deficient tumor cells. Taken together, these findings indicate different redox requirements for the glutathione thiol/disulfide redox couple within the cytosol and mitochondria of resting cells and reveal distinct regulation of their redox poise in response to inhibition of glutathione biosynthesis.
谷胱甘肽二聚体 GSH/GSSG 是细胞内最丰富的氧化还原缓冲剂,在细胞内隔室之间并不处于平衡状态。谷胱甘肽平衡的扰乱与肿瘤发生有关;然而,由于分析上的限制,这种关系背后的潜在机制还了解甚少。在这方面,我们已经实施了一种比率型、基因编码的氧化还原敏感绿色荧光蛋白融合到人谷胱甘肽还原酶(Grx1-roGFP2),以监测肿瘤发生和非肿瘤细胞的细胞质和线粒体基质中谷胱甘肽氧化还原电势的实时变化。首先,我们证明了在两个隔室中的恢复时间取决于用二酰胺(一种硫醇氧化剂)暴露于氧化应激的时间长度。然后,我们监测了谷胱甘肽(GSH)合成被 L-丁硫氨酸亚砜亚胺(BSO)抑制后细胞质和线粒体基质中谷胱甘肽平衡的变化。线粒体基质中 BSO 处理的细胞显示出更高的氧化,表明氧化还原平衡的隔室改变明显。最后,证明了 p53 蛋白在支持细胞质氧化还原平衡中的贡献作用。通过表达显性负 p53 蛋白使 p53 途径失活,使 BSO 处理的肿瘤细胞中的细胞质对氧化更为敏感。结果,PF161-T+p53(DD) 细胞的两个隔室在 GSH 合成抑制下被同样氧化 ≈20 mV。相反,在 GSH 缺乏的肿瘤细胞中,线粒体氧化与 p53 状态无关。总之,这些发现表明,在静止细胞的细胞质和线粒体中,谷胱甘肽巯基/二硫键氧化还原对具有不同的氧化还原需求,并揭示了它们的氧化还原平衡在响应 GSH 生物合成抑制时的不同调节。