Monitoring cytosolic H2O2 fluctuations arising from altered plasma membrane gradients or from mitochondrial activity

被引:35
作者
Carmona, Merce [1 ]
de Cubas, Laura [1 ]
Bautista, Eric [1 ]
Moral-Blanch, Marta [1 ]
Medrano-Fernandez, Iria [2 ]
Sitia, Roberto [2 ]
Boronat, Susanna [1 ]
Ayte, Jose [1 ]
Hidalgo, Elena [1 ]
机构
[1] Univ Pompeu Fabra, OXidat Stress & Cell Cycle Grp, C Dr Aiguader 88, Barcelona 08003, Spain
[2] Univ Vita Salute San Raffaele, Osped San Raffaele, IRCCS, Prot Transport & Secret Unit,Div Genet & Cell Bio, I-20132 Milan, Italy
关键词
SCHIZOSACCHAROMYCES-POMBE; HYDROGEN-PEROXIDE; TRANSCRIPTION FACTOR; FISSION YEAST; REDOX; PEROXIREDOXIN; METABOLISM; ACTIVATION; EXPRESSION; STRESS;
D O I
10.1038/s41467-019-12475-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genetically encoded probes monitoring H2O2 fluctuations in living organisms are key to decipher redox signaling events. Here we use a new probe, roGFP2-Tpx1.C169S, to monitor pre-toxic fluctuations of peroxides in fission yeast, where the concentrations linked to signaling or to toxicity have been established. This probe is able to detect nanomolar fluctuations of intracellular H2O2 caused by extracellular peroxides; expression of human aquaporin 8 channels H2O2 entry into fission yeast decreasing membrane gradients. The probe also detects H2O2 bursts from mitochondria after addition of electron transport chain inhibitors, the extent of probe oxidation being proportional to the mitochondrial activity. The oxidation of this probe is an indicator of steady-state levels of H2O2 in different genetic backgrounds. Metabolic reprogramming during growth in low-glucose media causes probe reduction due to the activation of antioxidant cascades. We demonstrate how peroxiredoxin-based probes can be used to monitor physiological H2O2 fluctuations.
引用
收藏
页数:13
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