AIMS: Reactive oxygen species (ROS) and downstream redox alterations not only mediate physiological signaling but also neuropathology. For long, ROS/redox imaging was hampered by a lack of reliable probes. Genetically encoded redox sensors overcame this gap and revolutionized (sub)cellular redox imaging. Yet, the successful delivery of sensor-coding DNA, which demands transfection/transduction of cultured preparations or stereotaxic microinjections of each subject, remains challenging. By generating transgenic mice, we aimed to overcome limiting cultured preparations, circumvent surgical interventions, and to extend effectively redox imaging to complex and adult preparations. RESULTS: Our redox indicator mice widely express Thy1-driven roGFP1 (reduction-oxidation-sensitive green fluorescent protein 1) in neuronal cytosol or mitochondria. Negative phenotypic effects of roGFP1 were excluded and its proper targeting and functionality confirmed. Redox mapping by ratiometric wide-field imaging reveals most oxidizing conditions in CA3 neurons. Furthermore, mitochondria are more oxidized than cytosol. Cytosolic and mitochondrial roGFP1s reliably report cell endogenous redox dynamics upon metabolic challenge or stimulation. Fluorescence lifetime imaging yields stable, but marginal, response ranges. We therefore developed automated excitation ratiometric 2-photon imaging. It offers superior sensitivity, spatial resolution, and response dynamics. INNOVATION AND CONCLUSION: Redox indicator mice enable quantitative analyses of subcellular redox dynamics in a multitude of preparations and at all postnatal stages. This will uncover cell- and compartment-specific cerebral redox signals and their defined alterations during development, maturation, and aging. Cross-breeding with other disease models will reveal molecular details on compartmental redox homeostasis in neuropathology. Combined with ratiometric 2-photon imaging, this will foster our mechanistic understanding of cellular redox signals in their full complexity. Antioxid. Redox Signal. 25, 41-58.
AIMS: Reactive oxygen species (ROS) and downstream redox alterations not only mediate physiological signaling but also neuropathology. For long, ROS/redox imaging was hampered by a lack of reliable probes. Genetically encoded redox sensors overcame this gap and revolutionized (sub)cellular redox imaging. Yet, the successful delivery of sensor-coding DNA, which demands transfection/transduction of cultured preparations or stereotaxic microinjections of each subject, remains challenging. By generating transgenic mice, we aimed to overcome limiting cultured preparations, circumvent surgical interventions, and to extend effectively redox imaging to complex and adult preparations. RESULTS: Our redox indicator mice widely express Thy1-driven roGFP1 (reduction-oxidation-sensitive green fluorescent protein 1) in neuronal cytosol or mitochondria. Negative phenotypic effects of roGFP1 were excluded and its proper targeting and functionality confirmed. Redox mapping by ratiometric wide-field imaging reveals most oxidizing conditions in CA3 neurons. Furthermore, mitochondria are more oxidized than cytosol. Cytosolic and mitochondrial roGFP1s reliably report cell endogenous redox dynamics upon metabolic challenge or stimulation. Fluorescence lifetime imaging yields stable, but marginal, response ranges. We therefore developed automated excitation ratiometric 2-photon imaging. It offers superior sensitivity, spatial resolution, and response dynamics. INNOVATION AND CONCLUSION: Redox indicator mice enable quantitative analyses of subcellular redox dynamics in a multitude of preparations and at all postnatal stages. This will uncover cell- and compartment-specific cerebral redox signals and their defined alterations during development, maturation, and aging. Cross-breeding with other disease models will reveal molecular details on compartmental redox homeostasis in neuropathology. Combined with ratiometric 2-photon imaging, this will foster our mechanistic understanding of cellular redox signals in their full complexity. Antioxid. Redox Signal. 25, 41-58.
Authors: Colette T Dooley; Timothy M Dore; George T Hanson; W Coyt Jackson; S James Remington; Roger Y Tsien Journal: J Biol Chem Date: 2004-02-25 Impact factor: 5.157
Authors: Anna E Dikalova; Alfiya T Bikineyeva; Klaudia Budzyn; Rafal R Nazarewicz; Louise McCann; William Lewis; David G Harrison; Sergey I Dikalov Journal: Circ Res Date: 2010-05-06 Impact factor: 17.367
Authors: Vladimir L Kolossov; Bryan Q Spring; Anna Sokolowski; John E Conour; Robert M Clegg; Paul J A Kenis; H Rex Gaskins Journal: Exp Biol Med (Maywood) Date: 2008-02
Authors: Anatoly Samoylenko; Jubayer Al Hossain; Daniela Mennerich; Sakari Kellokumpu; Jukka Kalervo Hiltunen; Thomas Kietzmann Journal: Antioxid Redox Signal Date: 2013-04-15 Impact factor: 8.401
Authors: Qian Chen; Joseph Cichon; Wenting Wang; Li Qiu; Seok-Jin R Lee; Nolan R Campbell; Nicholas Destefino; Michael J Goard; Zhanyan Fu; Ryohei Yasuda; Loren L Looger; Benjamin R Arenkiel; Wen-Biao Gan; Guoping Feng Journal: Neuron Date: 2012-10-17 Impact factor: 17.173
Authors: Edward Avezov; Benedict C S Cross; Gabriele S Kaminski Schierle; Mikael Winters; Heather P Harding; Eduardo Pinho Melo; Clemens F Kaminski; David Ron Journal: J Cell Biol Date: 2013-04-15 Impact factor: 10.539
Authors: Alexander I Kostyuk; Aleksandra D Kokova; Oleg V Podgorny; Ilya V Kelmanson; Elena S Fetisova; Vsevolod V Belousov; Dmitry S Bilan Journal: Antioxidants (Basel) Date: 2020-06-11
Authors: Alexander I Kostyuk; Anastasiya S Panova; Aleksandra D Kokova; Daria A Kotova; Dmitry I Maltsev; Oleg V Podgorny; Vsevolod V Belousov; Dmitry S Bilan Journal: Int J Mol Sci Date: 2020-10-31 Impact factor: 5.923
Authors: Saranya Radhakrishnan; Jacob Norley; Stefan Wendt; Nathan LeRoy; Hana Hall; Stevie Norcross; Sara Doan; Jordan Snaider; Brian A MacVicar; Vikki M Weake; Libai Huang; Mathew Tantama Journal: ACS Chem Neurosci Date: 2020-08-21 Impact factor: 4.418
Authors: Niamh M C Connolly; Pierre Theurey; Vera Adam-Vizi; Nicolas G Bazan; Paolo Bernardi; Juan P Bolaños; Carsten Culmsee; Valina L Dawson; Mohanish Deshmukh; Michael R Duchen; Heiko Düssmann; Gary Fiskum; Maria F Galindo; Giles E Hardingham; J Marie Hardwick; Mika B Jekabsons; Elizabeth A Jonas; Joaquin Jordán; Stuart A Lipton; Giovanni Manfredi; Mark P Mattson; BethAnn McLaughlin; Axel Methner; Anne N Murphy; Michael P Murphy; David G Nicholls; Brian M Polster; Tullio Pozzan; Rosario Rizzuto; Jorgina Satrústegui; Ruth S Slack; Raymond A Swanson; Russell H Swerdlow; Yvonne Will; Zheng Ying; Alvin Joselin; Anna Gioran; Catarina Moreira Pinho; Orla Watters; Manuela Salvucci; Irene Llorente-Folch; David S Park; Daniele Bano; Maria Ankarcrona; Paola Pizzo; Jochen H M Prehn Journal: Cell Death Differ Date: 2017-12-11 Impact factor: 15.828