4.5 Article

Mouse redox histology using genetically encoded probes

Journal

SCIENCE SIGNALING
Volume 9, Issue 419, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scisignal.aad3895

Keywords

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Funding

  1. DFG (Deutsche Forschungsgemeinschaft) [SFB1036, SFB938, SPP1710]
  2. BMBF (Federal Ministry of Education and Research) (LungSysII)
  3. Helmholtz Cross-Program topic Metabolic Dysfunction
  4. ICEMED (Imaging and Curing Environmental Metabolic Diseases) alliance
  5. DFG [EXC 1010, SFB-Tr 128, SPP 1710, EXC 114, SFB 870]
  6. European Research Council (ERC) [310932]
  7. European Research Council under the European Union [616791]
  8. German Cancer Research Center (DKFZ)
  9. Japan Society for the Promotion of Science
  10. Sao Paulo Research Foundation (FAPESP)
  11. DKFZ visiting scientist program
  12. Boehringer Ingelheim Fonds
  13. Medical Faculty, University of Heidelberg
  14. European Research Council (ERC) [616791, 310932] Funding Source: European Research Council (ERC)

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Mapping the in vivo distribution of endogenous oxidants in animal tissues is of substantial biomedical interest. Numerous health-related factors, including diet, physical activity, infection, aging, toxins, or pharmacological intervention, may cause redox changes. Tools are needed to pinpoint redox state changes to particular organs, tissues, cell types, and subcellular organelles. We describe a procedure that preserves the in vivo redox state of genetically encoded redox biosensors within histological tissue sections, thus providing redox maps for any tissue and comparison of interest. We demonstrate the utility of the technique by visualizing endogenous redox differences and changes in the context of tumor growth, inflammation, embryonic development, and nutrient starvation.

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