"Redox Imaging" to Distinguish Cells with Different Proliferative Indexes: Superoxide, Hydroperoxides, and Their Ratio as Potential Biomarkers.
Zhivko ZhelevEkaterina GeorgievaDessislava LazarovaSeverina SemkovaIchio AokiMaya GulubovaTatsuya HigashiRumiana BakalovaPublished in: Oxidative medicine and cellular longevity (2019)
The present study was directed to the development of EPR methodology for distinguishing cells with different proliferative activities, using "redox imaging." Three nitroxide radicals were used as redox sensors: (a) mito-TEMPO-cell-penetrating and localized mainly in the mitochondria; (b) methoxy-TEMPO-cell-penetrating and randomly distributed between the cytoplasm and the intracellular organelles; and (c) carboxy-PROXYL-nonpenetrating in living cells and evenly distributed in the extracellular environment. The experiments were conducted on eleven cell lines with different proliferative activities and oxidative capacities, confirmed by conventional analytical tests. The data suggest that cancer cells and noncancer cells are characterized by a completely different redox status. This can be analyzed by EPR spectroscopy using mito-TEMPO and methoxy-TEMPO, but not carboxy-PROXYL. The correlation analysis shows that the EPR signal intensity of mito-TEMPO in cell suspensions is closely related to the superoxide level. The described methodology allows the detection of overproduction of superoxide in living cells and their identification based on the intracellular redox status. The experimental data provide evidences about the role of superoxide and hydroperoxides in cell proliferation and malignancy.
Keyphrases
- living cells
- induced apoptosis
- fluorescent probe
- cell cycle arrest
- high resolution
- single cell
- single molecule
- cell proliferation
- endoplasmic reticulum stress
- cell death
- signaling pathway
- reactive oxygen species
- electronic health record
- nitric oxide
- data analysis
- high intensity
- low cost
- photodynamic therapy
- label free