New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry.
Ana ReulaDaniel PellicerSilvia Castillo-CorullonMaría MagallónMiguel Armengot-CarcellerGuadalupe HerreraJosé-Enrique O'ConnorLucía BañulsMaría Mercedes Navarro-GarcíaAmparo EscribanoFrancisco DasíPublished in: Journal of clinical medicine (2021)
Several studies have shown the importance of oxidative stress (OS) in respiratory disease pathogenesis. It has been reported that the nasal epithelium may act as a surrogate for the bronchial epithelium in several respiratory diseases involving OS. However, the sample yields obtained from nasal biopsies are modest, limiting the number of parameters that can be determined. Flow cytometry has been widely used to evaluate cellular OS profiles. It has the advantage that analyses can be performed using a small amount of sample. Therefore, we aimed to set up a new method based on flow cytometry to assess the oxidative profile of human nasal epithelial cells which could be used in research on respiratory diseases. Levels of total nitric oxide, superoxide anion, peroxynitrite, and intracellular peroxides were measured. Reduced thiol levels, such as antioxidant-reduced glutathione and oxidative damaged lipids and proteins, were also analysed. The intracellular calcium levels, plasma membrane potential, apoptosis, and percentage of live cells were also studied. Finally, a strategy to evaluate the mitochondrial function, including mitochondrial hydrogen peroxide, superoxide anion, mitochondrial mass, and membrane potential, was set up. Using small amounts of sample and a non-invasive sampling technique, the described method enables the measurement of a comprehensive set of OS parameters in nasal epithelial cells, which could be useful in research on respiratory diseases.
Keyphrases
- flow cytometry
- oxidative stress
- hydrogen peroxide
- nitric oxide
- induced apoptosis
- chronic rhinosinusitis
- endothelial cells
- ischemia reperfusion injury
- diabetic rats
- dna damage
- cell cycle arrest
- randomized controlled trial
- endoplasmic reticulum stress
- induced pluripotent stem cells
- pluripotent stem cells
- reactive oxygen species
- ionic liquid
- cell death
- anti inflammatory
- climate change
- cell proliferation
- living cells