Most mammalian tissue cells experience oxygen partial pressures equivalent to 1-6% O (i.e., physioxia). In standard cell culture, however, headspace O levels are usually not actively regulated and under these conditions are ~18%. This drives hyperoxia in cell culture media that can affect a wide variety of cellular activities and may compromise the ability of models to reproduce biology. Here, we review and discuss some specific O-consuming organelles and enzymes, including mitochondria, NADPH oxidases, the transplasma membrane redox system, nitric oxide synthases, xanthine oxidase, and monoamine oxidase with respect to their sensitivities to O levels. Many of these produce reactive oxygen and/or nitrogen species (ROS/RNS) as either primary end products or byproducts and are acutely sensitive to O levels in the range from 1% to 18%. Interestingly, many of them are also transcriptional targets of hypoxia-inducible factors (HIFs) and chronic cell growth at physioxia versus 18% O may alter their expression. Aquaporins, which facilitate hydrogen peroxide diffusion into and out of cells, are also regulated by HIFs, indicating that O levels may affect intercellular communication via hydrogen peroxide. The O sensitivities of these important activities emphasize the importance of maintaining physioxia in culture.
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http://dx.doi.org/10.1155/2018/8238459 | DOI Listing |
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Department of Bioengineering, University of California, Riverside, 900 University Avenue, Riverside, California 92521, United States.
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School of Bioengineering, East China University of Science and Technology, Shanghai, China.
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