It is recognized that reactive oxygen species (ROS) are responsible for skin damage due to UVB-radiation (UVB-R). However, the triggering substance(s) for ROS generation after UVB-R is uncertain with respect to the activation of NADPH oxidase (Nox), xanthine oxidase (XOD), and respiratory chain-chain reactions in mitochondria. As a first step in identifying the trigger(s) for UVB-induced ROS generation, we examined the relationship between Ca2+ levels and ROS generation in HaCaT keratinocytes. UVB-R exposure of HaCaT keratinocytes resulted in an immediate elevation of ROS that recurred 7 hours later. This was accompanied by immediately elevated intracellular Ca 2+ . A Ca2+ chelating agent, BAPTA, abolished the elevation of ROS after UVB-R completely. In addition, exogenous H 2O2 did not increase intracellular Ca2+ levels. This suggests that intracellular Ca2+ is the first trigger for UVB-induced ROS generation. © 2009 The Society for Investigative Dermatology.
CITATION STYLE
Masaki, H., Izutsu, Y., Yahagi, S., & Okano, Y. (2009). Reactive oxygen species in HaCaT keratinocytes after UVB irradiation are triggered by intracellular Ca2+ levels. In Journal of Investigative Dermatology Symposium Proceedings (Vol. 14, pp. 50–52). Nature Publishing Group. https://doi.org/10.1038/jidsymp.2009.12
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