Jürgen Baier, Tim Maisch, Max Maier, Eva Engl, Michael Landthaler, and Wolfgang Bäumler
(J. Baier, T. Maisch,  M. Maier, E. Engl, M. Landthaler, and W. Bäumler)

Journal of Investigative Dermatology advance online publication 15 March 2007

doi: 10.1038/sj.jid.5700741

Abstract:
UVA light produces deleterious biological effects in which singlet oxygen plays a major role. These effects comprise a significant risk of carcinogenesis in the skin and cataract formation of the eye lens. Singlet oxygen is generated by UVA light absorption in endogenous molecules present in the cells. To elucidate the primary processes and sources of singlet oxygen in tissue, it is a major goal to uncover the hidden process of singlet oxygen generation, in particular in living tissue. When exposing keratinocytes or human skin in vivo to UVA laser light (355 nm) at 6 J/cm2, we measured the luminescence of singlet oxygen at 1,270 nm. This is a positive and direct proof of singlet oxygen generation in cells and skin by UVA light. Moreover, a clear signal of singlet oxygen luminescence was detected in phosphatidylcholine suspensions (water or ethanol) irradiated by UVA. Oxidized products of phosphatidylcholine are the likely chromophores because phosphatidylcholine itself does not absorb at 355 nm. The signal intensity was reduced by mannitol or super oxide dismutase. Additionally, the monochromatic UVA irradiation at 355 nm leads to upregulation of the key cytokine IL-12. This affects the balance of UV radiation on the immune system, which is comparable to effects of broadband UVA irradiation.

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