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Release of Inflammatory Mediators (PGE 2 , IL‐6) by Fenofibric Acid‐Photosensitized Human Keratinocytes and Fibroblasts
Author(s) -
Terencio Mari Carmen,
Guillen Isabel,
GomezLechon Marfa Jose,
Miranda Miguel A.,
Castell Jose V.
Publication year - 1998
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1998.tb09690.x
Subject(s) - phototoxicity , chemistry , cytokine , in vivo , proinflammatory cytokine , human skin , keratinocyte , metabolite , cell culture , stimulation , pharmacology , in vitro , biochemistry , biophysics , microbiology and biotechnology , inflammation , immunology , biology , endocrinology , genetics
Ultraviolet‐A radiation has weak effects on the release of inflammatory mediators by skin cells due to the poor overlap between UVA wavelengths and the absorption spectra of the relevant chromophores of key biomole‐cules. However, this situation could be very different in the presence of a photosensitizing drug. To investigate this issue, we have irradiated human skin cells (keratinocytes and fibroblasts) in the presence of fenofibric acid (the active phototoxic metabolite of fenofibrate). The results of this research show a dual effect on the production/release of inflammatory mediators: the synthesis of the proinflammatory cytokine interleukin‐6 becomes strongly inhibited at photosensitizer concentrations that clearly stimulate the production of prostaglandins (PGE 2 ) by skin cells. We have found evidences showing that the de novo synthesis of cytokines is inhibited in photosensitized cells due to the fact that cellular mRNA is degraded. Interestingly, when the medium taken from irradiated cultures is added to nonexposed cells, a significant stimulation of cytokine synthesis is observed that can be inhibited by anti‐PGE 2 antibodies. These observations may be relevant in vivo , where prostaglandins released by photosensitized skin cells could stimulate cytokine synthesis by underlying, nonirradiated cells.