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Molecular Mechanisms of Photoaging in Human Skin In Vivo and Their Prevention by All‐Trans Retinoic Acid
Author(s) -
Fisher Gary J.,
Talwar Harvinder S.,
Lin Jiayuh,
Voorhees John J.
Publication year - 1999
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.1751-1097.1999.tb03268.x
Subject(s) - photoaging , human skin , phosphorylation , matrix metalloproteinase , retinoic acid , chemistry , microbiology and biotechnology , in vivo , ubiquitin , dephosphorylation , biochemistry , biology , gene , phosphatase , genetics
— Solar UV radiation damages human skin, affecting skin tone and resiliency and leading to premature aging (photoaging), the symptoms of which include leathery texture, wrinkles, mottled pigmentation, laxity and sallowness. We propose that photoaging results largely from UV induction of matrix metalloproteinases (MMP) that degrade skin collagen. We find that pretreatment of human skin with all‐ trans retinoic acid (tRA) inhibits UV induction of MMP, suggesting that tRA can protect against UV‐induced collagen destruction and may therefore be able to lessen the effects of photoaging. The tRA prevents UV‐induced accumulation of c‐Jun protein, which is required for MMP gene expression. Activation of c‐Jun transcriptional activity requires N‐terminal phosphorylation. The majority of c‐Jun in human skin in vivo is Nterminal phosphorylated. Topically applied t RA does not inhibit N‐terminal phosphorylation by UV‐induced c‐Jun kinase activity in human skin. The tRA likely acts to reduce UV induction of c‐Jun protein by stimulating its breakdown through the ubiquitin‐proteasome pathway.