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dc.contributor.authorPerer, Jessica
dc.contributor.authorJandova, Jana
dc.contributor.authorFimbres, Jocelyn
dc.contributor.authorJennings, Erin Q.
dc.contributor.authorGalligan, James J.
dc.contributor.authorHua, Anh
dc.contributor.authorWondrak, Georg T.
dc.date.accessioned2021-04-03T01:36:07Z
dc.date.available2021-04-03T01:36:07Z
dc.date.issued2020-09
dc.identifier.citationPerer, J., Jandova, J., Fimbres, J., Jennings, E. Q., Galligan, J. J., Hua, A., & Wondrak, G. T. (2020). The sunless tanning agent dihydroxyacetone induces stress response gene expression and signaling in cultured human keratinocytes and reconstructed epidermis. Redox Biology, 36, 101594.
dc.identifier.issn2213-2317
dc.identifier.pmid32506039
dc.identifier.doi10.1016/j.redox.2020.101594
dc.identifier.urihttp://hdl.handle.net/10150/657589
dc.description.abstractSunless (chemical) tanning is widely regarded as a safe alternative to solar UV-induced skin tanning known to be associated with epidermal genotoxic stress, but the cutaneous biology impacted by chemical tanning remains largely unexplored. Chemical tanning is based on the formation of melanin-mimetic cutaneous pigments ('melanoidins') from spontaneous amino-carbonyl ('glycation') reactions between epidermal amino acid/protein components and reactive sugars including the glycolytic ketose dihydroxyacetone (DHA). Here, we have examined the cutaneous effects of acute DHA-exposure on cultured human HaCaT keratinocytes and epidermal reconstructs, profiled by gene expression array analysis and immunodetection. In keratinocytes, DHA-exposure performed at low millimolar concentrations did not impair viability while causing a pronounced cellular stress response as obvious from rapid activation of phospho-protein signal transduction [p-p38, p-Hsp27(S15/S78), p-elF2a] and gene expression changes (HSPA6, HMOX1, CRYAB, CCL3), not observable upon exposure to the nonketose, tanning-inactive DHA-control glycerol. Formation of advanced glycation end products (AGEs) from posttranslational protein-adduction was confirmed by quantitative mass spectrometric detection of N-E-(carboxyethyl)-L-lysine (CEL) and N-7 -carboxyethyl-L-arginine, and skin cells with CRISPR-Cas9-based elimination of the carbonyl stress response gene GLO1 (encoding glyoxalase 1) displayed hypersensitivity to DHA-cytotoxicity. In human epidermal reconstructs a topical use-relevant DHA-dose regimen elicited a comparable stress response as revealed by gene expression array (HSPAIA, HSPA6, HSPD1, 1L6, DDIT3, EGR1) and immunohistochemical analysis (CEL, HO-1, p-Hsp27-S78). In DHA-treated SKH-1 hairless mouse skin IHC-detection revealed epidermal occurrence of CEL- and p-Hsp27-epitopes. For comparison, stress response gene expression array analysis was performed in epidermis exposed to a supra-erythemal dose of solar simulated UV (2 MEDs), identifying genes equally or differentially sensitive to either one of these cutaneous stimuli [DHA ('sunless tanning') versus solar UV ('sun-induced tanning')]. Given the worldwide use of chemical tanners in consumer products, these prototype data documenting a DHA-induced specific cutaneous stress response deserve further molecular exploration in living human skin.
dc.language.isoen
dc.publisherELSEVIER
dc.rights© 2020 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectSunless tanning
dc.subjectDihydroxyacetone
dc.subjectGlycation
dc.subjectReconstructed human epidermis
dc.subjectStress response gene expression
dc.subjectPhosphoprotein signaling
dc.titleThe sunless tanning agent dihydroxyacetone induces stress response gene expression and signaling in cultured human keratinocytes and reconstructed epidermis
dc.typeArticle
dc.typetext
dc.contributor.departmentUniv Arizona, Coll Pharm, Dept Pharmacol & Toxicol
dc.contributor.departmentUniv Arizona, UA Canc Ctr
dc.identifier.journalREDOX BIOLOGY
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal published version
dc.source.journaltitleREDOX BIOLOGY
refterms.dateFOA2021-04-03T01:36:07Z


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© 2020 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as © 2020 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).