Cis-urocanic acid, a sunlight-induced immunosuppressive factor, activates immune suppression via the 5-HT2A receptor
- Jeffrey P. Walterscheid*,†,
- Dat X. Nghiem*,†,
- Nasser Kazimi*,
- Leta K. Nutt†,‡,
- David J. McConkey†,‡,
- Mary Norval§, and
- Stephen E. Ullrich*,†,¶
- *Department of Immunology and Center for Cancer Immunology Research and
- ‡Department of Cancer Biology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030;
- †Graduate School of Biomedical Sciences, University of Texas, Houston, TX 77030; and
- §Medical Microbiology, University of Edinburgh Medical School, Edinburgh EH8 9AG, Scotland
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Edited by Richard B. Setlow, Brookhaven National Laboratory, Upton, NY, and approved September 18, 2006 (received for review April 17, 2006)
Abstract
Exposure to UV radiation induces skin cancer and suppresses the immune response. To induce immune suppression, the electromagnetic energy of UV radiation must be absorbed by an epidermal photoreceptor and converted into a biologically recognizable signal. Two photoreceptors have been recognized: DNA and trans-urocanic acid (UCA). Trans-UCA is normally found in the outermost layer of skin and isomerizes to the cis isomer upon exposure to UV radiation. Although UCA was identified as a UV photoreceptor years ago, and many have documented its ability to induce immune suppression, its exact mode of action remains elusive. Particularly vexing has been the identity of the molecular pathway by which cis-UCA mediates immune suppression. Here we provide evidence that cis-UCA binds to the serotonin [5-hydroxytryptamine (5-HT)] receptor with relatively high affinity (K d = 4.6 nM). Anti-cis-UCA antibody precipitates radiolabeled 5-HT, and the binding is inhibited by excess 5-HT and/or excess cis-UCA. Similarly, anti-5-HT antibody precipitates radiolabeled cis-UCA, and the binding is inhibited by excess 5-HT or excess cis-UCA. Calcium mobilization was activated when a mouse fibroblast line, stably transfected with the human 5-HT2A receptor, was treated with cis-UCA. Cis-UCA-induced calcium mobilization was blocked with a selective 5-HT2A receptor antagonist. UV- and cis-UCA-induced immune suppression was blocked by antiserotonin antibodies or by treating the mice with 5-HT2A receptor antagonists. Our findings identify cis-UCA as a serotonin receptor ligand and indicate that the immunosuppressive effects of cis-UCA and UV radiation are mediated by activation of the 5-HT2A receptor.
Footnotes
- ¶To whom correspondence should be addressed at: Department of Immunology/Unit 902, University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030. E-mail: sullrich{at}mdanderson.org
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Author contributions: J.P.W. and D.X.N. contributed equally to this work; J.P.W., D.X.N., and S.E.U. designed research; J.P.W., D.X.N., N.K., L.K.N., D.J.M., and S.E.U. performed research; M.N. contributed new reagents/analytic tools; and J.P.W., D.X.N., M.N., and S.E.U. wrote the paper.
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The authors declare no conflict of interest.
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This article is a PNAS direct submission.
- Abbreviations:
- DTH,
- delayed-type hypersensitivity;
- 5-HT,
- 5-hydroxytryptamine (serotonin);
- PAF,
- platelet activating factor;
- PGE2,
- prostaglandin E2;
- UCA,
- urocanic acid.
- © 2006 by The National Academy of Sciences of the USA
