The sunburn response in human skin is characterized by sequential eicosanoid profiles that may mediate its early and late phases
Autor: | Anna Nicolaou, Anthony J. Thody, Desmond J. Tobin, Ann K. Haylett, Mojgan Masoodi, Lesley E. Rhodes, M Brownrigg, K Gledhill |
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Rok vydání: | 2009 |
Předmět: |
Male
CD3 Complex Erythema Lipoxygenase Sunburn Human skin Pharmacology Dinoprost Biochemistry Research Communications prostaglandins hydroxyeicosatetraenoic acids 030207 dermatology & venereal diseases 0302 clinical medicine Tandem Mass Spectrometry Skin 0303 health sciences integumentary system biology Chemistry Hydroxyeicosatetraenoic acid Middle Aged 3. Good health cyclooxygenase Neutrophil Infiltration Female lipids (amino acids peptides and proteins) medicine.symptom Biotechnology Adult Spectrometry Mass Electrospray Ionization leukocytes Ultraviolet Rays Inflammation Dinoprostone Proinflammatory cytokine 03 medical and health sciences Genetics medicine Humans Alprostadil Molecular Biology 030304 developmental biology Eicosanoid Cyclooxygenase 2 Immunology biology.protein Eicosanoids Cyclooxygenase |
Zdroj: | The FASEB Journal |
ISSN: | 1530-6860 0892-6638 |
DOI: | 10.1096/fj.09-136077 |
Popis: | Sunburn is a commonly occurring acute inflammatory process, with dermal vasodilatation and leukocyte infiltration as central features. Ultraviolet (UV) B-induced hydrolysis of membrane phospholipids releases polyunsaturated fatty acids, and their subsequent metabolism by cyclooxygenases (COXs) and lipoxygenases (LOXs) may produce potent eicosanoid mediators modulating different stages of the inflammation. Our objective was to identify candidate eicosanoids formed during the sunburn reaction in relation to its clinical and histological course. We exposed skin of healthy humans (n=32) to UVB and, for 72 h, examined expression of proinflammatory and anti-inflammatory eicosanoids using LC/ESI-MS/MS, and examined immunohistochemical expression of COX-2, 12-LOX, 15-LOX, and leukocyte markers, while quantifying clinical erythema. We show that vasodilatory prostaglandins (PGs) PGE2, PGF2α, and PGE3 accompany the erythema in the first 24–48 h, associated with increased COX-2 expression at 24 h. Novel, potent leukocyte chemoattractants 11-, 12-, and 8-monohydroxy-eicosatetraenoic acid (HETE) are elevated from 4 to 72 h, in association with peak dermal neutrophil influx at 24 h, and increased dermal CD3+ lymphocytes and 12- and 15-LOX expression from 24 to 72 h. Anti-inflammatory metabolite 15-HETE shows later expression, peaking at 72 h. Sunburn is characterized by overlapping sequential profiles of increases in COX products followed by LOX products that may regulate subsequent events and ultimately its resolution.—Rhodes, L. E., Gledhill, K., Masoodi, M., Haylett, A. K., Brownrigg, M., Thody, A. J., Tobin, D. J., Nicolaou, A. The sunburn response in human skin is characterized by sequential eicosanoid profiles that may mediate its early and late phases. |
Databáze: | OpenAIRE |
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