Expression of DUOX2 in Psoriasis and Atopic Dermatitis Lesion
Abstract
To investigate the expression of dual oxidase 2 (DUOX2) in psoriasis vulgaris lesions, atopic dermatitis (AD) lesions and normal skin and its role in cutaneous anti-inflammation. Methods Tissue samples were harvested from psoriasis lesion area, psoriasis non-lesion area, AD lesion area and AD non-lesion area, as well as normal skin, the expression level of DUOX2 protein was detected by immunohistochemical staining. The mRNA level of DUOX2 was detected by reverse transcription polymerase chain reaction (RT-PCR) analysis. Results The expression of DUOX2 protein was observed in all groups which mainly located in basal layer, spinous layer and dermal papilla layer. Compared with the psoriasis non-lesion group and normal skin group, the expression level of DUOX2 protein in psoriasis lesion group was significant higher (P<0.01). The expression of DUOX2 protein in AD lesion group was stronger than that in AD non-lesion group and normal skin group (P<0.01). In addition, the expression level of DUOX2 protein in AD lesion group was significant higher than that in psoriasis lesion group (P<0.01). RT-PCR test revealed DUOX2 mRNA was expressed positively in psoriasis and AD lesions. Conclusion The strong expression of DUOX2 in psoriasis vulgaris lesion and AD lesion suggested that DUOX2 may play an important role in the mechanisms of cutaneous anti-inflammation.
Keywords: Psoriasis, Atopic dermatitis, Dual oxidase 2, Immunohistochemistry, RT-PCR
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Idriss SF, Wolf PD. Transmural action potential repolarization heretogeneity develops postnatally in the rabbit. J Cardiovascular Electrophysiol»2004; 15(7):795-801.
Moss AJ. Long QT syndrome. JAMA, 2003; 289 ( 16 ): 2041- 2044.
Conrath CE, Opthof T. Ventricular repolarization: an overview of (patho)physiology, sympathetic effects and genetic aspects. Prog Biophys Mol Biol,2006;92(3);269-307.
Yan GX, WU Y, Liu T, et al. Phase 2 early after depolarization as a trigger of polymorphic ventricular tachycardia in acquired long-QT syndrome. Circulation, 2001; 103(23);2851-2856.
Shimizu W. Antzelevitch C. Differential effects of beta- adrenergicagonists and antagonists in LQT1, LQT2 and LQT3 models of the long QT syndrome. J Am Coll Cardiol,2000;35 (3):778-786.
Rada В, Lekstrom К, Damian S, et al. The pseudomonas toxin pyocyanin inhibits the dual oxidase-based antimicrobial system as it imposes oxidative stress on airway epithelial cells. J Immunol,2008; 181(7):4883-4893.
Harper RW. Xu С, Eiserich JP. et al. Differential regulation of dual NADPH oxidases/peroxidases, Duoxl and Duox2, by Thl and Th2 cytokines in respiratory tract epithelium. FEBS Lett,2005;579(21);491 1-4917.
Lambeth JD, Kawahara T, Diebold B. Regulation of Nox and Duox enzymatic activity and expression. Free Radic Biol Med. 2007;43(3):319-331.
Wu Y, Antony S, Juhasz A, et al. Up-regulation and sustained activation of Stall are essential for Interferon-у (IFN-y)-induced dual oxidase 2 (Duox2) and dual oxidase A2 (DuoxA2) expression in human pancreatic cancer cell lines. J Biol Chem.2011 ;286( 14): 12245-12256.
Schroder JM. Purification of antimicrobial peptides from human skin. Method Mol Biol,2010;618; 15-30.
Nomura I. Goleva E, Howell MD. et al. Cytokine milieu of atopic dermatitis, as compared to psoriasis, skin prevents induction of innate immune response genes. J Immunol, 2003; 171(6);3262-3269.
Geiszt M, Witta J, Baffi J, et al. Dual oxidases represent novel hydrogen peroxide sources supporting mucosal surface host defense. FASEB J ,2003; 17( 11); 1502-1504.
Harder J, Dressel S, Wittersheim M, et al. Enhanced expression and secretion of antimicrobial peptides in atopic dermatitis and after superficial skin injury. J Invest Dermatol, 2010;130(5):1355-1364.
Ballardini N, Johansson C, Lilja G, et al. Enhanced expression of the antimicrobial peptide LL-37 in lesional skin of adults with atopic eczema. Br J Dermatol,2009; 161 ( 1) :40-47.
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