4.6 Article

Neutrophil-dominant psoriasis-like skin inflammation induced by epidermal-specific expression of Raf in mice

Journal

JOURNAL OF DERMATOLOGICAL SCIENCE
Volume 58, Issue 1, Pages 28-35

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jdermsci.2010.01.004

Keywords

Raf; Skin inflammation; Neutrophil; Transgenic mice; Psoriasis

Categories

Funding

  1. JSPS KAKENHI [20591359, 21591476]
  2. High-Tech Research Center Grant
  3. Ministry of Health, Labour and Welfare, Health and Labour Sciences

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Background: Raf is one of the downstream effectors of Ras GTPases. The induction of Ref in the epidermis causes the proliferation of keratinocytes and epidermal hyperplasia. However, skin inflammation accompanying Ras-induced epidermal reactions has not been fully delineated. Objective: The aim of this study was to characterize inflammatory reactions induced by epidermal-specific Ref expression and to elucidate its role in skin inflammation. Methods: K14-Raf:ER transgenic mice, in which the 4-hydroxytamoxifen (4OHT)-responsive mutant estrogen receptor (ER) ligand binding domain-Rat fusion gene was expressed under control of the keratin 14 promoter, were used to characterize inflammatory reactions induced by Rat expression in the epidermis. Results: A single topical application of 4OHT induced the expression of phosphorylated extracellular signal-related kinase 1/2 and elicited neutrophil-dominant inflammatory infiltrates in the skin. The Ref expression also rapidly induced the production of several cytokines and chemokines, including VEGF and CXCL1, by keratinocytes and in mouse skin in vivo. Furthermore, CD4-positive cells from regional lymph nodes had the potential to differentiate into IFN-gamma- and IL17-producing cells. Treatment with an anti-Gr-1 antibody diminished the Rat-induced cutaneous inflammation and partially reversed the epidermal hyperplasia and hyperkeratosis. Conclusion: Activation of the Ref signaling pathway is involved in the epidermal hyperplasia and the neutrophil-dominant cutaneous inflammatory reactions which are characteristics of psoriasis. (C) 2010 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.

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