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http://dx.doi.org/10.5483/BMBRep.2012.45.6.036

Suppression of 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced skin inflammation in mice by transduced Tat-Annexin protein  

Lee, Sun-Hwa (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Kim, Dae-Won (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Eom, Seon-Ae (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Jun, Se-Young (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Park, Mee-Young (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Kim, Duk-Soo (Department of Anatomy, College of Medicine, Soonchunhyang University)
Kwon, Hyung-Joo (Department of Microbiology, College of Medicine, Hallym University)
Kwon, Hyeok-Yil (Department of Physiology, College of Medicine, Hallym University)
Han, Kyu-Hyung (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Park, Jin-Seu (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Hwang, Hyun-Sook (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Eum, Won-Sik (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Choi, Soo-Young (Department of Biomedical Science and Research Institute of Bioscience and Biotechnology, Hallym University)
Publication Information
BMB Reports / v.45, no.6, 2012 , pp. 354-359 More about this Journal
Abstract
We examined that the protective effects of ANX1 on 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced skin inflammation in animal models using a Tat-ANX1 protein. Topical application of the Tat-ANX1 protein markedly inhibited TPA-induced ear edema and expression levels of cyclooxygenase-2 (COX-2) as well as pro-inflammatory cytokines such as interleukin-1 beta (IL-$1{\beta}$), IL-6, and tumor necrosis factor-alpha (TNF-${\alpha}$). Also, application of Tat-ANX1 protein significantly inhibited nuclear translocation of nuclear factor-kappa B (NF-${\kappa}B$) and phosphorylation of p38 and extracellular signal-regulated kinase (ERK) mitogen-activated protein kinase (MAPK) in TPA-treated mice ears. The results indicate that Tat-ANX1 protein inhibits the inflammatory response by blocking NF-${\kappa}B$ and MAPK activation in TPA-induced mice ears. Therefore, the Tat-ANX1 protein may be useful as a therapeutic agent against inflammatory skin diseases.
Keywords
Cytokine; Inflammation; MAPK; Tat-ANX1; TPA;
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Times Cited By Web Of Science : 2  (Related Records In Web of Science)
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