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• W2105280985 abstract "Atopic dermatitis (AD) is a common allergic disease, imposing large social and economic burdens worldwide. Atopic dermatitis is characterized by eczematous skin lesions and immunoglobulin E (IgE) hypersecretion. We investigated the role of JNK1 on the development of AD in mice. The vitamin D3 analogue MC903, a psoriasis therapeutic drug, was used to induce AD-like symptoms in wild-type (WT) and JNK1−/− mice. The symptoms of AD were less severe in JNK1−/− mice compared with WT mice. JNK1−/− mice showed less ear thickening and infiltration of eosinophils and mast cells in AD-like lesions than did WT mice when treated with MC903. MC903-treated JNK1−/− mice also showed significantly lower level of serum IgE, which was elevated in MC903-treated WT mice. Splenocytes isolated from MC903-treated WT and JNK1−/− mice were stimulated with anti-CD3 and anti-CD28 monoclonal antibodies. Splenocytes from JNK1−/− mice produced lower levels of T-helper (Th2) cytokines (interleukin-4 and -13) and transcription factor GATA-binding protein 3, and produced increased levels of the Th1 cytokines interferon-γ and transcription factor T-box expressed in T cells. Our results indicate that JNK1 plays an important role in the pathogenesis of AD and may be a useful target for therapies to ameliorate AD." @default.
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• W2105280985 date "2013-09-17" @default.
• W2105280985 modified "2023-10-10" @default.
• W2105280985 title "The Atopic Dermatitis-Like Symptoms Induced by MC903 Were Alleviated in JNK1 Knockout Mice" @default.
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• W2105280985 doi "https://doi.org/10.1093/toxsci/kft215" @default.
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