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首页> 外文期刊>Journal of Investigative Dermatology Symposium Proceedings >Regulation of Skin Pigmentation and Thickness by Dickkopf 1 (DKK1)
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Regulation of Skin Pigmentation and Thickness by Dickkopf 1 (DKK1)

机译:Dickkopf 1(DKK1)对皮肤色素沉着和厚度的调节

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Dickkopf 1 (DKK1), an inhibitor of Wnt signaling, not only functions as a head inducer during development, but also regulates joint remodeling and bone formation, which suggests roles for DKK1 in the pathogenesis of rheumatoid arthritis and multiple myeloma. We recently demonstrated that levels of DKK1 in palmoplantar dermal fibroblasts are physiologically higher than those observed in non-palmoplantar dermal fibroblasts. Thus, the DKK1-rich mesenchyme in palmoplantar dermis affects the overlying epithelium and induces a palmoplantar phenotype in the epidermis. More specifically, DKK1 suppresses melanocyte function and growth through the regulation of microphthalmia-associated transcription factor (MITF) and -catenin. Furthermore, DKK1 induces the expression of keratin 9 and -Kelch-like ECT2-interacting protein (KLEIP) but downregulates the expression of -catenin, glycogen synthase kinase 3, protein kinase C, and proteinase-activated receptor-2 (PAR-2) in keratinocytes. Treatment of reconstructed skin with DKK1 reproduces the hypopigmentation and thickening of skin through Wnt/-catenin signaling. These studies elucidate why human palmoplantar skin is thicker and paler than non-palmoplantar skin through the secretion of DKK1 by fibroblasts that affect the overlying epidermis. Thus, DKK1 may be useful for reducing skin pigmentation and for thickening photo-aged skin and palmoplantar wounds caused by diabetes mellitus and rheumatic skin diseases.Abbreviations: DKK1, dickkopf 1; MITF, microphthalmia-associated transcription factor; PAR-2, proteinase-activated receptor-2; KLEIP, -Kelch-like ECT2-interacting protein
机译:Dntkopf 1(DKK1)是Wnt信号的抑制剂,不仅在发育过程中起头诱导剂的作用,而且还调节关节重塑和骨形成,这提示DKK1在类风湿性关节炎和多发性骨髓瘤的发病机理中的作用。我们最近证明,掌plant皮肤成纤维细胞中DKK1的水平比非掌plant皮肤成纤维细胞中的生理水平高。因此,掌plant真皮中富含DKK1的间充质会影响上皮并诱导表皮中的掌plant表型。更具体地说,DKK1通过调节小眼科相关转录因子(MITF)和-catenin抑制黑素细胞功能和生长。此外,DKK1诱导角蛋白9和-Kelch样ECT2相互作用蛋白(KLEIP)的表达,但下调-catenin,糖原合酶激酶3,蛋白激酶C和蛋白酶激活受体2(PAR-2)的表达。在角质形成细胞中。用DKK1处理重建的皮肤可通过Wnt / -catenin信号转导色素沉着不足和皮肤增厚。这些研究阐明了为什么人的掌plant皮肤通过影响上表皮的成纤维细胞分泌DKK1而比非掌plant皮肤更厚更白。因此,DKK1可用于减少皮肤色素沉着和用于增厚由糖尿病和风湿性皮肤病引起的光老化的皮肤和掌plant伤口。 MITF,与小眼症相关的转录因子; PAR-2,蛋白酶激活受体2; KLEIP,-Kelch样ECT2相互作用蛋白

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