首页> 外文期刊>European Journal of Cell Biology: Journal of Deutsche Gesellschaft fur Elektronenmikroskopie: Journal of Deutsche Gesellschaft fur Zellbiologie >Human Kruppel-like factor5/KLF5: Synergy with NF-kappa B/Rel factors and expression in human skin and hair follicles
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Human Kruppel-like factor5/KLF5: Synergy with NF-kappa B/Rel factors and expression in human skin and hair follicles

机译:人Kruppel样factor5 / KLF5:与NF-κB/ Rel因子的协同作用以及在人皮肤和毛囊中的表达

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摘要

In this report we describe the identification of Kruppel-like factor 5 (KLF5/BTEB2) in a yeast one-hybrid screen using a keratinocyte-specific, NF-kappaB binding site as bait. The KLF5 cDNA encodes a larger protein of 457 aa rather than the earlier reported protein of 209 aa. The full-length KLF5 functions as a transactivator in HepG2 cells, and the stimulation of cells with 12-O-tetradecanoylphorbol-13-acetate (TPA) can modulate its transcriptional activity. Overexpression of KLF5 leads to an increase in the TPA response from VLTRE, a TPA-inducible enhancer element that shows keratinocyte specificity with respect to Rel/NF-kappaB binding. The KLF5-mediated transcriptional increase is not observed in the presence of overexpressed NF-kappaB inhibitor, IkappaBalpha. Cotransfection of KLF5 and the p65 subunit of NF-kappaB, results in a synergistic transactivation of the VLTRE-luciferase reporter. The KLF5 mRNA and the protein is expressed in keratinocytes and throughout the adult human epidermis. Its expression is especially strong in the matrix and the inner root sheath cuticle layer of the hair follicle, sebaceous glands and sweat glands. Considering the TPA-responsiveness and expression pattern, we propose that KLF5 like another member of its family KLF4/GKLF may play an important role in skin morphogenesis and carcinogenesis potentially via its interaction with NF-kappaB factors.
机译:在本报告中,我们描述了使用角质形成细胞特异性NF-κB结合位点作为诱饵的酵母一杂交筛选中Kruppel样因子5(KLF5 / BTEB2)的鉴定。 KLF5 cDNA编码的更大蛋白质为457aa,而不是先前报道的209aa的蛋白质。全长KLF5在HepG2细胞中起反式激活剂的作用,用12-O-十四烷酰佛波醇13-乙酸盐(TPA)刺激细胞可以调节其转录活性。 KLF5的过表达导致来自VLTRE的TPA反应增加,VLTRE是TPA诱导型增强子,相对于Rel / NF-kappaB结合显示出角质形成细胞特异性。在过表达的NF-κB抑制剂IkappaBalpha的存在下,未观察到KLF5介导的转录增加。 KLF5和NF-κB的p65亚基的共转染导致VLTRE-荧光素酶报道分子的协同反式激活。 KLF5 mRNA和蛋白质在角质形成细胞和整个成年人类表皮中表达。它的表达在毛囊,皮脂腺和汗腺的基质和内根鞘表皮层特别强。考虑到TPA反应性和表达模式,我们建议KLF5像其家族KLF4 / GKLF的另一个成员一样,可能通过与NF-κB因子相互作用而在皮肤形态发生和癌变中起重要作用。

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