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首页> 外文期刊>The Journal of investigative dermatology. >Interferon-gamma, a Strong Suppressor of Cell Proliferation, Induces Upregulation of Keratin K6, One of the Inflammatory- and Proliferation-Associated Keratins.
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Interferon-gamma, a Strong Suppressor of Cell Proliferation, Induces Upregulation of Keratin K6, One of the Inflammatory- and Proliferation-Associated Keratins.

机译:干扰素-γ,一种细胞增殖的强抑制剂,可诱导角蛋白K6的上调,角蛋白K6是与炎症和增殖相关的角蛋白之一。

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Keratin K6 is known as an inflammatory and hyperproliferative keratin, and is induced by an inflammatory and hyperproliferative agent. In this study, we demonstrated that interferon-gamma, an antiproliferative agent, also induces keratin K6. We used normal human ex vivo skin, normal human cultured keratinocytes, HaCaT keratinocytes, and DJM cells to examine the induction of K6 by interferon-gamma, by immunohistochemical staining, Western blot analysis, promoter chloramphenicol acetyl transferase assay, and reverse transcriptase polymerase chain reaction of mRNA. We succeeded in demonstrating the induction of keratin K6 by interferon-gamma in ex vivo human skin and HaCaT keratinocytes at the protein and message level, and in cultured normal human keratinocytes at the promoter level. The inhibition of the signal transducing activator of transcription 1 pathway by a dominant-negative transfer gene caused the inhibition of K6 induction by interferon-gamma, and the blocking of nuclear factor kappaB using antisense oligonucleotides also inhibited the K6 induction. We also blocked the released interleukin-1alpha from keratinocytes after stimulation with interferon-gamma by neutralizing antibodies, which showed a decrease in the K6 induction. Our results suggest that a small amount of interleukin-1alpha, which cannot induce K6 by itself, is secreted upon stimulation by interferon-gamma, and that the induction of K6 occurs through the synergistic effect of the interferon-gamma/signal transducing activator of transcription 1 and interleukin-1alphauclear factor kappaB pathways. This is the first report to describe K6 induction in epidermal keratinocytes by interferon-gamma and indicate a probable signal transduction pathway, and demonstrates that K6 is a possible partner of K17 in the inflammatory process.
机译:角蛋白K6被称为炎性和过度增殖性角蛋白,并且由炎性和过度增殖性剂诱导。在这项研究中,我们证明了抗干扰素-γ也能诱导角蛋白K6。我们使用正常人离体皮肤,正常人培养的角质形成细胞,HaCaT角质形成细胞和DJM细胞,通过免疫组化染色,Western印迹分析,启动子氯霉素乙酰转移酶测定和逆转录酶聚合酶链反应检测了干扰素-γ对K6的诱导。 mRNA。我们成功地证明了干扰素-γ在蛋白质和信息水平上在离体人类皮肤和HaCaT角质形成细胞中以及在启动子水平在培养的正常人角质形成细胞中对γ干扰素的诱导作用。显性负转移基因对转录1途径的信号转导激活因子的抑制导致干扰素-γ对K6诱导的抑制,并且使用反义寡核苷酸对核因子kappaB的阻断也抑制了K6诱导。我们还通过中和抗体阻断了干扰素-γ刺激后从角质形成细胞释放的白介素-1α的释放,这表明K6诱导的减少。我们的研究结果表明,干扰素-γ刺激后会分泌少量自身不能诱导K6的白介素-1α,并且K6的诱导是通过干扰素-γ/信号转导转录激活因子的协同作用而发生的。 1和白介素-1α/核因子κB途径。这是描述干扰素-γ在表皮角质形成细胞中诱导K6并表明可能的信号转导途径的第一份报告,并证明K6在炎症过程中可能是K17的伴侣。

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