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IL-1α and ATP mRNA expression after ultraviolet irradiation in human keratinocyte original-SCC 12F cells

机译:紫外线照射后人角质形成细胞原SCC 12F细胞中IL-1α和ATP mRNA表达

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Background Generally speaking, undifferentiated keratinocytes may synthesize a larger amount of IL-α and its production is decreased as cells complete differentiation gradually. Ultraviolet B (UVB) light can signigicantly stimulate the production and release of some cytokines. In this study we investigated the influence of UVB irradiation on IL-1α and adenosine triphosphoric (ATP) mRNA expressions in the human keratinocyte (KC) of original squamous cell carcinoma line (SCC 12F cells). Methods The cultured SCC 12F cells were irradiated with 30 mJ/cm~2 of UVB. Northern blot was employed to analyze the expression of IL-1α and ATP mRNA. Results There was a constitutive expression of IL-1α mRNA in SCC 12F cells. The expression increased in culturing time in regular KC medium and reached the highest expression at 120 hours. The expression level of IL-1α was up-regulated with two peaks at 6 hours and 72 hours, respectively after UVB irradiation. In comparison with IL-1α mRNA expression, ATP mRNA was down-regulated, with similar biphasic peaks, compared with the sham irradiated group. Conclusions SCC12F cells may express IL-1α mRNA constitutively. After UVB irradiation, the mRNA expression of IL-1α and ATP will show opposite effect because of inflammation/immunity and energy consumption mechanisms.
机译:背景技术一般而言,未分化的角质形成细胞可能合成大量的IL-α,并且随着细胞逐渐完全分化而降低其产量。紫外线B(UVB)可以显着刺激某些细胞因子的产生和释放。在这项研究中,我们研究了UVB辐射对原始鳞状细胞癌系(SCC 12F细胞)的人角质形成细胞(KC)中IL-1α和三磷酸腺苷(ATP)mRNA表达的影响。方法用30 mJ / cm〜2的UVB照射培养的SCC 12F细胞。用RNA印迹法分析IL-1α和ATP mRNA的表达。结果在SCC 12F细胞中IL-1αmRNA组成型表达。在常规KC培养基中培养时间表达增加,并在120小时达到最高表达。在UVB照射后,IL-1α的表达水平分别在6小时和72小时有两个峰值上调。与IL-1αmRNA表达相比,与假照射组相比,ATP mRNA被下调,具有相似的双相峰。结论SCC12F细胞可能组成性表达IL-1αmRNA。 UVB照射后,由于炎症/免疫和能量消耗机制,IL-1α和ATP的mRNA表达将显示相反的作用。

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