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人乳头瘤病毒(HPV)16 型癌蛋白对人角质形成细胞中内披蛋白表达的影响。

Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes.

机构信息

Department of Medical Microbiology, Medical and Health Science Centre, University of Debrecen, 4032 Debrecen, Nagyerdei krt, 98, Hungary.

出版信息

Virol J. 2012 Feb 14;9:36. doi: 10.1186/1743-422X-9-36.

Abstract

BACKGROUND

The human papillomavirus (HPV) life cycle is closely linked to keratinocyte differentiation. Oncogenic HPV infection has been shown to hamper the normal differentiation of keratinocytes; however, the underlying mechanisms responsible for this phenomenon are yet to be clarified. Here, we aimed to study the effects of HPV16 E6 and E7 oncogenes on the expression of involucrin (IVL), an established marker of keratinocyte differentiation, in human foreskin keratinocyte (HFK) cells.

RESULTS

The differentiation of HFK cells by serum and high calcium significantly increased both the mRNA and the protein levels of IVL. The E6 and E7 oncoproteins of HPV16 together caused strong down-regulation of IVL mRNA and protein both in proliferating and in differentiating HFK cells. To study the effects of HPV oncogenes on the IVL promoter, we made transient transfection assays and luciferase tests and found that HPV 16 E6 but not E7 repressed IVL promoter activity in proliferating HFK cells. The inhibitory effect of HPV 16 E6 on the human IVL promoter could be localised to the proximal regulatory region (PRR) of the gene.

CONCLUSIONS

These results suggest that the down-regulation of IVL promoter activity by HPV 16 E6 significantly contribute to the inhibition of endogenous IVL expression by the HPV 16 oncoproteins. In contrast, the down-regulation of endogenous IVL expression by HPV16 E7 is probably not caused by a direct and specific effect of E7 on the IVL promoter.

摘要

背景

人乳头瘤病毒(HPV)的生命周期与角质形成细胞分化密切相关。致癌 HPV 感染已被证明会阻碍角质形成细胞的正常分化;然而,导致这种现象的潜在机制尚不清楚。在这里,我们旨在研究 HPV16 E6 和 E7 癌基因对人包皮角质形成细胞(HFK)中内披蛋白(IVL)表达的影响,IVL 是角质形成细胞分化的一个既定标志物。

结果

血清和高钙诱导的 HFK 细胞分化显著增加了 IVL 的 mRNA 和蛋白水平。HPV16 的 E6 和 E7 癌蛋白共同导致增殖和分化的 HFK 细胞中 IVL mRNA 和蛋白的强烈下调。为了研究 HPV 癌基因对 IVL 启动子的影响,我们进行了瞬时转染测定和荧光素酶试验,发现 HPV16E6 而非 E7 抑制了增殖 HFK 细胞中 IVL 启动子的活性。HPV16E6 对人 IVL 启动子的抑制作用可以定位于基因的近端调控区(PRR)。

结论

这些结果表明,HPV16E6 对 IVL 启动子活性的下调显著导致 HPV16 癌蛋白对内源性 IVL 表达的抑制。相比之下,HPV16E7 对内源性 IVL 表达的下调可能不是由 E7 对 IVL 启动子的直接和特异作用引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e73d/3296608/94758d40b63c/1743-422X-9-36-1.jpg

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