Alpha- and betapapillomavirus E6/E7 genes differentially modulate pro-inflammatory gene expression

被引:33
作者
De Andrea, Marco
Mondini, Michele
Azzimonti, Barbara
Dell'Oste, Valentina
Germano, Serena
Gaudino, Giovanni
Musso, Tiziana
Landolfo, Santo
Gariglio, Marisa
机构
[1] Med Sch Torino, Dept Publ Hlth & Microbiol, I-10126 Turin, Italy
[2] Med Sch Novara, Dept Clin & Expt Med, I-28100 Novara, Italy
[3] Univ Piemonte Orientale, DISCAFF & DFB Ctr, I-28100 Novara, Italy
关键词
cytokines; immune evasion; inflammation; nitric oxide; papillomavirus; skin diseases;
D O I
10.1016/j.virusres.2006.09.010
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Keratinocytes, the target cell of human papillomavirus (HPV) infection, can produce numerous cytokines and pro-inflammatory molecules which are important for the generation of an effective immune response. How this biological response, which involves the tumor stroma, is affected by the HPV oncoproteins within the epithelial cell itself is not clear. Here it is shown that oncoproteins of different HPV genotypes (alpha-versus beta-HPV genus) alter the expression of pro-inflammatory molecules in early passage primary human keratinocytes and the immortalized cell line HaCaT. HPV5 E6/E7 oncoproteins significantly induced interleukin-8 (IL-8), monocyte chemoattractant protein-1 (MCP-1) and intercellular adhesion molecule-1 (ICAM-1) expression. By contrast, the same molecules were down-regulated or not modulated in HPV16 E6/E7 transduced keratinocytes. Interestingly, HPV38 oncoproteins expression resulted in a lower induction of pro-inflammatory molecules, resembling the behavior displayed by the mucosal carcinogenic HPV 16. Finally, inducible nitric oxide synthase (iNOS) expression levels and nitric oxide (NO) production were induced at similar levels by all the HPV genotypes tested. These results further emphasize the different biological activities among HPV genotypes, and offer new insights into HPV-associated skin diseases. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:220 / 225
页数:6
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