HPV16 E7 通过 AP2 复合物调节细胞表面 MET 和 CD109 的表达。

IF 4.7 Q1 VIROLOGY
Oscar Trejo-Cerro , Om Basukala , Michael P. Myers , Lawrence Banks
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引用次数: 0

摘要

多种细胞通路会受到 HPV E6 和 E7 肿瘤蛋白的影响,包括内吞和细胞转运。HPV-16 E7 可靶向适配蛋白(AP)复合物,该复合物包含内吞转运过程中的重要蛋白质。为了进一步研究 HPV E7 在这一过程中的作用,我们分析了表达 HPV-16 E7 的 NIKS 细胞中细胞表面蛋白的表达情况。我们发现,HPV-16 E7 通过与 AP2 相互作用调控不同的细胞表面蛋白。我们观察到,在表达 E7 的细胞中,MET 和 CD109 膜蛋白的表达似乎被上调。此外,HPV-16 E7 破坏了 MET 和 CD109 与 AP2 蛋白的相互作用。此外,在没有 HPV-16 E7 的情况下,HPV 阳性细胞系中 MET 和 CD109 的细胞膜表达下调。这些结果拓展了我们对 E7 功能的认识,并开辟了受这种肿瘤蛋白影响的新的潜在细胞通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HPV16 E7 modulates the cell surface expression of MET and CD109 via the AP2 complex

Multiple cellular pathways are affected by HPV E6 and E7 oncoproteins, including endocytic and cellular trafficking. HPV-16 E7 can target the adaptor protein (AP) complex, which contains proteins important during endocytosis transport. To further investigate the role of HPV E7 during this process, we analysed the expression of cell surface proteins in NIKS cells expressing HPV-16 E7. We show that different cell surface proteins are regulated by HPV-16 E7 via interaction with AP2. We observed that the expression of MET and CD109 membrane protein seems to be upregulated in cells expressing E7. Moreover, the interaction of MET and CD109 with AP2 proteins is disrupted by HPV-16 E7. In addition, in the absence of HPV-16 E7, there is a downregulation of the cell membrane expression of MET and CD109 in HPV-positive cell lines. These results expand our knowledge of the functions of E7 and open new potential cellular pathways affected by this oncoprotein.

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来源期刊
Tumour Virus Research
Tumour Virus Research Medicine-Infectious Diseases
CiteScore
6.50
自引率
2.30%
发文量
16
审稿时长
56 days
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