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人乳头瘤病毒16型的E5癌蛋白可增强内皮素-1诱导的角质形成细胞生长。

The E5 oncoprotein of human papillomavirus type 16 enhances endothelin-1-induced keratinocyte growth.

作者信息

Venuti A, Salani D, Poggiali F, Manni V, Bagnato A

机构信息

Laboratory of Virology, Laboratory of Molecular Pathology and Ultrastructure, Regina Elena Institute for Cancer Research, CRS, via delle Messi d'Oro 156, Rome, 00158, Italy.

出版信息

Virology. 1998 Aug 15;248(1):1-5. doi: 10.1006/viro.1998.9227.

Abstract

Human keratinocytes express ETA receptors and produce endothelin-1 (ET-1), which stimulates growth response. Previously, we reported that a twofold increase in ETA receptors is present in human papillomavirus type 16 (HPV16) immortalized keratinocytes and that ET-1 induces enhanced proliferative response in these cell lines compared to normal cells. The present studies examine whether the E5 gene of HPV16 is responsible for the enhanced activity of ET-1 in HPV-transfected keratinocytes. The presence of the E5 gene in growth factor-starved keratinocytes induced the DNA synthesis and enhanced the mitogenic activity of ET-1 or epidermal growth factor. The selection of primary keratinocytes in growth factor-free medium with the addition of ET-1 as a growth factor showed that E5-transfected keratinocytes were able to grow and to form a higher number of larger colonies with respect to untransfected cells. This effect seems to be related to the interaction of E5 with the mitogenic signaling pathway of ET-1 rather than to an increase in the expression of the receptors for ET-1. In conclusion, our data demonstrate that E5 enhances ligand signaling in keratinocytes outside the EGF pathway by the amplification of the proliferative effect of ET-1/ETA receptor signaling.

摘要

人角质形成细胞表达内皮素A(ETA)受体并产生内皮素-1(ET-1),后者可刺激生长反应。此前,我们报道过人乳头瘤病毒16型(HPV16)永生化角质形成细胞中ETA受体增加了两倍,并且与正常细胞相比,ET-1在这些细胞系中诱导了增强的增殖反应。本研究检测HPV16的E5基因是否导致HPV转染的角质形成细胞中ET-1活性增强。在生长因子缺乏的角质形成细胞中存在E5基因可诱导DNA合成,并增强ET-1或表皮生长因子的促有丝分裂活性。在无生长因子培养基中加入ET-1作为生长因子来筛选原代角质形成细胞,结果显示,与未转染细胞相比 E5转染的角质形成细胞能够生长并形成更多更大的集落。这种效应似乎与E5和ET-1的促有丝分裂信号通路的相互作用有关,而不是与ET-1受体的表达增加有关。总之,我们的数据表明,E5通过放大ET-1/ETA受体信号的增殖效应,增强了表皮生长因子(EGF)通路以外角质形成细胞中的配体信号。

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