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人乳头瘤病毒16型E5蛋白影响上皮细胞系中的细胞间通讯。

Human papillomavirus type 16 E5 protein affects cell-cell communication in an epithelial cell line.

作者信息

Oelze I, Kartenbeck J, Crusius K, Alonso A

机构信息

Forschungsschwerpunkt Angewandte Tumorvirologie, Heidelberg, Federal Republic of Germany.

出版信息

J Virol. 1995 Jul;69(7):4489-94. doi: 10.1128/JVI.69.7.4489-4494.1995.

Abstract

The human papillomavirus type 16 (HPV16) E5 protein is considered to have weak oncogenic properties, and its function in infected human keratinocytes is unknown. HPV16 E5 protein has been found to localize to the Golgi apparatus and the plasma membrane. To analyze the effect of E5 on plasma membrane properties, cells from the human keratinocyte cell line HaCaT were transfected with the HPV16 E5 open reading frame under the control of an inducible promoter. The gap junction-mediated cell-cell communication of E5- and vector-transfected cells was analyzed by microinjection of Lucifer yellow to measure dye coupling of the cells. A strong impairment of dye transfer in E5-transfected cells but not in vector-transfected cells was observed, with more than 80% dye transfer inhibition 40 min after injection. This impairment correlated with dephosphorylation of connexin 43, the major gap junctional protein in HaCaT cells. Furthermore, the dye coupling inhibition was not the result of differentiation of the E5-expressing cells, since no overexpression of cytokeratin 1 or filaggrin, markers of HaCaT cell differentiation, could be observed. These results therefore strongly suggest a correlation between expression of the HPV16 E5 open reading frame, impairment of gap junction-mediated dye coupling, and dephosphorylation of connexin 43.

摘要

人乳头瘤病毒16型(HPV16)E5蛋白被认为具有较弱的致癌特性,其在感染的人角质形成细胞中的功能尚不清楚。已发现HPV16 E5蛋白定位于高尔基体和质膜。为了分析E5对质膜特性的影响,在可诱导启动子的控制下,用人角质形成细胞系HaCaT的细胞转染HPV16 E5开放阅读框。通过显微注射荧光素黄来分析E5转染细胞和载体转染细胞的间隙连接介导的细胞间通讯,以测量细胞的染料偶联。观察到E5转染细胞中染料转移受到强烈损害,而载体转染细胞中未观察到这种情况,注射后40分钟染料转移抑制率超过80%。这种损害与连接蛋白43(HaCaT细胞中的主要间隙连接蛋白)的去磷酸化相关。此外,染料偶联抑制不是表达E5的细胞分化的结果,因为未观察到HaCaT细胞分化标志物细胞角蛋白1或丝聚蛋白的过表达。因此,这些结果强烈表明HPV16 E5开放阅读框的表达、间隙连接介导的染料偶联受损与连接蛋白43的去磷酸化之间存在相关性。

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