Suppr超能文献

16型和18型人乳头瘤病毒转染的人包皮角质形成细胞向永生化的转变:端粒酶激活及3p、10p、11q和/或18q处的等位基因缺失

Transition of human papillomavirus type 16 and 18 transfected human foreskin keratinocytes towards immortality: activation of telomerase and allele losses at 3p, 10p, 11q and/or 18q.

作者信息

Steenbergen R D, Walboomers J M, Meijer C J, van der Raaij-Helmer E M, Parker J N, Chow L T, Broker T R, Snijders P J

机构信息

Unit of Molecular Pathology, Department of Pathology, Free University Hospital, Amsterdam, The Netherlands.

出版信息

Oncogene. 1996 Sep 19;13(6):1249-57.

PMID:8808699
Abstract

This study aimed at resolving cellular genetic alterations in the process of in vitro immortalization of human keratinocytes by human papillomavirus (HPV) types 16 and 18. Four cell lines of primary human foreskin keratinocytes transfected with HPV 16 and HPV 18, respectively, were analysed during the transition from the mortal to immortal state. All cell lines showed strong telomerase activity at the immortal state, whereas no or only weak telomerase activity was detected in mortal precursor cells. This was consistent with telomere stabilization or restoration only observed in immortal cells. HPV physical state and copy number appeared constant during immortalization and HPV E6/E7 transcripts were present throughout. Immortalization was associated with clonal allele losses at 3p combined with either 11q or 18q or at 10p, dependent on the cell line. Moreover, a correlation was evident between the onset of telomerase activity and allele loss at 3p or 10p. All immortalized cells retained the capability to differentiate after growth in the presence of physiological calcium and serum. Moreover, one of the immortal cell lines displayed terminal differentiation after organotypic culturing on collagen rafts. The data suggest that (a) several pathways exist for HPV mediated immortalization that may involve genes residing at 3p, 10p, 11q and/or 18q; (b) 3p and 10p may encode genes involved in telomerase regulation; and (c) immortalization in vitro can be correlated with a spectrum of morphological changes varying from mild to severe dysplasia.

摘要

本研究旨在解析人乳头瘤病毒(HPV)16型和18型使人角质形成细胞体外永生化过程中的细胞遗传改变。在从有限增殖状态向永生化状态转变的过程中,分别对转染了HPV 16和HPV 18的四株原代人包皮角质形成细胞系进行了分析。所有细胞系在永生化状态时均表现出强烈的端粒酶活性,而在有限增殖的前体细胞中未检测到或仅检测到微弱的端粒酶活性。这与仅在永生化细胞中观察到的端粒稳定或恢复一致。HPV的物理状态和拷贝数在永生化过程中似乎保持不变,并且HPV E6/E7转录本始终存在。永生化与3p联合11q或18q或10p处的克隆性等位基因缺失相关,具体取决于细胞系。此外,端粒酶活性的出现与3p或10p处的等位基因缺失之间存在明显的相关性。所有永生化细胞在生理钙和血清存在的情况下生长后仍保留分化能力。此外,其中一株永生化细胞系在胶原筏上进行器官样培养后表现出终末分化。数据表明:(a)HPV介导的永生化存在多种途径,可能涉及位于3p、10p、11q和/或18q的基因;(b)3p和10p可能编码参与端粒酶调控的基因;(c)体外永生化可能与一系列从轻度到重度发育异常的形态学变化相关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验