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缺乏潜伏膜蛋白2的爱泼斯坦-巴尔病毒使B细胞永生化,其效率与野生型病毒无法区分。

Epstein-Barr virus lacking latent membrane protein 2 immortalizes B cells with efficiency indistinguishable from that of wild-type virus.

作者信息

Speck Peter, Kline Kimberly A, Cheresh Paul, Longnecker Richard

机构信息

Department of Microbiology-Immunology, Northwestern University Medical School, Room 6-231 Ward Building, 303 East Chicago Avenue, Chicago, Illinois 60611, USA1.

出版信息

J Gen Virol. 1999 Aug;80 ( Pt 8):2193-2203. doi: 10.1099/0022-1317-80-8-2193.

Abstract

Epstein-Barr virus (EBV) is a human herpesvirus that efficiently transforms and immortalizes human primary B lymphocytes. In this study, the role of latent membrane protein 2 (LMP2) in EBV growth transformation was investigated. LMP2 is a virally encoded membrane protein expressed in EBV-immortalized B cells previously shown to be nonessential for EBV transformation. However, a recent study reported that LMP2 may be an important determinant for efficient B cell transformation (Brielmeier et al., Journal of General Virology 77, 2807-2818, 1996). In this study a deletion mutation was introduced into the LMP2 gene using an E. coli mini-EBV construct containing sufficient EBV DNA to result in growth transformation of primary B cells. In an alternative approach, the introduction of the gene encoding the enhanced green fluorescent protein (EGFP) by homologous recombination into the LMP2 gene of EBV strain B95-8, generating the same LMP2 deletion mutation is reported. Careful quantification of B cell transformation using the EGFP+ LMP2- recombinant virus determined that in liquid culture medium or in culture medium containing soft agarose there was no difference in the ability of LMP2- virus to immortalize primary human B cells when compared to that of wild-type virus.

摘要

爱泼斯坦-巴尔病毒(EBV)是一种人类疱疹病毒,可有效转化人类原代B淋巴细胞并使其永生化。在本研究中,对潜伏膜蛋白2(LMP2)在EBV生长转化中的作用进行了研究。LMP2是一种病毒编码的膜蛋白,在EBV永生化的B细胞中表达,此前已证明其对EBV转化并非必需。然而,最近的一项研究报告称,LMP2可能是有效B细胞转化的重要决定因素(Brielmeier等人,《普通病毒学杂志》77,2807 - 2818,1996)。在本研究中,使用含有足够EBV DNA以导致原代B细胞生长转化的大肠杆菌微型EBV构建体,将缺失突变引入LMP2基因。在另一种方法中,通过同源重组将编码增强型绿色荧光蛋白(EGFP)的基因引入EBV菌株B95 - 8的LMP2基因中,据报道产生了相同的LMP2缺失突变。使用EGFP + LMP2 - 重组病毒对B细胞转化进行仔细定量分析,结果表明,在液体培养基或含有软琼脂糖的培养基中,与野生型病毒相比,LMP2 - 病毒使原代人类B细胞永生化的能力没有差异。

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