[Latent Macrophage and Immature B Cell Lines Generated with Hygromycin-Resistant Murine Gammaherpesvirus 68 Genome Expresses Modest Levels of Viral miRNAs].

M Kara
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Abstract

Murine gammaherpesvirus 68 (MHV68) establishes latency mainly in B cells and causes lymphomas reminiscent of human gammaherpesvirus diseases in laboratory mice. To study the molecular mechanism of virus infection and how the viral determinants control cell and eventually cause tumorigenesis, readily available latently infected cell lines are essential. For in vitro MHV68 latency studies, only two cell culture systems have been available. Gammaherpesviruses are known to infect developing B cells and macrophages, therefore we aimed to expand the MHV68 latently infected cell line repertoire. Here, several latently infected immature B cell and macrophage-like cell line clones were generated. Hygromycin-resistant recombinant MHV68 was isolated from a laboratory-made latent cell line, HE2.1, and propagated to develop stable cell lines that carry the viral genome under hygromycin selection. Subclones of these cells lines were analyzed for viral miRNA expression by TaqMan qPCR and assessed for expression of a lytic viral transcript M3. The cell lines maintain the viral genome as an episome shown by the digestion-circularization PCR assay. Latently infected cell lines generated here do not express viral miRNAs higher than the parental cell line. However, these cell lines may provide an alternative tool to study latency mechanisms and miRNA target identification studies.

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[使用耐百日咳霉素的小鼠伽马疱疹病毒 68 基因组生成的潜伏巨噬细胞和未成熟 B 细胞系表达适度水平的病毒 miRNA】。]
小鼠γ疱疹病毒 68(MHV68)主要在 B 细胞中潜伏,并在实验室小鼠中引起与人类γ疱疹病毒疾病相似的淋巴瘤。要研究病毒感染的分子机制,以及病毒决定因子如何控制细胞并最终导致肿瘤发生,现成的潜伏感染细胞系至关重要。对于体外 MHV68 潜伏期研究,目前只有两种细胞培养系统可用。众所周知,γ疱疹病毒会感染发育中的 B 细胞和巨噬细胞,因此我们的目标是扩大 MHV68 潜伏感染细胞系的范围。在这里,我们生成了几种潜伏感染的未成熟 B 细胞和巨噬细胞样细胞系克隆。我们从实验室制造的潜伏细胞系 HE2.1 中分离出了耐百日咳霉素的重组 MHV68,并在百日咳霉素的选择下繁殖出携带病毒基因组的稳定细胞系。通过 TaqMan qPCR 分析了这些细胞系的亚克隆的病毒 miRNA 表达情况,并评估了溶解病毒转录本 M3 的表达情况。消化-环化 PCR 试验表明,这些细胞系以外显子的形式保持病毒基因组。这里生成的潜伏感染细胞系的病毒 miRNA 表达量并不比亲本细胞系高。不过,这些细胞系可为潜伏机制研究和 miRNA 靶点鉴定研究提供另一种工具。
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来源期刊
Molekulyarnaya Biologiya
Molekulyarnaya Biologiya Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
131
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