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人免疫缺陷病毒在单核细胞中复制的负调控。THP-1细胞中受限表达与潜伏表达的区别。

Negative regulation of human immune deficiency virus replication in monocytes. Distinctions between restricted and latent expression in THP-1 cells.

作者信息

Mikovits J A, Gonda M, Ruta M, Lohrey N C, Kung H F, Ruscetti F W

机构信息

Department of Biological Carcinogenesis Development Program, Program Resources, Inc., Frederick, Maryland.

出版信息

J Exp Med. 1990 May 1;171(5):1705-20. doi: 10.1084/jem.171.5.1705.

Abstract

In THP-1 monocytoid cells infected with HIV, viral expression can be regulated in several ways: (a) latency (no viral expression); (b) restricted expression (chronic low-level viral expression with little or no detectable virus released); and (c) continuous production. In cells with restricted HIV expression, nuclear factor(s) were found that blocked tat-associated DNA binding complex formation, suggesting that initiation of transcription was negatively regulated. Also, viral particles were seen budding into and accumulating within intracytoplasmic vacuoles with little virus released, suggesting multiple levels of regulation. These cells with restricted expression had no detectable viral antigens on the cell surface and were not lysed by IL-2-activated large granular lymphocytes. However, they could cause viral-mediated T cell cytolysis in cell-cell assays, suggesting viral transmission through cell contact. In addition, cells with latent HIV were identified and could still produce infectious virus after 5-azacytidine exposure 10 mo later. LPS and other treatments could increase viral production in cells with restricted but not latent expression, suggesting they occur by distinct mechanisms. These infected cells provide a reservoir for viral transmission to uninfected T cells that itself is not detected by immune surveillance mechanisms.

摘要

在感染了HIV的THP - 1单核细胞样细胞中,病毒表达可通过多种方式进行调节:(a) 潜伏状态(无病毒表达);(b) 受限表达(慢性低水平病毒表达,几乎没有或没有可检测到的病毒释放);以及(c) 持续产生。在HIV表达受限的细胞中,发现了一些核因子,它们阻止了与tat相关的DNA结合复合物的形成,这表明转录起始受到负调控。此外,可见病毒颗粒出芽进入胞质内空泡并在其中积累,很少有病毒释放,这表明存在多个调控水平。这些表达受限的细胞在细胞表面没有可检测到的病毒抗原,也不会被IL - 2激活的大颗粒淋巴细胞裂解。然而,在细胞 - 细胞试验中,它们可导致病毒介导的T细胞溶解,这表明病毒可通过细胞接触进行传播。此外,还鉴定出了具有潜伏性HIV的细胞,在10个月后暴露于5 - 氮杂胞苷后,它们仍能产生有传染性的病毒。脂多糖和其他处理可增加表达受限而非潜伏性表达的细胞中的病毒产生,这表明它们是通过不同的机制发生的。这些受感染的细胞为病毒传播到未感染的T细胞提供了一个储存库,而免疫监视机制本身无法检测到这个储存库。

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