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[原单核细胞系U937衍生亚克隆对HIV-1感染及凋亡诱导的易感性研究]

[Studies on susceptibility of promonocytic cell line U937-derived subclones to HIV-1 infection and apoptosis induction].

作者信息

Kameoka M

机构信息

Section of Serology, Hokkaido University, Sapporo, Japan.

出版信息

Hokkaido Igaku Zasshi. 1996 Jul;71(4):489-508.

PMID:8809573
Abstract

The promonocytic cell line U937, when infected with lymphotropic human immunodeficiency virus type 1 (HIV-1), becomes a continuous virus producer. A total of 46 subclones was isolated by limiting dilution of U937. These subclones were classified into three (2 high, 42 middle, and 2 low) types based on their susceptibility to HIV-1 infection, i.e., the appearance of viral antigens and following virus production. Analyses of cell surface antigens on representative 2 subclones in each type revealed that CD4 expression is similar level in all subclones, while LFA-1 expression is significantly lower than middle- and low-type subclones. After infection of HIV-1, different characteristics were observed among three types of subclones. First, superoxide was generated in the high-type subclones during all infection stages, even before HIV-1 replication, while in middle- and low-type subclones only transiently at acute phase of HIV-1 replication. Second, the cell differentiation was induced by HIV-1 infection only in high-type subclones, but not in low-type subclones. Thus, these results suggest that these subclones are different in the differentiation stage of the cell type. Analysis of the HIV-1 life cycles such as adsorption, reverse transcription, integration, transcription, and translation in the subclones, revealed that the different susceptibility is associated with the accumulation of unintegrated extra-chromosomal forms of HIV-1 DNA. In addition, the low-, but not high-type, subclones were sensitive for the apoptosis by treatment with TNF-alpha, anti-Fas antibody, or defective non-infectious HIV-1 particles. Thus, U937 could be devided into at least two populations, i.e., one for HIV-1 productive infection and the other for apoptosis without new HIV-1 replication, similarly as in the situation in infected HIV-1 carriers.

摘要

原单核细胞系U937感染亲淋巴细胞性1型人类免疫缺陷病毒(HIV-1)后,会成为持续的病毒产生细胞。通过对U937进行有限稀释,共分离出46个亚克隆。根据它们对HIV-1感染的易感性,即病毒抗原的出现及随后的病毒产生情况,将这些亚克隆分为三种类型(2个高型、42个中型和2个低型)。对每种类型中代表性的2个亚克隆的细胞表面抗原进行分析发现,所有亚克隆中CD4的表达水平相似,而淋巴细胞功能相关抗原-1(LFA-1)的表达明显低于中型和低型亚克隆。HIV-1感染后,三种类型的亚克隆呈现出不同的特征。首先,高型亚克隆在所有感染阶段都会产生超氧化物,甚至在HIV-1复制之前,而中型和低型亚克隆仅在HIV-1复制急性期短暂产生超氧化物。其次,HIV-1感染仅在高型亚克隆中诱导细胞分化,低型亚克隆中则未诱导。因此,这些结果表明这些亚克隆在细胞类型的分化阶段存在差异。对亚克隆中HIV-1生命周期(如吸附、逆转录、整合、转录和翻译)的分析表明,不同的易感性与未整合的HIV-1 DNA染色体外形式的积累有关。此外,低型亚克隆(而非高型亚克隆)对肿瘤坏死因子-α(TNF-α)、抗Fas抗体或缺陷性非感染性HIV-1颗粒处理诱导的凋亡敏感。因此,U937可至少分为两个群体,一个群体用于HIV-1的有效感染,另一个群体用于在无新HIV-1复制情况下的凋亡,这与HIV-1感染携带者的情况类似。

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