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干扰素对人I型嗜T淋巴细胞病毒(HTLV-I)产生和释放的抑制作用。

Suppressive effects of interferons on the production and release of human T-lymphotropic virus type-I (HTLV-I).

作者信息

Oka T, Ohtsuki Y, Sonobe H, Furihata M, Miyoshi I

机构信息

Department of Pathology, Kochi Medical School, Japan.

出版信息

Arch Virol. 1990;115(1-2):63-73. doi: 10.1007/BF01310623.

Abstract

The effects of human alpha-, beta-, or gamma-interferon (IFN) on the replication and production of human T-lymphotrophic virus type-I (HTLV-I) were investigated in a human T-cell line, MT-2. Virus transmission and production estimated by syncytium formation and HTLV-I-associated reverse transcriptase (RT) activity were strongly suppressed in the presence of alpha- and beta-IFN, but not gamma-IFN. However, the expression of virus specific proteins gp46 but not p19, p24, p28, p36, and gp68 was affected with IFNs as revealed by Western blotting analysis. Electron microscopic observations showed that some of the HTLV-I particles were trapped in the intracellular vacuoles in the presence of high doses of alpha- or beta-IFN. Continuous supply of IFNs appeared to be essential for the constant suppression of RT activity. These results suggest that alpha- and beta-IFN do not inhibit HTLV-I gene expression strikingly but suppress processing or assembly of virus proteins and/or releasing of virions in the late phase of maturation.

摘要

在人T细胞系MT-2中研究了人α、β或γ干扰素(IFN)对人I型嗜T淋巴细胞病毒(HTLV-I)复制和产生的影响。通过合胞体形成和HTLV-I相关逆转录酶(RT)活性估计的病毒传播和产生在α-和β-IFN存在下受到强烈抑制,但γ-IFN不存在这种情况。然而,如蛋白质印迹分析所示,IFN影响病毒特异性蛋白gp46的表达,但不影响p19、p24、p28、p36和gp68的表达。电子显微镜观察表明,在高剂量α-或β-IFN存在下,一些HTLV-I颗粒被困在细胞内空泡中。持续供应IFN似乎是持续抑制RT活性所必需的。这些结果表明,α-和β-IFN不会显著抑制HTLV-I基因表达,但会在成熟后期抑制病毒蛋白的加工或组装和/或病毒粒子的释放。

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