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半胱胺能有效抑制急性和慢性感染的人类细胞中的体外HIV复制。

Cystamine potently suppresses in vitro HIV replication in acutely and chronically infected human cells.

作者信息

Bergamini A, Capozzi M, Ghibelli L, Dini L, Salanitro A, Milanese G, Wagner T, Beninati S, Pesce C D, Amici C

机构信息

Department of Public Health, University of Rome Tor Vergata, Italy.

出版信息

J Clin Invest. 1994 May;93(5):2251-7. doi: 10.1172/JCI117223.

Abstract

We have investigated the effects of cystamine on the replication of human immunodeficiency virus (HIV) in human lymphocytes and macrophages, the natural targets of HIV in vivo. Treatment of chronically infected macrophages with cystamine, at a concentration (500 microM) that did not show any cytotoxic or cytostatic effects, strongly decreased (> 80%) HIV-p24 antigen production and completely abolished the production of infectious viral particles. Cystamine does not affect viral transcription, translation or protein processing; indeed, all HIV proteins are present in a pattern similar to that of nontreated cells. Instead, cystamine interferes with the orderly assembly of HIV virions, as shown by electron microscopy analysis, that reveals only defective viral particles in treated cells. Moreover, suppression of HIV replication, due to the inhibition of proviral DNA formation was observed in acutely infected lymphocytes and macrophages pretreated with cystamine. These results show that cystamine potently suppresses HIV replication in human cells by contemporaneously blocking at least two independent steps of the viral life cycle, without affecting cell viability, suggesting that this compound may represent a new possibility towards the treatment of HIV-1 infection.

摘要

我们已经研究了半胱胺对人类免疫缺陷病毒(HIV)在人类淋巴细胞和巨噬细胞(HIV在体内的天然靶细胞)中复制的影响。用半胱胺处理慢性感染的巨噬细胞,其浓度(500微摩尔)未显示出任何细胞毒性或细胞抑制作用,能强烈降低(>80%)HIV-p24抗原的产生,并完全消除感染性病毒颗粒的产生。半胱胺不影响病毒转录、翻译或蛋白质加工;实际上,所有HIV蛋白的存在模式与未处理细胞相似。相反,如电子显微镜分析所示,半胱胺会干扰HIV病毒体的有序组装,该分析显示处理过的细胞中只有缺陷病毒颗粒。此外,在用半胱胺预处理的急性感染淋巴细胞和巨噬细胞中,观察到由于前病毒DNA形成受到抑制而导致的HIV复制受到抑制。这些结果表明,半胱胺通过同时阻断病毒生命周期中至少两个独立步骤,有力地抑制了人类细胞中的HIV复制,而不影响细胞活力,这表明该化合物可能为治疗HIV-1感染提供了一种新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bb/294379/1eca9f3b2e37/jcinvest00034-0389-a.jpg

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