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HIV-1 限制因子的小鼠基因敲除模型。

Mouse knockout models for HIV-1 restriction factors.

机构信息

Medical Research Council Human Immunology Unit, Medical Research Council Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, Headley Way, University of Oxford, Oxford, OX3 9DS, UK,

出版信息

Cell Mol Life Sci. 2014 Oct;71(19):3749-66. doi: 10.1007/s00018-014-1646-8. Epub 2014 May 23.

Abstract

Infection of cells with human immunodeficiency virus 1 (HIV-1) is controlled by restriction factors, host proteins that counteract a variety of steps in the life cycle of this lentivirus. These include SAMHD1, APOBEC3G and tetherin, which block reverse transcription, hypermutate viral DNA and prevent progeny virus release, respectively. These and other HIV-1 restriction factors are conserved and have clear orthologues in the mouse. This review summarises studies in knockout mice lacking HIV-1 restriction factors. In vivo experiments in such animals have not only validated in vitro data obtained from cultured cells, but have also revealed new findings about the biology of these proteins. Indeed, genetic ablation of HIV-1 restriction factors in the mouse has provided evidence that restriction factors control retroviruses and other viruses in vivo and has led to new insights into the mechanisms by which these proteins counteract infection. For example, in vivo experiments in knockout mice demonstrate that virus control exerted by restriction factors can shape adaptive immune responses. Moreover, the availability of animals lacking restriction factors opens the possibility to study the function of these proteins in other contexts such as autoimmunity and cancer. Further in vivo studies of more recently identified HIV-1 restriction factors in gene targeted mice are, therefore, justified.

摘要

细胞感染人类免疫缺陷病毒 1(HIV-1)受到限制因子的控制,这些宿主蛋白可以抵抗这种慢病毒生命周期中的多种步骤。这些因子包括 SAMHD1、APOBEC3G 和 tetherin,它们分别阻断逆转录、使病毒 DNA 产生大量突变以及阻止子代病毒释放。这些因子和其他 HIV-1 限制因子在小鼠中是保守的,并且具有明确的直系同源物。本文综述了缺乏 HIV-1 限制因子的基因敲除小鼠的研究。在这些动物的体内实验不仅验证了从培养细胞中获得的体外数据,还揭示了这些蛋白生物学的新发现。事实上,在小鼠中遗传剔除 HIV-1 限制因子提供了限制因子在体内控制逆转录病毒和其他病毒的证据,并深入了解了这些蛋白抵抗感染的机制。例如,在基因敲除小鼠的体内实验中证明,限制因子对病毒的控制可以影响适应性免疫反应。此外,缺乏限制因子的动物的可用性为研究这些蛋白在自身免疫和癌症等其他情况下的功能提供了可能性。因此,有理由在基因靶向小鼠中进一步研究最近发现的 HIV-1 限制因子的体内功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5853/11113334/8ac44a3a8ed0/18_2014_1646_Fig1_HTML.jpg

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