Literature DB >> 18040150

[Subcellular locations at which HIV-1 assembles].

Akira Ono1.   

Abstract

Virus particle formation of HIV-1 is driven by the viral structural protein Gag. In most cell types including T cells, Gag assembles into virus particles at the plasma membrane whereas, in HIV-1-infected macrophages, Gag and virus particles have been shown to accumulate in intracellular vesicles. At the moment, what causes this difference between cell types remains unknown. However, recent findings on the relationships between Gag and the cellular membrane system have substantially increased our understanding of the mechanisms by which sites of virus assembly are determined. I will review our current knowledge regarding the roles played by endosomal trafficking pathways, membrane microdomains, and plasma membrane lipids, and discuss the physiological significance of the interactions between Gag and specific membrane structures.

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Year:  2007        PMID: 18040150     DOI: 10.2222/jsv.57.9

Source DB:  PubMed          Journal:  Uirusu        ISSN: 0042-6857


  2 in total

1.  Efficient production of HIV-1 virus-like particles from a mammalian expression vector requires the N-terminal capsid domain.

Authors:  Pascal Jalaguier; Karine Turcotte; Alexis Danylo; Réjean Cantin; Michel J Tremblay
Journal:  PLoS One       Date:  2011-11-30       Impact factor: 3.240

2.  Opposing regulation of endolysosomal pathways by long-acting nanoformulated antiretroviral therapy and HIV-1 in human macrophages.

Authors:  Mariluz Araínga; Dongwei Guo; Jayme Wiederin; Pawel Ciborowski; JoEllyn McMillan; Howard E Gendelman
Journal:  Retrovirology       Date:  2015-01-22       Impact factor: 4.602

  2 in total

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