Annexin 2:: A novel human immunodeficiency virus type 1 Gag binding protein involved in replication in monocyte-derived macrophages

被引:85
作者
Ryzhova, EV
Vos, RM
Albright, AV
Harrist, AV
Harvey, T
González-Scarano, F
机构
[1] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
D O I
10.1128/JVI.80.6.2694-2704.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human immunodeficiency virus (HIV) replication in the major natural target cells, CD4(+) T lymphocytes and macrophages, is parallel in many aspects of the virus life cycle. However, it differs as to viral assembly and budding, which take place on plasma membranes in T cells and on endosomal membranes in macrophages. It has been postulated that cell type-specific host factors may aid in directing viral assembly to distinct destinations. In this study we defined annexin 2 (Anx2) as a novel HIV Gag binding partner in macrophages. Anx2-Gag binding-was confined to productively infected macrophages and was not detected in quiescently infected monocyte-derived macrophages (MDM) in which an HIV replication block was mapped to the late stages of the viral life cycle (A. V. Albright, R. M. Vos, and F. Gonzalez-Scarano, Virology 325:328-339, 2004). We demonstrate that the Anx2-Gag interaction likely occurs at the limiting membranes of late endosomes/multivesicular bodies and that Anx2 depletion is associated with a significant decline in the infectivity of released virions; this coincided with incomplete Gag processing and inefficient incorporation of CD63. Cumulatively, our data suggest that Anx2 is essential for the proper assembly of HIV in MDM.
引用
收藏
页码:2694 / 2704
页数:11
相关论文
共 49 条
[1]   Selected amino acid substitutions in the C-terminal region of human immunodeficiency virus type 1 capsid protein affect virus assembly and release [J].
Abdurahman, S ;
Höglund, S ;
Goobar-Larsson, L ;
Vahlne, A .
JOURNAL OF GENERAL VIROLOGY, 2004, 85 :2903-2913
[2]   A successful pregnancy following SEM fine tuning of hormonal priming [J].
Adams S.M. ;
Murphy C.R. .
BMC Pregnancy and Childbirth, 1 (1)
[3]   Low-level HIV replication in mixed glial cultures is associated with alterations in the processing of p55Gag [J].
Albright, AV ;
Vos, RM ;
González-Scarano, F .
VIROLOGY, 2004, 325 (02) :328-339
[4]  
Albright AV, 2000, J NEUROVIROL, V6, pS53
[5]   Annexin II mediates plasminogen-dependent matrix invasion by human monocytes: enhanced expression by macrophages [J].
Brownstein, C ;
Deora, AB ;
Jacovina, AI ;
Weintraub, R ;
Gertler, M ;
Khan, KMF ;
Falcone, DJ ;
Hajjar, KA .
BLOOD, 2004, 103 (01) :317-324
[6]   Modulation of HIV-like particle assembly in vitro by inositol phosphates [J].
Campbell, S ;
Fisher, RJ ;
Towler, EM ;
Fox, S ;
Issaq, HJ ;
Wolfe, T ;
Phillips, LR ;
Rein, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10875-10879
[7]  
CHERTOVA E, 2005, J BIOMOL TECH, V16, P9
[8]  
Diakonova M, 1997, J CELL SCI, V110, P1199
[9]   AP-3 directs the intracellular trafficking of HIV-1 Gag and plays a key role in particle assembly [J].
Dong, XH ;
Li, H ;
Derdowski, A ;
Ding, LM ;
Burnett, A ;
Chen, XM ;
Peters, TR ;
Dermody, TS ;
Woodruff, E ;
Wang, JJ ;
Spearman, P .
CELL, 2005, 120 (05) :663-674
[10]   Annexins in the secretory pathway [J].
Donnelly, SR ;
Moss, SE .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1997, 53 (06) :533-538