To track the behavior of human immunodeficiency virus (HIV)-1 in the cytoplasm of infected cells, we have tagged virions by incorporation of HIV Vpr fused to the GFP. Observation of the GFP-labeled particles in living cells revealed that they moved in curvilinear paths in the cytoplasm and accumulated in the perinuclear region, often near the microtubule-organizing center. Further studies show that HIV uses cytoplasmic dynein and the microtubule network to migrate toward the nucleus. By combining GFP fused to the NH2 terminus of HIV-1 Vpr tagging with other labeling techniques, it was possible to determine the state of progression of individual particles through the viral life cycle. Correlation of immunofluorescent and electron micrographs allowed high resolution imaging of microtubule-associated structures that are proposed to be reverse transcription complexes. Based on these observations, we propose that HIV uses dynein and the microtubule network to facilitate the delivery of the viral genome to the nucleus of the cell during early postentry steps of the HIV life cycle.
Visualization of the intracellular behavior of HIV in living cells
The online version of this article contains supplemental material.
Abbreviations used in this paper: Ad, adenovirus; GFP–Vpr, GFP fused to the NH2 terminus of HIV-1 Vpr; HIV, human immunodeficiency virus; HSV, herpes simplex virus; MOI, multiplicity of infection; MTOC, microtubule-organizing center; PIC, HIV-1 preintegration complex; RTC, reverse transcription complex; VSV-G, vesicular stomatitis virus envelope glycoprotein.
David McDonald, Marie A. Vodicka, Ginger Lucero, Tatyana M. Svitkina, Gary G. Borisy, Michael Emerman, Thomas J. Hope; Visualization of the intracellular behavior of HIV in living cells . J Cell Biol 11 November 2002; 159 (3): 441–452. doi: https://doi.org/10.1083/jcb.200203150
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