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HIV-1 Virological Synapse is not Simply a Copycat of the Immunological Synapse
Program in Molecular Pathogenesis, Martin and Helen Kimmel Center for Biology and Medicine, Skirball Institute for Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA
Veterans Affairs New York Harbor Healthcare System, Manhattan Campus, Department of Pathology, New York University School of Medicine, New York, NY 10010, USA
* Authors to whom correspondence should be addressed.
Received: 3 March 2010; in revised form: 5 May 2010 / Accepted: 12 May 2010 / Published: 21 May 2010
Abstract: The virological synapse (VS) is a tight adhesive junction between an HIV-infected cell and an uninfected target cell, across which virus can be efficiently transferred from cell to cell in the absence of cell-cell fusion. The VS has been postulated to resemble, in its morphology, the well-studied immunological synapse (IS). This review article discusses the structural similarities between IS and VS and the shared T cell receptor (TCR) signaling components that are found in the VS. However, the IS and the VS display distinct kinetics in disassembly and intracellular signaling events, possibly leading to different biological outcomes. Hence, HIV-1 exploits molecular components of IS and TCR signaling machinery to trigger unique changes in cellular morphology, migration, and activation that facilitate its transmission and cell-to-cell spread.
Keywords: HIV-1; HIV; virological synapse; immunological synapse; HIV envelope; gp120; T cell receptor; CD4 T lymphocyte
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Vasiliver-Shamis, G.; Dustin, M.L.; Hioe, C.E. HIV-1 Virological Synapse is not Simply a Copycat of the Immunological Synapse. Viruses 2010, 2, 1239-1260.
Vasiliver-Shamis G, Dustin ML, Hioe CE. HIV-1 Virological Synapse is not Simply a Copycat of the Immunological Synapse. Viruses. 2010; 2(5):1239-1260.
Vasiliver-Shamis, Gaia; Dustin, Michael L.; Hioe, Catarina E. 2010. "HIV-1 Virological Synapse is not Simply a Copycat of the Immunological Synapse." Viruses 2, no. 5: 1239-1260.