Quantitative 3D Video Microscopy of HIV Transfer Across T Cell Virological Synapses

Author:

Hübner Wolfgang1234,McNerney Gregory P.1234,Chen Ping1234,Dale Benjamin M.1234,Gordon Ronald E.1234,Chuang Frank Y. S.1234,Li Xiao-Dong1234,Asmuth David M.1234,Huser Thomas1234,Chen Benjamin K.1234

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Immunology Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.

2. Department of Pathology, Mount Sinai School of Medicine, New York, NY 10029, USA.

3. NSF Center for Biophotonics Science and Technology, University of California Davis (UCD), Sacramento, CA 95817, USA.

4. Department of Internal Medicine, University of California Davis Medical Center, Sacramento, CA 95817, USA.

Abstract

The spread of HIV between immune cells is greatly enhanced by cell-cell adhesions called virological synapses, although the underlying mechanisms have been unclear. With use of an infectious, fluorescent clone of HIV, we tracked the movement of Gag in live CD4 T cells and captured the direct translocation of HIV across the virological synapse. Quantitative, high-speed three-dimensional (3D) video microscopy revealed the rapid formation of micrometer-sized “buttons” containing oligomerized viral Gag protein. Electron microscopy showed that these buttons were packed with budding viral crescents. Viral transfer events were observed to form virus-laden internal compartments within target cells. Continuous time-lapse monitoring showed preferential infection through synapses. Thus, HIV dissemination may be enhanced by virological synapse-mediated cell adhesion coupled to viral endocytosis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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