Cited by 184HIV Research and TreatmentHIV/AIDS Research and InterventionsT-cell and Retrovirus Studies

3D visualization of HIV transfer at the virological synapse between dendritic cells and T cells

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Felts, Richard L., Narayan, Kedar, Estes, Jacob D., Shi, Dan, Trubey, Charles M., Fu, Jing, Hartnell, Lisa M., Ruthel, Gordon T. +8 more·2010·Proceedings of the National Academy of Sciences

Abstract

The efficiency of HIV infection is greatly enhanced when the virus is delivered at conjugates between CD4 + T cells and virus-bearing antigen-presenting cells such as macrophages or dendritic cells via specialized structures known as virological synapses. Using ion abrasion SEM, electron tomography, and superresolution light microscopy, we have analyzed the spatial architecture of cell-cell contacts and distribution of HIV virions at virological synapses formed between mature dendritic cells and T cells. We demonstrate the striking envelopment of T cells by sheet-like membrane extensions derived from mature dendritic cells, resulting in a shielded region for formation of virological synapses. Within the synapse, filopodial extensions emanating from CD4 + T cells make contact with HIV virions sequestered deep within a 3D network of surface-accessible compartments in the dendritic cell. Viruses are detected at the membrane surfaces of both dendritic cells and T cells, but virions are not released passively at the synapse; instead, virus transfer requires the engagement of T-cell CD4 receptors. The relative seclusion of T cells from the extracellular milieu, the burial of the site of HIV transfer, and the receptor-dependent initiation of virion transfer by T cells highlight unique aspects of cell-cell HIV transmission.

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Crossref · 10.1073/pnas.1003040107

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6 of 6 references verified0 citation errors · 0 not checkable

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  • Membrane extensions derived from DCs envelop the T cell and shield the synapse zone, and filopodial extensions from T cells contact virions deep inside DC plasma membrane invaginations.

    “Their study revealed membrane extensions derived from DCs that enveloped the T cell, and shielded the synapse zone. Furthermore, filopodial extensions emanating from T cells that contacted virions located deep inside the invaginations of the DC plasma membrane were visualized [90].”
  • The interaction of Env with CD4 is necessary for the transfer of HIV-1 viral particles across the synaptic cleft towards the target cell.

    “However, the interaction of Env with CD4 is necessary for the transfer of HIV-1 viral particles across the synaptic cleft towards the target cell [90].”

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Authors
Felts, R. L., Narayan, K., Estes, J. D., Shi, D., Trubey, C. M., Fu, J., Hartnell, L. M., Ruthel, G. T., Schneider, D. K., Nagashima, K., Bess, J. W., Bavari, S., Lowekamp, B. C., Bliss, D., Lifson, J. D., & Subramaniam, S.
Affiliations
  • National Institutes of Health (US)
  • United States Army Medical Research Institute of Infectious Diseases (US)
  • National Cancer Institute (US)
Venue
Proceedings of the National Academy of Sciences
Published
2010-07-12
Volume
107
Issue
30
Pages
13336-13341
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W1996939435
Cited by
184
References
6
Citations by year
2026: 2 · 2025: 1 · 2024: 7 · 2023: 7 · 2022: 13 · 2021: 6 · 2020: 4 · 2019: 9 · 2018: 14 · 2017: 16 · 2016: 10 · 2015: 18 · 2014: 18 · 2013: 13 · 2012: 26
FWCI
6.65
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (HHSN261200800001C)
  • National Cancer Institute (Contract HHSN261200800001E, HHSN261200800001E))
  • National Institute of General Medical Sciences
Topics
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
  • Health Sciences › Medicine › Infectious Diseases › HIV/AIDS Research and Interventions
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
Keywords
virological synapse, dendritic cells, CD4+ T cells, cell-cell contact, filopodia, CD4 receptor, virus transmission, three-dimensional cell structure
MeSH terms
Antigen-Presenting Cells, Cell Communication, Dendritic Cells, HIV, Humans, Microscopy, Electron, Scanning, Microscopy, Fluorescence, T-Lymphocytes, Virion, CD4-Positive T-Lymphocytes, Microscopy, Electron, Transmission, Host-Pathogen Interactions

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