3D visualization of HIV transfer at the virological synapse between dendritic cells and T cells
Open accessAbstract
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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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].”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [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].”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [90]
Cites
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Wilen, C. B., Tilton, J. C., & Doms, R. W. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006866 · Cited by 654 · see citing works
HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread
Kalinichenko, S., Komkov, D., & Mazurov, D. (2022) · Viruses · doi:10.3390/v14010152 · Cited by 68 · see citing works
“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].”
Background
- 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)
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2010-07-12
- Volume
- 107
- Issue
- 30
- Pages
- 13336-13341
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2922156
- 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
- green
- www.ncbi.nlm.nih.gov
- 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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