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Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1
BACKGROUND: Completion of HIV life cycle in CD4(+) T lymphocytes needs cell activation. We recently reported that treatment of resting CD4(+) T lymphocytes with exosomes produced by HIV-1 infected cells induces cell activation and susceptibility to HIV replication. Here, we present data regarding th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623921/ https://www.ncbi.nlm.nih.gov/pubmed/26502902 http://dx.doi.org/10.1186/s12977-015-0216-y |
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author | Arenaccio, Claudia Anticoli, Simona Manfredi, Francesco Chiozzini, Chiara Olivetta, Eleonora Federico, Maurizio |
author_facet | Arenaccio, Claudia Anticoli, Simona Manfredi, Francesco Chiozzini, Chiara Olivetta, Eleonora Federico, Maurizio |
author_sort | Arenaccio, Claudia |
collection | PubMed |
description | BACKGROUND: Completion of HIV life cycle in CD4(+) T lymphocytes needs cell activation. We recently reported that treatment of resting CD4(+) T lymphocytes with exosomes produced by HIV-1 infected cells induces cell activation and susceptibility to HIV replication. Here, we present data regarding the effects of these exosomes on cells latently infected with HIV-1. RESULTS: HIV-1 latently infecting U937-derived U1 cells was activated upon challenge with exosomes purified from the supernatant of U937 cells chronically infected with HIV-1. This effect was no more detectable when exosomes from cells infected with HIV-1 strains either nef-deleted or expressing a functionally defective Nef were used, indicating that Nef is the viral determinant of exosome-induced HIV-1 activation. Treatment with either TAPI-2, i.e., a specific inhibitor of the pro-TNFα-processing ADAM17 enzyme, or anti-TNFα Abs abolished HIV-1 activation. Hence, similar to what previously demonstrated for the exosome-mediated activation of uninfected CD4(+) T lymphocytes, the Nef-ADAM17-TNFα axis is part of the mechanism of latent HIV-1 activation. It is noteworthy that these observations have been reproduced using: (1) primary CD4(+) T lymphocytes latently infected with HIV-1; (2) exosomes from both primary CD4(+) T lymphocytes and macrophages acutely infected with HIV-1; (3) co-cultures of HIV-1 acutely infected CD4(+) T lymphocytes and autologous lymphocytes latently infected with HIV-1, and (4) exosomes from cells expressing a defective HIV-1. CONCLUSIONS: Our results strongly suggest that latent HIV-1 can be activated by TNFα released by cells upon ingestion of exosomes released by infected cells, and that this effect depends on the activity of exosome-associated ADAM17. These pieces of evidence shed new light on the mechanism of HIV reactivation in latent reservoirs, and might also be relevant to design new therapeutic interventions focused on HIV eradication. |
format | Online Article Text |
id | pubmed-4623921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46239212015-10-29 Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1 Arenaccio, Claudia Anticoli, Simona Manfredi, Francesco Chiozzini, Chiara Olivetta, Eleonora Federico, Maurizio Retrovirology Research BACKGROUND: Completion of HIV life cycle in CD4(+) T lymphocytes needs cell activation. We recently reported that treatment of resting CD4(+) T lymphocytes with exosomes produced by HIV-1 infected cells induces cell activation and susceptibility to HIV replication. Here, we present data regarding the effects of these exosomes on cells latently infected with HIV-1. RESULTS: HIV-1 latently infecting U937-derived U1 cells was activated upon challenge with exosomes purified from the supernatant of U937 cells chronically infected with HIV-1. This effect was no more detectable when exosomes from cells infected with HIV-1 strains either nef-deleted or expressing a functionally defective Nef were used, indicating that Nef is the viral determinant of exosome-induced HIV-1 activation. Treatment with either TAPI-2, i.e., a specific inhibitor of the pro-TNFα-processing ADAM17 enzyme, or anti-TNFα Abs abolished HIV-1 activation. Hence, similar to what previously demonstrated for the exosome-mediated activation of uninfected CD4(+) T lymphocytes, the Nef-ADAM17-TNFα axis is part of the mechanism of latent HIV-1 activation. It is noteworthy that these observations have been reproduced using: (1) primary CD4(+) T lymphocytes latently infected with HIV-1; (2) exosomes from both primary CD4(+) T lymphocytes and macrophages acutely infected with HIV-1; (3) co-cultures of HIV-1 acutely infected CD4(+) T lymphocytes and autologous lymphocytes latently infected with HIV-1, and (4) exosomes from cells expressing a defective HIV-1. CONCLUSIONS: Our results strongly suggest that latent HIV-1 can be activated by TNFα released by cells upon ingestion of exosomes released by infected cells, and that this effect depends on the activity of exosome-associated ADAM17. These pieces of evidence shed new light on the mechanism of HIV reactivation in latent reservoirs, and might also be relevant to design new therapeutic interventions focused on HIV eradication. BioMed Central 2015-10-26 /pmc/articles/PMC4623921/ /pubmed/26502902 http://dx.doi.org/10.1186/s12977-015-0216-y Text en © Arenaccio et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Arenaccio, Claudia Anticoli, Simona Manfredi, Francesco Chiozzini, Chiara Olivetta, Eleonora Federico, Maurizio Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1 |
title | Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1 |
title_full | Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1 |
title_fullStr | Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1 |
title_full_unstemmed | Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1 |
title_short | Latent HIV-1 is activated by exosomes from cells infected with either replication-competent or defective HIV-1 |
title_sort | latent hiv-1 is activated by exosomes from cells infected with either replication-competent or defective hiv-1 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623921/ https://www.ncbi.nlm.nih.gov/pubmed/26502902 http://dx.doi.org/10.1186/s12977-015-0216-y |
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