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Exosomes Derived from HIV-1-infected Cells Contain Trans-activation Response Element RNA
Open accessAbstract
Exosomes are nano-sized vesicles produced by healthy and virus-infected cells. Exosomes derived from infected cells have been shown to contain viral microRNAs (miRNAs). HIV-1 encodes its own miRNAs that regulate viral and host gene expression. The most abundant HIV-1-derived miRNA, first reported by us and later by others using deep sequencing, is the trans-activation response element (TAR) miRNA. In this study, we demonstrate the presence of TAR RNA in exosomes from cell culture supernatants of HIV-1-infected cells and patient sera. TAR miRNA was not in Ago2 complexes outside the exosomes but enclosed within the exosomes. We detected the host miRNA machinery proteins Dicer and Drosha in exosomes from infected cells. We report that transport of TAR RNA from the nucleus into exosomes is a CRM1 (chromosome region maintenance 1)-dependent active process. Prior exposure of naive cells to exosomes from infected cells increased susceptibility of the recipient cells to HIV-1 infection. Exosomal TAR RNA down-regulated apoptosis by lowering Bim and Cdk9 proteins in recipient cells. We found 10 4 –10 6 copies/ml TAR RNA in exosomes derived from infected culture supernatants and 10 3 copies/ml TAR RNA in the serum exosomes of highly active antiretroviral therapy-treated patients or long term nonprogressors. Taken together, our experiments demonstrated that HIV-1-infected cells produced exosomes that are uniquely characterized by their proteomic and RNA profiles that may contribute to disease pathology in AIDS. Background: Exosomes are extracellular vesicles that have been implicated in intercellular communication. Results: Exosomes that originate from human cells infected with HIV-1 contain virus-derived small noncoding RNA. Conclusion: Virus-derived small RNA present in exosomes exert functional consequences in naive recipient cells. Significance: Viral RNA molecules present in exosomes may be critical mediators of intercellular viral spread in infected hosts.
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“It was reported that exosomes secreted by HIV-1-infected cells contained a trans-activation response element (TAR), an RNA structure involved in the activation of the viral 5′-LTR promoter, as well as cellular RNase III enzymes, Dicer and Drosha. Incubation with such exosomes increased the permissiveness of recipient cells to HIV-1 infection, and inhibited the apoptosis of infected cells [126].”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [126]
Citations
Cites
Bartel (2004) · doi:10.1016/s0092-8674(04)00045-5 · Cited by 34,714
Valadi, H., Ekström, K., Bossios, A., Sjöstrand, M., Lee, J. J., & Lötvall, J. O. (2007) · Nature Cell Biology · doi:10.1038/ncb1596 · Cited by 12,834
The nuclear RNase III Drosha initiates microRNA processing
Lee, Y., Ahn, C., Han, J., Choi, H., Kim, J., Yim, J., Lee, J., Provost, P., Rådmark, O., Kim, S., et al. (2003) · Nature · doi:10.1038/nature01957 · Cited by 5,299
Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes
Alvarez-Erviti, L., Seow, Y., Yin, H., Betts, C., Lakhal, S., & Wood, M. J. A. (2011) · Nature Biotechnology · doi:10.1038/nbt.1807 · Cited by 4,930
Membrane vesicles as conveyors of immune responses
Théry, C., Ostrowski, M., & Segura, É. (2009) · Nature reviews. Immunology · doi:10.1038/nri2567 · Cited by 3,996
Ceramide Triggers Budding of Exosome Vesicles into Multivesicular Endosomes
Trajković, K., Hsu, C., Chiantia, S., Rajendran, L., Wenzel, D., Wieland, F., Schwille, P., Brügger, B., & Simons, M. (2008) · Science · doi:10.1126/science.1153124 · Cited by 3,760
Arroyo, J. D., Chevillet, J. R., Kroh, E. M., Ruf, I. K., Pritchard, C. C., Gibson, D. F., Mitchell, P. S., Bennett, C. F., Pogosova-Agadjanyan, E. L., Stirewalt, D. L., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019055108 · Cited by 3,294
Many roads to maturity: microRNA biogenesis pathways and their regulation
Winter, J. J., Jung, S., Keller, S., Gregory, R. I., & Diederichs, S. (2009) · Nature Cell Biology · doi:10.1038/ncb0309-228 · Cited by 2,765
Exosomes: Extracellular organelles important in intercellular communication
Mathivanan, S., Ji, H. L., & Simpson, R. J. (2010) · Journal of Proteomics · doi:10.1016/j.jprot.2010.06.006 · Cited by 2,581
Small silencing RNAs: an expanding universe
Ghildiyal, M., & Zamore, P. D. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2504 · Cited by 2,418
Flagged first, then by citations
3 of the 95 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Carpio, 2010, microRNA machinery is an integral component of drug-induced transcription inhibition in HIV-1 infection, J. RNAi Gene Silencing, 6, 386
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Items 201–300 of 316
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Hadifar, S., Fateh, A., Yousefi, M. H., Siadat, S. D., & Vaziri, F. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27555 · Cited by 14
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Chen, Y., Wang, T., Yang, Y., Fang, Y., Zhao, B. Y., Zeng, W., Lv, D., Zhang, L., Zhang, Y., Xue, Q., et al. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010759 · Cited by 13
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DeMarino, C., Barclay, R. A., Pleet, M. L., Pinto, D. O., Branscome, H., Paul, S., Lepene, B. S., El‐Hage, N., & Kashanchi, F. (2019) · Journal of Visualized Experiments · doi:10.3791/59876 · Cited by 12
Self-citationDeMarino, C., Cowen, M., Pleet, M. L., Pinto, D. O., Khatkar, P., Erickson, J. W., Docken, S. S., Russell, N., Reichmuth, B., Phan, T., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-59008-0 · Cited by 11
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Pinto, D. O., DeMarino, C., Vo, T. T., Cowen, M., Kim, Y., Pleet, M. L., Barclay, R. A., Hooten, N. N., Evans, M. K., Heredia, A., et al. (2020) · Viruses · doi:10.3390/v12080885 · Cited by 10
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Self-citationMolnar, S., Kim, Y., Wieczorek, L., Williams, A., Patil, K., Khatkar, P., Santos, M. F., Mensah, G. A., Lorico, A., Polonis, V. R., et al. (2024) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12476 · Cited by 8
Self-citationLi, S., Bu, J., Pan, X., Li, Q., Zuo, X., Xiao, G., Du, J., Zhang, L., Xia, B., & Gao, Z. (2024) · Journal of Medical Virology · doi:10.1002/jmv.29782 · Cited by 8
Dweep, H., Gretz, N., & Felekkis, K. N. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-1062-5_26 · Cited by 8
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Sharma, D., Srivastava, S., & Babu, M. R. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-10639-4 · Cited by 8
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Zhao, Y., Chen, H., Du, C., Jian, Y., Li, H., Xiao, Y., Saifuddin, M., Kashanchi, F., & Zeng, C. (2018) · International Journal of Peptide Research and Therapeutics · doi:10.1007/s10989-018-9730-9 · Cited by 7
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Mizenko, R. R., Brostoff, T., Jackson, K., Pesavento, P. A., & Carney, R. P. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.01211-22 · Cited by 7
Barrios, M. H., Garnham, A. L., Foers, A. D., Cheng, L., Masters, S. L., & Pang, K. C. (2021) · Biomedicines · doi:10.3390/biomedicines9091136 · Cited by 7
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Haque, S., Kodidela, S., Gerth, K. A., Hatami, E., Verma, N., & Kumar, S. (2020) · Vide Leaf, Hyderabad eBooks · doi:10.37247/pamb.1.2020.51 · Cited by 6
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Self-citationSampey, G. C., Iordanskiy, S., Pleet, M. L., DeMarino, C., Romerio, F., Mahieux, R., & Kashanchi, F. (2020) · Viruses · doi:10.3390/v12101067 · Cited by 6
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Self-citationSharma, N. K. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04770-2 · Cited by 6
Chistiakov, D. A., Grechko, A. V., Orekhov, A. N., & Bobryshev, Y. V. (2017) · Annals of Translational Medicine · doi:10.21037/atm.2017.06.34 · Cited by 6
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Chandra, P. K., Braun, S. E., Maity, S., Castorena‐Gonzalez, J. A., Kim, H., Shaffer, J. G., Čikić, S., Rutkai, I., Fan, J., Guidry, J. J., et al. (2023) · Viruses · doi:10.3390/v15030794 · Cited by 5
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Yang, J., Feng, Z., McComsey, G. A., Avery, A., Hileman, C. O., Xiong, W., Alban, T. J., Jin, G., & Wang, B. (2026) · Journal of NeuroVirology · doi:10.1007/s13365-025-01297-0 · Cited by 2
Sberna, G., Nardacci, R., Berno, G., Rozera, G., Giombini, E., Fabeni, L., Specchiarello, E., Maggi, F., & Amendola, A. (2023) · Journal of Clinical Virology · doi:10.1016/j.jcv.2023.105575 · Cited by 2
Boucher, J., Bazié, W. W., Goyer, B., Alary, M., & Gilbert, C. (2025) · Journal of Medical Virology · doi:10.1002/jmv.70574 · Cited by 3
Self-citationChanda, D., del Rivero, T., Ghimire, R., More, S., Mitrani, M. I., Bellio, M. A., & Channappanavar, R. (2024) · Viruses · doi:10.3390/v16020273 · Cited by 2
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Mao, L., Gao, Q., Shen, Y., Bao, C., Xiang, H., Chen, Q., Gao, Q., Huang, F., He, W., & Wang, J. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1430052 · Cited by 1
Biswas, U., Bernal, C., Wang, R., & DeStefano, J. J. (2025) · Journal of Virology · doi:10.1128/jvi.00564-25 · Cited by 1
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Kapoor, N., & Kumar, V. (2014) · International Journal of Biochemistry Research & Review · doi:10.9734/ijbcrr/2014/9370 · Cited by 1
Boucher, J., Bazié, W. W., Goyer, B., Alary, M., & Gilbert, C. (2024) · medRxiv · doi:10.1101/2024.11.01.24316593 · Cited by 1
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Arbuthnot, P. B. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-410518-8.00008-9
Ansari, M. Y., Imam, H., Kumar, N., Ahmed, Z., & Jameel, S. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/148791
Chen, L., Feng, Z., Yuan, G., Reinthal, B., Ye, F., & Jin, G. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/640532
Otaguiri, K. K. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.60.2019.tde-23052019-072849
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Mensah, G. A. (2019) · doi:10.13021/mars/7211
Phan, T., DeMarino, C., Kashanchi, F., Kuang, Y., Anderson, D. M., & Emelianenko, M. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2005.11343
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Margaroli, C., & Russell, D. W. (2021) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2021-0222ed
Phan, T., DeMarino, C., Kashanchi, F., Kuang, Y., Anderson, D., & Emelianenko, M. (2021) · Letters in Biomathematics · doi:10.30707/lib8.1.1647878866.063128
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Bellotti, C., Stäuble, A., & Steinfeld, R. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264642
Kumar, S. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736559137.793566863
Kumar, S. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718345487.793578787
Baldari, C. T., & Finetti, F. (2017) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718505292.793537779
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Tiberi, L. V., Matteo, A. D., Palma, F. D. E. D., Lizarralde-Guerrero, M., Djavaheri‐Mergny, M., Vitale, M., Scialó, F., Pastore, L., Maiuri, M. C., & Pol, J. G. (2025) · International review of cytology · doi:10.1016/bs.ircmb.2025.12.002
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Metadata
- Authors
- Narayanan, A., Iordanskiy, S., Das, R., Van Duyne, R., Santos, S., Jaworski, E., Guendel, I., Sampey, G., Dalby, E., Iglesias-Ussel, M., Popratiloff, A., Hakami, R., Kehn-Hall, K., Young, M., Subra, C., Gilbert, C., Bailey, C., Romerio, F., & Kashanchi, F.
- Affiliations
- George Mason University (US)
- George Washington University (US)
- University of Maryland, Baltimore (US)
- Georgetown University Medical Center (US)
- Centre hospitalier de l'Université Laval (CA)
- Corresponding author
- Kashanchi, Fatah
- ORCID
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2013-07
- Volume
- 288
- Issue
- 27
- Pages
- 20014-20033
- ISSN
- 0021-9258 (ISSN-L)
- PMC
- PMC3707700
- OpenAlex
- W1991259997
- Cited by
- 316
- References
- 95
- Citations by year
- 2026: 11 · 2025: 13 · 2024: 29 · 2023: 20 · 2022: 18 · 2021: 39 · 2020: 34 · 2019: 31 · 2018: 27 · 2017: 26 · 2016: 26 · 2015: 21 · 2014: 17 · 2013: 4
- FWCI
- 10.16
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (P30AI087714, UO1-AI35004, UO1AI34993, R21AI078859, AI 078859, UO1-AI31834, AI074410, U01AI034989, U01AI031834, U01AI042590, R01AI043894, UO1-AI-34989, U01AI034993, U01AI034994, AI043894, R21AI074410, U01AI035004, UO1-AI-34994, UO1-AI-42590)
- National Center for Research Resources (UL1RR024131)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (UO1-HD-32632, U01HD032632)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Keywords
- exosomes, HIV-1, TAR RNA, viral microRNAs, extracellular vesicles, CRM1, Dicer, Drosha, Argonaute 2, apoptosis, building information modeling, CDK9, HIV-1 infection susceptibility, long-term nonprogressors, antiretroviral therapy, serum exosomes
- MeSH terms
- Bcl-2-Like Protein 11, Acquired Immunodeficiency Syndrome, HeLa Cells, Humans, Membrane Proteins, Proto-Oncogene Proteins, RNA, Viral, HIV-1, Down-Regulation, HIV Long Terminal Repeat, Cyclin-Dependent Kinase 9, Apoptosis Regulatory Proteins, Exosomes
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