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Antiretroviral Drugs Alter the Content of Extracellular Vesicles from HIV-1-Infected Cells.
DeMarino, Catherine; Pleet, Michelle L; Cowen, Maria; Barclay, Robert A; Akpamagbo, Yao; Erickson, James; Ndembi, Nicaise; Charurat, Manhattan; Jumare, Jibreel; Bwala, Sunday; Alabi, Peter; Hogan, Max; Gupta, Archana; Noren Hooten, Nicole; Evans, Michele K; Lepene, Benjamin; Zhou, Weidong; Caputi, Massimo; Romerio, Fabio; Royal, Walter; El-Hage, Nazira; Liotta, Lance A; Kashanchi, Fatah.
Afiliação
  • DeMarino C; Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA, USA.
  • Pleet ML; Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA, USA.
  • Cowen M; Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA, USA.
  • Barclay RA; Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA, USA.
  • Akpamagbo Y; Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA, USA.
  • Erickson J; Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA, USA.
  • Ndembi N; Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Charurat M; Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Jumare J; Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Bwala S; National Hospital, Abuja, Federal Capital Territory, Nigeria.
  • Alabi P; University of Abuja Teaching Hospital, Gwagwalada, Abuja, Nigeria.
  • Hogan M; Systems Biosciences (SBI), Palo Alto, California, USA.
  • Gupta A; Systems Biosciences (SBI), Palo Alto, California, USA.
  • Noren Hooten N; Laboratory of Epidemiology and Population Science, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
  • Evans MK; Laboratory of Epidemiology and Population Science, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
  • Lepene B; Ceres Nanosciences, Inc, Manassas, VA, 20110, USA.
  • Zhou W; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
  • Caputi M; Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL, USA.
  • Romerio F; Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Royal W; Department of Neurology, University of Maryland School of Medicine, Baltimore, MD, USA.
  • El-Hage N; Department of Immunology, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, 33199, USA.
  • Liotta LA; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
  • Kashanchi F; Laboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA, USA. fkashanc@gmu.edu.
Sci Rep ; 8(1): 7653, 2018 05 16.
Article em En | MEDLINE | ID: mdl-29769566
To date, the most effective treatment of HIV-1 is a combination antiretroviral therapy (cART), which reduces viral replication and reverses pathology. We investigated the effect of cART (RT and protease inhibitors) on the content of extracellular vesicles (EVs) released from HIV-1-infected cells. We have previously shown that EVs contain non-coding HIV-1 RNA, which can elicit responses in recipient cells. In this manuscript, we show that TAR RNA levels demonstrate little change with the addition of cART treatment in cell lines, primary macrophages, and patient biofluids. We determined possible mechanisms involved in the selective packaging of HIV-1 RNA into EVs, specifically an increase in EV-associated hnRNP A2/B1. More recent experiments have shown that several other FDA-approved drugs have the ability to alter the content of exosomes released from HIV-1-infected cells. These findings on cART-altered EV content can also be applied to general viral inhibitors (interferons) which are used to treat other chronic infections. Additionally, we describe unique mechanisms of ESCRT pathway manipulation by antivirals, specifically the targeting of VPS4. Collectively, these data imply that, despite antiretroviral therapy, EVs containing viral products are continually released and may cause neurocognitive and immunological dysfunction.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Antirretrovirais / Produtos do Gene tat do Vírus da Imunodeficiência Humana / Vesículas Extracelulares Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Antirretrovirais / Produtos do Gene tat do Vírus da Imunodeficiência Humana / Vesículas Extracelulares Idioma: En Ano de publicação: 2018 Tipo de documento: Article