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Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses
Extracellular vesicles (EVs) or exosomes have been implicated in the pathophysiology of infections and cancer. The negative regulatory factor (Nef) encoded by simian immunodeficiency virus (SIV) and human immunodeficiency virus (HIV) plays a critical role in the progression to AIDS and impairs endos...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801467/ https://www.ncbi.nlm.nih.gov/pubmed/29437924 http://dx.doi.org/10.1128/mBio.02344-17 |
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author | McNamara, Ryan P. Costantini, Lindsey M. Myers, T. Alix Schouest, Blake Maness, Nicholas J. Griffith, Jack D. Damania, Blossom A. MacLean, Andrew G. Dittmer, Dirk P. |
author_facet | McNamara, Ryan P. Costantini, Lindsey M. Myers, T. Alix Schouest, Blake Maness, Nicholas J. Griffith, Jack D. Damania, Blossom A. MacLean, Andrew G. Dittmer, Dirk P. |
author_sort | McNamara, Ryan P. |
collection | PubMed |
description | Extracellular vesicles (EVs) or exosomes have been implicated in the pathophysiology of infections and cancer. The negative regulatory factor (Nef) encoded by simian immunodeficiency virus (SIV) and human immunodeficiency virus (HIV) plays a critical role in the progression to AIDS and impairs endosomal trafficking. Whether HIV-1 Nef can be loaded into EVs has been the subject of controversy, and nothing is known about the connection between SIV Nef and EVs. We find that both SIV and HIV-1 Nef proteins are present in affinity-purified EVs derived from cultured cells, as well as in EVs from SIV-infected macaques. Nef-positive EVs were functional, i.e., capable of membrane fusion and depositing their content into recipient cells. The EVs were able to transfer Nef into recipient cells. This suggests that Nef readily enters the exosome biogenesis pathway, whereas HIV virions are assembled at the plasma membrane. It suggests a novel mechanism by which lentiviruses can influence uninfected and uninfectable, i.e., CD4-negative, cells. |
format | Online Article Text |
id | pubmed-5801467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-58014672018-02-12 Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses McNamara, Ryan P. Costantini, Lindsey M. Myers, T. Alix Schouest, Blake Maness, Nicholas J. Griffith, Jack D. Damania, Blossom A. MacLean, Andrew G. Dittmer, Dirk P. mBio Research Article Extracellular vesicles (EVs) or exosomes have been implicated in the pathophysiology of infections and cancer. The negative regulatory factor (Nef) encoded by simian immunodeficiency virus (SIV) and human immunodeficiency virus (HIV) plays a critical role in the progression to AIDS and impairs endosomal trafficking. Whether HIV-1 Nef can be loaded into EVs has been the subject of controversy, and nothing is known about the connection between SIV Nef and EVs. We find that both SIV and HIV-1 Nef proteins are present in affinity-purified EVs derived from cultured cells, as well as in EVs from SIV-infected macaques. Nef-positive EVs were functional, i.e., capable of membrane fusion and depositing their content into recipient cells. The EVs were able to transfer Nef into recipient cells. This suggests that Nef readily enters the exosome biogenesis pathway, whereas HIV virions are assembled at the plasma membrane. It suggests a novel mechanism by which lentiviruses can influence uninfected and uninfectable, i.e., CD4-negative, cells. American Society for Microbiology 2018-02-06 /pmc/articles/PMC5801467/ /pubmed/29437924 http://dx.doi.org/10.1128/mBio.02344-17 Text en Copyright © 2018 McNamara et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article McNamara, Ryan P. Costantini, Lindsey M. Myers, T. Alix Schouest, Blake Maness, Nicholas J. Griffith, Jack D. Damania, Blossom A. MacLean, Andrew G. Dittmer, Dirk P. Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses |
title | Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses |
title_full | Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses |
title_fullStr | Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses |
title_full_unstemmed | Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses |
title_short | Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses |
title_sort | nef secretion into extracellular vesicles or exosomes is conserved across human and simian immunodeficiency viruses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801467/ https://www.ncbi.nlm.nih.gov/pubmed/29437924 http://dx.doi.org/10.1128/mBio.02344-17 |
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