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The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells

INTRODUCTION: The HIV Nef protein is a multifunctional virulence factor that perturbs intracellular membranes and signalling and is secreted into exosomes. While Nef-containing exosomes have a distinct proteomic profile, no comprehensive analysis of their miRNA cargo has been carried out. Since Nef...

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Autores principales: Aqil, Madeeha, Naqvi, Afsar Raza, Mallik, Saurav, Bandyopadhyay, Sanghamitra, Maulik, Ujjwal, Jameel, Shahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967016/
https://www.ncbi.nlm.nih.gov/pubmed/24678387
http://dx.doi.org/10.3402/jev.v3.23129
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author Aqil, Madeeha
Naqvi, Afsar Raza
Mallik, Saurav
Bandyopadhyay, Sanghamitra
Maulik, Ujjwal
Jameel, Shahid
author_facet Aqil, Madeeha
Naqvi, Afsar Raza
Mallik, Saurav
Bandyopadhyay, Sanghamitra
Maulik, Ujjwal
Jameel, Shahid
author_sort Aqil, Madeeha
collection PubMed
description INTRODUCTION: The HIV Nef protein is a multifunctional virulence factor that perturbs intracellular membranes and signalling and is secreted into exosomes. While Nef-containing exosomes have a distinct proteomic profile, no comprehensive analysis of their miRNA cargo has been carried out. Since Nef functions as a viral suppressor of RNA interference and disturbs the distribution of RNA-induced silencing complex proteins between cells and exosomes, we hypothesized that it might also affect the export of miRNAs into exosomes. METHOD: Exosomes were purified from human monocytic U937 cells that stably expressed HIV-1 Nef. The RNA from cells and exosomes was profiled for 667 miRNAs using a Taqman Low Density Array. Selected miRNAs and their mRNA targets were validated by quantitative RT-PCR. Bioinformatics analyses were used to identify targets and predict pathways. RESULTS: Nef expression affected a significant fraction of miRNAs in U937 cells. Our analysis showed 47 miRNAs to be selectively secreted into Nef exosomes and 2 miRNAs to be selectively retained in Nef-expressing cells. The exosomal miRNAs were predicted to target several cellular genes in inflammatory cytokine and other pathways important for HIV pathogenesis, and an overwhelming majority had targets within the HIV genome. CONCLUSIONS: This is the first study to report miRnome analysis of HIV Nef expressing monocytes and exosomes. Our results demonstrate that Nef causes large-scale dysregulation of cellular miRNAs, including their secretion through exosomes. We suggest this to be a novel viral strategy to affect pathogenesis and to limit the effects of RNA interference on viral replication and persistence.
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spelling pubmed-39670162014-03-27 The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells Aqil, Madeeha Naqvi, Afsar Raza Mallik, Saurav Bandyopadhyay, Sanghamitra Maulik, Ujjwal Jameel, Shahid J Extracell Vesicles Original Research Article INTRODUCTION: The HIV Nef protein is a multifunctional virulence factor that perturbs intracellular membranes and signalling and is secreted into exosomes. While Nef-containing exosomes have a distinct proteomic profile, no comprehensive analysis of their miRNA cargo has been carried out. Since Nef functions as a viral suppressor of RNA interference and disturbs the distribution of RNA-induced silencing complex proteins between cells and exosomes, we hypothesized that it might also affect the export of miRNAs into exosomes. METHOD: Exosomes were purified from human monocytic U937 cells that stably expressed HIV-1 Nef. The RNA from cells and exosomes was profiled for 667 miRNAs using a Taqman Low Density Array. Selected miRNAs and their mRNA targets were validated by quantitative RT-PCR. Bioinformatics analyses were used to identify targets and predict pathways. RESULTS: Nef expression affected a significant fraction of miRNAs in U937 cells. Our analysis showed 47 miRNAs to be selectively secreted into Nef exosomes and 2 miRNAs to be selectively retained in Nef-expressing cells. The exosomal miRNAs were predicted to target several cellular genes in inflammatory cytokine and other pathways important for HIV pathogenesis, and an overwhelming majority had targets within the HIV genome. CONCLUSIONS: This is the first study to report miRnome analysis of HIV Nef expressing monocytes and exosomes. Our results demonstrate that Nef causes large-scale dysregulation of cellular miRNAs, including their secretion through exosomes. We suggest this to be a novel viral strategy to affect pathogenesis and to limit the effects of RNA interference on viral replication and persistence. Co-Action Publishing 2014-03-25 /pmc/articles/PMC3967016/ /pubmed/24678387 http://dx.doi.org/10.3402/jev.v3.23129 Text en © 2014 Madeeha Aqil et al. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Aqil, Madeeha
Naqvi, Afsar Raza
Mallik, Saurav
Bandyopadhyay, Sanghamitra
Maulik, Ujjwal
Jameel, Shahid
The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells
title The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells
title_full The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells
title_fullStr The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells
title_full_unstemmed The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells
title_short The HIV Nef protein modulates cellular and exosomal miRNA profiles in human monocytic cells
title_sort hiv nef protein modulates cellular and exosomal mirna profiles in human monocytic cells
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967016/
https://www.ncbi.nlm.nih.gov/pubmed/24678387
http://dx.doi.org/10.3402/jev.v3.23129
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