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Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles

Elevated TLR expression/signalling in monocyte/macrophages has been shown to mediate systemic immune activation, a hallmark of progressive HIV-1 infection. Here we show, via differential gene expression comparisons, the presence of a constitutive in vivo TLR-like gene activation signature in steady-...

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Autores principales: Gekonge, Bethsebah, Giri, Malavika S., Kossenkov, Andrew V., Nebozyhn, Michael, Yousef, Malik, Mounzer, Karam, Showe, Louise, Montaner, Luis J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399809/
https://www.ncbi.nlm.nih.gov/pubmed/22815948
http://dx.doi.org/10.1371/journal.pone.0041153
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author Gekonge, Bethsebah
Giri, Malavika S.
Kossenkov, Andrew V.
Nebozyhn, Michael
Yousef, Malik
Mounzer, Karam
Showe, Louise
Montaner, Luis J.
author_facet Gekonge, Bethsebah
Giri, Malavika S.
Kossenkov, Andrew V.
Nebozyhn, Michael
Yousef, Malik
Mounzer, Karam
Showe, Louise
Montaner, Luis J.
author_sort Gekonge, Bethsebah
collection PubMed
description Elevated TLR expression/signalling in monocyte/macrophages has been shown to mediate systemic immune activation, a hallmark of progressive HIV-1 infection. Here we show, via differential gene expression comparisons, the presence of a constitutive in vivo TLR-like gene activation signature in steady-state circulating monocytes from chronically HIV-1 infected subjects. The TLR2-like gene signature was defined as an 82 gene subset of the 376 genes constitutively modulated in in vivo HIV-1 monocytes, based on their overlap with de novo TLR2-induced genes in uninfected subjects’ monocytes following acute ex vivo stimulation with Staphylococcus Aureus Cowan (SAC). Additional comparison of in vivo gene networks with available datasets from acute TLR activations in M/M expanded the overlap to 151-gene concordance among the 376 differential genes with emphasis on ERK/MAPK, TNF/IL6 (NFκB) and p53 gene networks. TLR2 stimulation of monocytes from HIV-1 infected subjects resulted in further upregulation of inflammatory genes indicative of a sustained transcriptional potential upon stimulation. In summary, our data support the presence of a sustained TLR-like gene activation profile in circulating monocyte from steady-state viremia in HIV-1 infected subjects.
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spelling pubmed-33998092012-07-19 Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles Gekonge, Bethsebah Giri, Malavika S. Kossenkov, Andrew V. Nebozyhn, Michael Yousef, Malik Mounzer, Karam Showe, Louise Montaner, Luis J. PLoS One Research Article Elevated TLR expression/signalling in monocyte/macrophages has been shown to mediate systemic immune activation, a hallmark of progressive HIV-1 infection. Here we show, via differential gene expression comparisons, the presence of a constitutive in vivo TLR-like gene activation signature in steady-state circulating monocytes from chronically HIV-1 infected subjects. The TLR2-like gene signature was defined as an 82 gene subset of the 376 genes constitutively modulated in in vivo HIV-1 monocytes, based on their overlap with de novo TLR2-induced genes in uninfected subjects’ monocytes following acute ex vivo stimulation with Staphylococcus Aureus Cowan (SAC). Additional comparison of in vivo gene networks with available datasets from acute TLR activations in M/M expanded the overlap to 151-gene concordance among the 376 differential genes with emphasis on ERK/MAPK, TNF/IL6 (NFκB) and p53 gene networks. TLR2 stimulation of monocytes from HIV-1 infected subjects resulted in further upregulation of inflammatory genes indicative of a sustained transcriptional potential upon stimulation. In summary, our data support the presence of a sustained TLR-like gene activation profile in circulating monocyte from steady-state viremia in HIV-1 infected subjects. Public Library of Science 2012-07-18 /pmc/articles/PMC3399809/ /pubmed/22815948 http://dx.doi.org/10.1371/journal.pone.0041153 Text en Gekonge et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gekonge, Bethsebah
Giri, Malavika S.
Kossenkov, Andrew V.
Nebozyhn, Michael
Yousef, Malik
Mounzer, Karam
Showe, Louise
Montaner, Luis J.
Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles
title Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles
title_full Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles
title_fullStr Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles
title_full_unstemmed Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles
title_short Constitutive Gene Expression in Monocytes from Chronic HIV-1 Infection Overlaps with Acute Toll-Like Receptor Induced Monocyte Activation Profiles
title_sort constitutive gene expression in monocytes from chronic hiv-1 infection overlaps with acute toll-like receptor induced monocyte activation profiles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399809/
https://www.ncbi.nlm.nih.gov/pubmed/22815948
http://dx.doi.org/10.1371/journal.pone.0041153
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