author_facet Schmelzer, Constance
Döring, Frank
Schmelzer, Constance
Döring, Frank
author Schmelzer, Constance
Döring, Frank
spellingShingle Schmelzer, Constance
Döring, Frank
BioFactors
Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
Clinical Biochemistry
Molecular Medicine
General Medicine
Biochemistry
author_sort schmelzer, constance
spelling Schmelzer, Constance Döring, Frank 0951-6433 1872-8081 Wiley Clinical Biochemistry Molecular Medicine General Medicine Biochemistry http://dx.doi.org/10.1002/biof.93 <jats:title>Abstract</jats:title><jats:p>Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub>) is an obligatory element in the respiratory chain and functions as a potent antioxidant of lipid membranes. More recently, anti‐inflammatory effects as well as an impact of CoQ<jats:sub>10</jats:sub> on gene expression have been observed. To reveal putative effects of Q<jats:sub>10</jats:sub> on LPS‐induced gene expression, whole genome expression analysis was performed in the monocytic cell line THP‐1. Thousand one hundred twenty‐nine and 710 probe sets have been identified to be significantly (<jats:italic>P</jats:italic> ≤ 0.05) up and downregulated in LPS‐treated cells when compared with controls, respectively. Text mining analysis of the top 50 LPS upregulated genes revealed a functional connection in the NFκB pathway and confirmed our applied <jats:italic>in vitro</jats:italic> stimulation model. Moreover, 33 LPS‐sensitive genes have been identified to be significantly downregulated by Q<jats:sub>10</jats:sub>‐treatment between a factor of 1.32 and 1.85. GeneOntology (GO) analysis revealed for the Q<jats:sub>10</jats:sub>‐sensitve genes a primary involvement in protein metabolism (<jats:italic>e.g.</jats:italic>, HERC1 and EPS15), cell proliferation (<jats:italic>e.g.</jats:italic>, CCDC100 and SMURF1), and transcriptional processes (<jats:italic>e.g.</jats:italic>, CNOT4 and STK4). Three genes were either related to NFκB transcription factor activity (ERC1), cytokinesis (DIAPH2), or modulation of oxidative stress (MSRA). In conclusion, our data provide evidence that Q<jats:sub>10</jats:sub> downregulates LPS‐inducible genes in the monocytic cell line THP‐1. Thus, the previously described effects of Q<jats:sub>10</jats:sub> on the reduction of proinflammatory mediators might be due to its antioxidant impact on gene expression.</jats:p> Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes BioFactors
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title Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_unstemmed Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_full Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_fullStr Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_full_unstemmed Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_short Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_sort identification of lps‐inducible genes downregulated by ubiquinone in human thp‐1 monocytes
topic Clinical Biochemistry
Molecular Medicine
General Medicine
Biochemistry
url http://dx.doi.org/10.1002/biof.93
publishDate 2010
physical 222-228
description <jats:title>Abstract</jats:title><jats:p>Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub>) is an obligatory element in the respiratory chain and functions as a potent antioxidant of lipid membranes. More recently, anti‐inflammatory effects as well as an impact of CoQ<jats:sub>10</jats:sub> on gene expression have been observed. To reveal putative effects of Q<jats:sub>10</jats:sub> on LPS‐induced gene expression, whole genome expression analysis was performed in the monocytic cell line THP‐1. Thousand one hundred twenty‐nine and 710 probe sets have been identified to be significantly (<jats:italic>P</jats:italic> ≤ 0.05) up and downregulated in LPS‐treated cells when compared with controls, respectively. Text mining analysis of the top 50 LPS upregulated genes revealed a functional connection in the NFκB pathway and confirmed our applied <jats:italic>in vitro</jats:italic> stimulation model. Moreover, 33 LPS‐sensitive genes have been identified to be significantly downregulated by Q<jats:sub>10</jats:sub>‐treatment between a factor of 1.32 and 1.85. GeneOntology (GO) analysis revealed for the Q<jats:sub>10</jats:sub>‐sensitve genes a primary involvement in protein metabolism (<jats:italic>e.g.</jats:italic>, HERC1 and EPS15), cell proliferation (<jats:italic>e.g.</jats:italic>, CCDC100 and SMURF1), and transcriptional processes (<jats:italic>e.g.</jats:italic>, CNOT4 and STK4). Three genes were either related to NFκB transcription factor activity (ERC1), cytokinesis (DIAPH2), or modulation of oxidative stress (MSRA). In conclusion, our data provide evidence that Q<jats:sub>10</jats:sub> downregulates LPS‐inducible genes in the monocytic cell line THP‐1. Thus, the previously described effects of Q<jats:sub>10</jats:sub> on the reduction of proinflammatory mediators might be due to its antioxidant impact on gene expression.</jats:p>
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author Schmelzer, Constance, Döring, Frank
author_facet Schmelzer, Constance, Döring, Frank, Schmelzer, Constance, Döring, Frank
author_sort schmelzer, constance
container_issue 3
container_start_page 222
container_title BioFactors
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description <jats:title>Abstract</jats:title><jats:p>Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub>) is an obligatory element in the respiratory chain and functions as a potent antioxidant of lipid membranes. More recently, anti‐inflammatory effects as well as an impact of CoQ<jats:sub>10</jats:sub> on gene expression have been observed. To reveal putative effects of Q<jats:sub>10</jats:sub> on LPS‐induced gene expression, whole genome expression analysis was performed in the monocytic cell line THP‐1. Thousand one hundred twenty‐nine and 710 probe sets have been identified to be significantly (<jats:italic>P</jats:italic> ≤ 0.05) up and downregulated in LPS‐treated cells when compared with controls, respectively. Text mining analysis of the top 50 LPS upregulated genes revealed a functional connection in the NFκB pathway and confirmed our applied <jats:italic>in vitro</jats:italic> stimulation model. Moreover, 33 LPS‐sensitive genes have been identified to be significantly downregulated by Q<jats:sub>10</jats:sub>‐treatment between a factor of 1.32 and 1.85. GeneOntology (GO) analysis revealed for the Q<jats:sub>10</jats:sub>‐sensitve genes a primary involvement in protein metabolism (<jats:italic>e.g.</jats:italic>, HERC1 and EPS15), cell proliferation (<jats:italic>e.g.</jats:italic>, CCDC100 and SMURF1), and transcriptional processes (<jats:italic>e.g.</jats:italic>, CNOT4 and STK4). Three genes were either related to NFκB transcription factor activity (ERC1), cytokinesis (DIAPH2), or modulation of oxidative stress (MSRA). In conclusion, our data provide evidence that Q<jats:sub>10</jats:sub> downregulates LPS‐inducible genes in the monocytic cell line THP‐1. Thus, the previously described effects of Q<jats:sub>10</jats:sub> on the reduction of proinflammatory mediators might be due to its antioxidant impact on gene expression.</jats:p>
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spelling Schmelzer, Constance Döring, Frank 0951-6433 1872-8081 Wiley Clinical Biochemistry Molecular Medicine General Medicine Biochemistry http://dx.doi.org/10.1002/biof.93 <jats:title>Abstract</jats:title><jats:p>Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub>) is an obligatory element in the respiratory chain and functions as a potent antioxidant of lipid membranes. More recently, anti‐inflammatory effects as well as an impact of CoQ<jats:sub>10</jats:sub> on gene expression have been observed. To reveal putative effects of Q<jats:sub>10</jats:sub> on LPS‐induced gene expression, whole genome expression analysis was performed in the monocytic cell line THP‐1. Thousand one hundred twenty‐nine and 710 probe sets have been identified to be significantly (<jats:italic>P</jats:italic> ≤ 0.05) up and downregulated in LPS‐treated cells when compared with controls, respectively. Text mining analysis of the top 50 LPS upregulated genes revealed a functional connection in the NFκB pathway and confirmed our applied <jats:italic>in vitro</jats:italic> stimulation model. Moreover, 33 LPS‐sensitive genes have been identified to be significantly downregulated by Q<jats:sub>10</jats:sub>‐treatment between a factor of 1.32 and 1.85. GeneOntology (GO) analysis revealed for the Q<jats:sub>10</jats:sub>‐sensitve genes a primary involvement in protein metabolism (<jats:italic>e.g.</jats:italic>, HERC1 and EPS15), cell proliferation (<jats:italic>e.g.</jats:italic>, CCDC100 and SMURF1), and transcriptional processes (<jats:italic>e.g.</jats:italic>, CNOT4 and STK4). Three genes were either related to NFκB transcription factor activity (ERC1), cytokinesis (DIAPH2), or modulation of oxidative stress (MSRA). In conclusion, our data provide evidence that Q<jats:sub>10</jats:sub> downregulates LPS‐inducible genes in the monocytic cell line THP‐1. Thus, the previously described effects of Q<jats:sub>10</jats:sub> on the reduction of proinflammatory mediators might be due to its antioxidant impact on gene expression.</jats:p> Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes BioFactors
spellingShingle Schmelzer, Constance, Döring, Frank, BioFactors, Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes, Clinical Biochemistry, Molecular Medicine, General Medicine, Biochemistry
title Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_full Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_fullStr Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_full_unstemmed Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_short Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
title_sort identification of lps‐inducible genes downregulated by ubiquinone in human thp‐1 monocytes
title_unstemmed Identification of LPS‐inducible genes downregulated by ubiquinone in human THP‐1 monocytes
topic Clinical Biochemistry, Molecular Medicine, General Medicine, Biochemistry
url http://dx.doi.org/10.1002/biof.93