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NFκB and HIF display synergistic behaviour during hypoxic inflammation
by
Birtwistle, Marc
, Bruning, Ulrike
, Frank, Till
, Fitzpatrick, Susan F.
, Taylor, Cormac T.
, Cheong, Alex
in
Animals
/ Base Sequence
/ Binding sites
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell culture
/ Cell Line
/ Cell Line, Tumor
/ Cellular biology
/ Copepoda - enzymology
/ Culture media
/ Cyclooxygenase 2 - genetics
/ Cyclooxygenase-2
/ Cytokines
/ Gene expression
/ Gene regulation
/ Genes, Reporter
/ Humans
/ Hypoxia
/ Hypoxia - genetics
/ Hypoxia - immunology
/ Hypoxia-Inducible Factor 1 - genetics
/ Hypoxia-Inducible Factor 1 - immunology
/ Inflammation
/ Inflammation - genetics
/ Inflammation - immunology
/ Life Sciences
/ Luciferases - genetics
/ Mathematical models
/ Models, Biological
/ Molecular Sequence Data
/ NF-kappa B - genetics
/ NF-kappa B - immunology
/ NF-κB protein
/ Promoter Regions, Genetic
/ Proteins
/ Regulatory sequences
/ Research Article
/ Signal transduction
/ Transcription factors
/ Transcription, Genetic
2012
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NFκB and HIF display synergistic behaviour during hypoxic inflammation
by
Birtwistle, Marc
, Bruning, Ulrike
, Frank, Till
, Fitzpatrick, Susan F.
, Taylor, Cormac T.
, Cheong, Alex
in
Animals
/ Base Sequence
/ Binding sites
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell culture
/ Cell Line
/ Cell Line, Tumor
/ Cellular biology
/ Copepoda - enzymology
/ Culture media
/ Cyclooxygenase 2 - genetics
/ Cyclooxygenase-2
/ Cytokines
/ Gene expression
/ Gene regulation
/ Genes, Reporter
/ Humans
/ Hypoxia
/ Hypoxia - genetics
/ Hypoxia - immunology
/ Hypoxia-Inducible Factor 1 - genetics
/ Hypoxia-Inducible Factor 1 - immunology
/ Inflammation
/ Inflammation - genetics
/ Inflammation - immunology
/ Life Sciences
/ Luciferases - genetics
/ Mathematical models
/ Models, Biological
/ Molecular Sequence Data
/ NF-kappa B - genetics
/ NF-kappa B - immunology
/ NF-κB protein
/ Promoter Regions, Genetic
/ Proteins
/ Regulatory sequences
/ Research Article
/ Signal transduction
/ Transcription factors
/ Transcription, Genetic
2012
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NFκB and HIF display synergistic behaviour during hypoxic inflammation
by
Birtwistle, Marc
, Bruning, Ulrike
, Frank, Till
, Fitzpatrick, Susan F.
, Taylor, Cormac T.
, Cheong, Alex
in
Animals
/ Base Sequence
/ Binding sites
/ Biochemistry
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Cell culture
/ Cell Line
/ Cell Line, Tumor
/ Cellular biology
/ Copepoda - enzymology
/ Culture media
/ Cyclooxygenase 2 - genetics
/ Cyclooxygenase-2
/ Cytokines
/ Gene expression
/ Gene regulation
/ Genes, Reporter
/ Humans
/ Hypoxia
/ Hypoxia - genetics
/ Hypoxia - immunology
/ Hypoxia-Inducible Factor 1 - genetics
/ Hypoxia-Inducible Factor 1 - immunology
/ Inflammation
/ Inflammation - genetics
/ Inflammation - immunology
/ Life Sciences
/ Luciferases - genetics
/ Mathematical models
/ Models, Biological
/ Molecular Sequence Data
/ NF-kappa B - genetics
/ NF-kappa B - immunology
/ NF-κB protein
/ Promoter Regions, Genetic
/ Proteins
/ Regulatory sequences
/ Research Article
/ Signal transduction
/ Transcription factors
/ Transcription, Genetic
2012
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NFκB and HIF display synergistic behaviour during hypoxic inflammation
Journal Article
NFκB and HIF display synergistic behaviour during hypoxic inflammation
2012
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Overview
The oxygen-sensitive transcription factor hypoxia inducible factor (HIF) is a key regulator of gene expression during adaptation to hypoxia. Crucially, inflamed tissue often displays regions of prominent hypoxia. Recent studies have shown HIF signalling is intricately linked to that of the pro-inflammatory transcription factor nuclear factor kappa B (NFκB) during hypoxic inflammation. We describe the relative temporal contributions of each to hypoxia-induced inflammatory gene expression and investigate the level of crosstalk between the two pathways using a novel
Gaussia princeps
luciferase (Gluc) reporter system. Under the control of an active promoter, Gluc is expressed and secreted into the cell culture media, where it can be sampled and measured over time. Thus, Gluc constructs under the control of either HIF or NFκB were used to resolve their temporal transcriptional dynamics in response to hypoxia and to cytokine stimuli, respectively. We also investigated the interactions between HIF and NFκB activities using a construct containing the sequence from the promoter of the inflammatory gene cyclooxygenase 2 (COX-2), which includes functionally active binding sites for both HIF and NFκB. Finally, based on our experimental data, we constructed a mathematical model of the binding affinities of HIF and NFκB to their respective response elements to analyse transcriptional crosstalk. Taken together, these data reveal distinct temporal HIF and NFκB transcriptional activities in response to hypoxic inflammation. Furthermore, we demonstrate synergistic activity between these two transcription factors on the regulation of the COX-2 promoter, implicating a co-ordinated role for both HIF and NFκB in the expression of COX-2 in hypoxic inflammation.
Publisher
SP Birkhäuser Verlag Basel,Springer Nature B.V
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