NF‐κB and HIF crosstalk in immune responses
Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia‐inducible factors (HIFs), inflammation activates the family of transcription factor called nuclear factor‐kap...
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Published in | The FEBS journal Vol. 283; no. 3; pp. 413 - 424 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
Published by Blackwell Pub. on behalf of the Federation of European Biochemical Societies
01.02.2016
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1742-464X 1742-4658 1742-4658 |
DOI | 10.1111/febs.13578 |
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Abstract | Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia‐inducible factors (HIFs), inflammation activates the family of transcription factor called nuclear factor‐kappa B (NF‐κB). An extensive crosstalk between these two main molecular players involved in hypoxia and inflammation has been demonstrated. This crosstalk includes common activating stimuli, shared regulators and targets. In this review, we discuss the current understanding of the role of NF‐κB and HIF in the context of the immune response. We review the crosstalk between HIF and NF‐κB in the control of the immune response in different immune cell types including macrophages, neutrophils and B and T cells. Furthermore the importance of the molecular crosstalk between HIFs and NF‐κB for a variety of medical conditions will be discussed. |
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AbstractList | Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia‐inducible factors (HIFs), inflammation activates the family of transcription factor called nuclear factor‐kappa B (NF‐κB). An extensive crosstalk between these two main molecular players involved in hypoxia and inflammation has been demonstrated. This crosstalk includes common activating stimuli, shared regulators and targets. In this review, we discuss the current understanding of the role of NF‐κB and HIF in the context of the immune response. We review the crosstalk between HIF and NF‐κB in the control of the immune response in different immune cell types including macrophages, neutrophils and B and T cells. Furthermore the importance of the molecular crosstalk between HIFs and NF‐κB for a variety of medical conditions will be discussed. Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia‐inducible factors (HIFs), inflammation activates the family of transcription factor called nuclear factor‐kappa B (NF‐κB). An extensive crosstalk between these two main molecular players involved in hypoxia and inflammation has been demonstrated. This crosstalk includes common activating stimuli, shared regulators and targets. In this review, we discuss the current understanding of the role of NF‐κB and HIF in the context of the immune response. We review the crosstalk between HIF and NF‐κB in the control of the immune response in different immune cell types including macrophages, neutrophils and B and T cells. Furthermore the importance of the molecular crosstalk between HIFs and NF‐κB for a variety of medical conditions will be discussed. An intricate and complex crosstalk between HIF and NF‐κB exists in many immune cell types. The ultimate outcome is very much cell type dependent. While in certain cell types, these transcription factors cooperate, which is evident in the case of neutrophils, in other cells, they antagonise each other such as in subtypes of T cells. Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia-inducible factors (HIFs), inflammation activates the family of transcription factor called nuclear factor-kappa B (NF-κB). An extensive crosstalk between these two main molecular players involved in hypoxia and inflammation has been demonstrated. This crosstalk includes common activating stimuli, shared regulators and targets. In this review, we discuss the current understanding of the role of NF-κB and HIF in the context of the immune response. We review the crosstalk between HIF and NF-κB in the control of the immune response in different immune cell types including macrophages, neutrophils and B and T cells. Furthermore the importance of the molecular crosstalk between HIFs and NF-κB for a variety of medical conditions will be discussed.Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia-inducible factors (HIFs), inflammation activates the family of transcription factor called nuclear factor-kappa B (NF-κB). An extensive crosstalk between these two main molecular players involved in hypoxia and inflammation has been demonstrated. This crosstalk includes common activating stimuli, shared regulators and targets. In this review, we discuss the current understanding of the role of NF-κB and HIF in the context of the immune response. We review the crosstalk between HIF and NF-κB in the control of the immune response in different immune cell types including macrophages, neutrophils and B and T cells. Furthermore the importance of the molecular crosstalk between HIFs and NF-κB for a variety of medical conditions will be discussed. Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia-inducible factors (HIFs), inflammation activates the family of transcription factor called nuclear factor-kappa B (NF- Kappa B). An extensive crosstalk between these two main molecular players involved in hypoxia and inflammation has been demonstrated. This crosstalk includes common activating stimuli, shared regulators and targets. In this review, we discuss the current understanding of the role of NF- Kappa B and HIF in the context of the immune response. We review the crosstalk between HIF and NF- Kappa B in the control of the immune response in different immune cell types including macrophages, neutrophils and B and T cells. Furthermore the importance of the molecular crosstalk between HIFs and NF- Kappa B for a variety of medical conditions will be discussed. An intricate and complex crosstalk between HIF and NF- Kappa B exists in many immune cell types. The ultimate outcome is very much cell type dependent. While in certain cell types, these transcription factors cooperate, which is evident in the case of neutrophils, in other cells, they antagonise each other such as in subtypes of T cells. Hypoxia and inflammation have been associated with a number of pathological conditions, in particular inflammatory diseases. While hypoxia is mainly associated with the activation of hypoxia‐inducible factors ( HIF s), inflammation activates the family of transcription factor called nuclear factor‐kappa B ( NF ‐κB). An extensive crosstalk between these two main molecular players involved in hypoxia and inflammation has been demonstrated. This crosstalk includes common activating stimuli, shared regulators and targets. In this review, we discuss the current understanding of the role of NF ‐κB and HIF in the context of the immune response. We review the crosstalk between HIF and NF ‐κB in the control of the immune response in different immune cell types including macrophages, neutrophils and B and T cells. Furthermore the importance of the molecular crosstalk between HIF s and NF ‐κB for a variety of medical conditions will be discussed. |
Author | D'Ignazio, Laura Bandarra, Daniel Rocha, Sonia |
AuthorAffiliation | 1 Centre for Gene Regulation and Expression College of Life Sciences University of Dundee UK |
AuthorAffiliation_xml | – name: 1 Centre for Gene Regulation and Expression College of Life Sciences University of Dundee UK |
Author_xml | – sequence: 1 fullname: D'Ignazio, Laura – sequence: 2 fullname: Bandarra, Daniel – sequence: 3 fullname: Rocha, Sonia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26513405$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Animals B cells B-Lymphocyte Subsets - immunology B-Lymphocyte Subsets - metabolism HIF Humans hypoxia Hypoxia-Inducible Factor 1 - metabolism IKK immune response Immunity - immunology inflammation macrophages Macrophages - immunology Macrophages - metabolism neutrophils Neutrophils - immunology Neutrophils - metabolism NF-kappa B - metabolism NF‐κB State‐of‐the‐Art Review State‐of‐the‐Art Reviews T cells T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism T-lymphocytes transcription factor NF-kappa B |
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