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1000 Titel
  • Exposure to normobaric hypoxia shapes the acute inflammatory response in human whole blood cells in vivo
1000 Autor/in
  1. Schönberger, Tina |
  2. Jakobs, Marie |
  3. Friedel, Anna-Lena |
  4. Hörbelt-Grünheidt, Tina |
  5. Tebbe, Bastian |
  6. Witzke, Oliver |
  7. Schedlowski, Manfred |
  8. Fandrey, Joachim |
1000 Verlag Springer Berlin Heidelberg
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-05-07
1000 Erschienen in
1000 Quellenangabe
  • 476(9):1369-1381
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00424-024-02969-2 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11310243/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>Cells of the immune defence, especially leukocytes, often have to perform their function in tissue areas that are characterized by oxygen deficiency, so-called hypoxia. Physiological hypoxia significantly affects leukocyte function and controls the innate and adaptive immune response mainly through transcriptional gene regulation via the hypoxia-inducible factors (HIFs). Multiple pathogens including components of bacteria, such as lipopolysaccharides (LPS) trigger the activation of leukocytes. HIF pathway activation enables immune cells to adapt to both hypoxic environments in physiological and inflammatory settings and modulates immune cell responses through metabolism changes and crosstalk with other immune-relevant signalling pathways. To study the mutual influence of both processes in vivo, we used a human endotoxemia model, challenging participants with an intravenous LPS injection post or prior to a 4-h stay in a hypoxic chamber with normobaric hypoxia of 10.5% oxygen. We analysed changes in gene expression in whole blood cells and determined inflammatory markers to unveil the crosstalk between both processes. Our investigations showed differentially altered gene expression patterns of HIF and target genes upon in vivo treatment with LPS and hypoxia. Further, we found evidence for effects of hypoxic priming upon inflammation in combination with immunomodulatory effects in whole blood cells in vivo. Our work elucidates the complex interplay of hypoxic and inflammatory HIF regulation in human immune cells and offers new perspectives for further clinical research.</jats:p>
1000 Sacherschließung
lokal Female [MeSH]
lokal Hypoxia
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal In vivo
lokal Inflammation
lokal Endotoxemia/metabolism [MeSH]
lokal Lipopolysaccharides/pharmacology [MeSH]
lokal Oxygen/metabolism [MeSH]
lokal Whole blood cells
lokal Hypoxia/immunology [MeSH]
lokal Lipopolysaccharides/toxicity [MeSH]
lokal Endotoxemia/immunology [MeSH]
lokal Human
lokal Original Article
lokal Male [MeSH]
lokal Inflammation/metabolism [MeSH]
lokal Hypoxia/metabolism [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2Now7ZuYmVyZ2VyLCBUaW5h|https://frl.publisso.de/adhoc/uri/SmFrb2JzLCBNYXJpZQ==|https://frl.publisso.de/adhoc/uri/RnJpZWRlbCwgQW5uYS1MZW5h|https://frl.publisso.de/adhoc/uri/SMO2cmJlbHQtR3LDvG5oZWlkdCwgVGluYQ==|https://frl.publisso.de/adhoc/uri/VGViYmUsIEJhc3RpYW4=|https://frl.publisso.de/adhoc/uri/V2l0emtlLCBPbGl2ZXI=|https://frl.publisso.de/adhoc/uri/U2NoZWRsb3dza2ksIE1hbmZyZWQ=|https://frl.publisso.de/adhoc/uri/RmFuZHJleSwgSm9hY2hpbQ==
1000 Hinweis
  • DeepGreen-ID: 78dd2d71d4c742e980f7c2546c9e6749 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Deutsche Forschungsgemeinschaft |
  2. Rudolf Ackermann Stiftung |
  3. Universitätsklinikum Essen |
1000 Fördernummer
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  2. -
  3. -
1000 Förderprogramm
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  3. -
1000 Dateien
1000 Förderung
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    1000 Förderer Deutsche Forschungsgemeinschaft |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Rudolf Ackermann Stiftung |
    1000 Förderprogramm -
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer Universitätsklinikum Essen |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6519561.rdf
1000 Erstellt am 2025-07-05T18:44:13.661+0200
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1000 Zuletzt bearbeitet 2025-08-11T17:09:36.709+0200
1000 Objekt bearb. Mon Aug 11 17:09:36 CEST 2025
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1000 Oai Id
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