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1000 Titel
  • (H)IF applicable: promotion of neurogenesis by induced HIF-2 signalling after ischaemia
1000 Autor/in
  1. Leu, Tristan |
  2. Fandrey, Joachim |
  3. Schreiber, Timm |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-12
1000 Erschienen in
1000 Quellenangabe
  • 473(8):1287-1299
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00424-021-02600-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302505/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • HIF-2 represents a tissue-specific isoform of the hypoxia-inducible factors (HIFs) which regulate oxygen homeostasis in the cell. In acute oxygen deficiency, HIF transcription factors ensure the timely restoration of adequate oxygen supply. Particularly in medical conditions such as stroke, which have a high mortality risk due to ischaemic brain damage, rapid recovery of oxygen supply is of extraordinary importance. Nevertheless, the endogenous mechanisms are often not sufficient to respond to severe hypoxic stress with restoring oxygenation and fail to protect the tissue. Herein, we analysed murine neurospheres without functioning HIF-2α and found that special importance in the differentiation of neurons can be attributed to HIF-2 in the brain. Other processes, such as cell migration and signal transduction of different signalling pathways, appear to be mediated to some extent via HIF-2 and illustrate the function of HIF-2 in brain remodelling. Without hypoxic stress, HIF-2 in the brain presumably focuses on the fine-tuning of the neural network. However, a therapeutically increase of HIF-2 has the potential to regenerate or replace destroyed brain tissue and help minimize the consequences of an ischaemic stroke.
1000 Sacherschließung
lokal Female [MeSH]
lokal Brain
lokal Mice, Inbred C57BL [MeSH]
lokal Brain Ischemia/metabolism [MeSH]
lokal HIF-2
lokal Animals [MeSH]
lokal Mice, Knockout [MeSH]
lokal Male [MeSH]
lokal Neuroprotection [MeSH]
lokal Molecular and cellular mechanisms of disease
lokal Regeneration
lokal Neurogenesis
lokal Transcription Factors/metabolism [MeSH]
lokal Ischaemia
lokal Primary Cell Culture [MeSH]
lokal Hypoxia/metabolism [MeSH]
lokal Molecular and Cellular Mechanisms of Disease
lokal Nerve Regeneration [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TGV1LCBUcmlzdGFu|https://orcid.org/0000-0001-9585-0531|https://frl.publisso.de/adhoc/uri/U2NocmVpYmVyLCBUaW1t
1000 Hinweis
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1000 @id frl:6446942.rdf
1000 Erstellt am 2023-04-28T14:38:15.298+0200
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1000 Zuletzt bearbeitet 2023-10-20T19:17:25.960+0200
1000 Objekt bearb. Fri Oct 20 19:17:25 CEST 2023
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1000 Oai Id
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