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Sökning: onr:"swepub:oai:lup.lub.lu.se:24d7cb43-edeb-454b-a183-6552fa5fbe8a" > GFAT1 phosphorylati...

  • Zibrova, DaryaUniversitätsklinikum Jena (författare)

GFAT1 phosphorylation by AMPK promotes VEGF-induced angiogenesis

  • Artikel/kapitelEngelska2017

Förlag, utgivningsår, omfång ...

  • 2017
  • 19 s.

Nummerbeteckningar

  • LIBRIS-ID:oai:lup.lub.lu.se:24d7cb43-edeb-454b-a183-6552fa5fbe8a
  • https://lup.lub.lu.se/record/24d7cb43-edeb-454b-a183-6552fa5fbe8aURI
  • https://doi.org/10.1042/BCJ20160980DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:art swepub-publicationtype
  • Ämneskategori:ref swepub-contenttype

Anmärkningar

  • Activation of AMP-activated protein kinase (AMPK) in endothelial cells regulates energy homeostasis, stress protection and angiogenesis, but the underlying mechanisms are incompletely understood. Using a label-free phosphoproteomic analysis, we identified glutamine:fructose-6-phosphate amidotransferase 1 (GFAT1) as an AMPK substrate. GFAT1 is the rate-limiting enzyme in the hexosamine biosynthesis pathway (HBP) and as such controls the modification of proteins by O-linked β-N-acetylglucosamine (O-GlcNAc). In the present study, we tested the hypothesis that AMPK controls O-GlcNAc levels and function of endothelial cells via GFAT1 phosphorylation using biochemical, pharmacological, genetic and in vitro angiogenesis approaches. Activation of AMPK in primary human endothelial cells by 5-aminoimidazole-4-carboxamide riboside (AICAR) or by vascular endothelial growth factor (VEGF) led to GFAT1 phosphorylation at serine 243. This effect was not seen when AMPK was down-regulated by siRNA. Upon AMPK activation, diminished GFAT activity and reduced O-GlcNAc levels were observed in endothelial cells containing wild-type (WT)-GFAT1 but not in cells expressing non-phosphorylatable S243A-GFAT1. Pharmacological inhibition or siRNA-mediated down-regulation of GFAT1 potentiated VEGF-induced sprouting, indicating that GFAT1 acts as a negative regulator of angiogenesis. In cells expressing S243A-GFAT1, VEGF-induced sprouting was reduced, suggesting that VEGF relieves the inhibitory action of GFAT1/HBP on angiogenesis via AMPK-mediated GFAT1 phosphorylation. Activation of GFAT1/HBP by high glucose led to impairment of vascular sprouting, whereas GFAT1 inhibition improved sprouting even if glucose level was high. Our findings provide novel mechanistic insights into the role of HBP in angiogenesis. They suggest that targeting AMPK in endothelium might help to ameliorate hyperglycaemia-induced vascular dysfunction associated with metabolic disorders.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Vandermoere, FranckUniversity of Montpellier (författare)
  • Göransson, OlgaLund University,Lunds universitet,Proteinfosforylering,Forskargrupper vid Lunds universitet,Protein Phosphorylation,Lund University Research Groups(Swepub:lu)medk-ogo (författare)
  • Peggie, MarkUniversity of Dundee (författare)
  • Mariño, Karina V.Experimental Medicine and Biology Institute (IByME) (författare)
  • Knierim, AnneUniversitätsklinikum Jena (författare)
  • Spengler, KatrinUniversitätsklinikum Jena (författare)
  • Weigert, CoraGerman Center for Diabetes Research,University of Tübingen (författare)
  • Viollet, BenoitParis Descartes University,Institut Cochin (författare)
  • Morrice, Nicholas A.AB Sciex (författare)
  • Sakamoto, KeiUniversity of Dundee (författare)
  • Heller, RegineUniversitätsklinikum Jena (författare)
  • Universitätsklinikum JenaUniversity of Montpellier (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Biochemical Journal474:6, s. 983-10010264-6021

Internetlänk

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