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HIF2α-dependent Dock4/Rac1-signaling regulates formation of adherens junctions and cell polarity in normoxia.

I RaykhelV-P RonkainenJohanna MyllyharjuAki Manninen
Published in: Scientific reports (2024)
Hypoxia-inducible factors (HIF) 1 and 2 regulate similar but distinct sets of target genes. Although HIFs are best known for their roles in mediating the hypoxia response accumulating evidence suggests that under certain conditions HIFs, particularly HIF2, may function also under normoxic conditions. Here we report that HIF2α functions under normoxic conditions in kidney epithelial cells to regulate formation of adherens junctions. HIF2α expression was required to induce Dock4/Rac1/Pak1-signaling mediating stability and compaction of E-cadherin at nascent adherens junctions. Impaired adherens junction formation in HIF2α- or Dock4-deficient cells led to aberrant cyst morphogenesis in 3D kidney epithelial cell cultures. Taken together, we show that HIF2α functions in normoxia to regulate epithelial morphogenesis.
Keyphrases
  • endothelial cells
  • single molecule
  • poor prognosis
  • induced apoptosis
  • oxidative stress
  • gene expression
  • cell death
  • mesenchymal stem cells
  • genome wide
  • dna methylation
  • signaling pathway
  • bone marrow
  • binding protein