Vascular endothelial growth factor on Runt‐related transcript factor‐2 in aortic valve cells

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Abstract
Background: Calcific aortic valve disease is associated with ageing and high mortality. However, no effective pharmacological treatment has been developed. Vascular endothelial growth factor (VEGF) and its receptor are overexpressed in the calcified aortic valve tissue. However, the role of VEGF in calcific aortic valve disease pathogenesis and its underlying mechanisms remain unclear. Materials and methods: Runt‐related transcription factor 2 expression and calcium‐related signalling were investigated in porcine valvular interstitial cells with or without human VEGF‐A recombinant protein (VEGF 165 , 1‐100 ng/mL) treatment and/or calmodulin‐dependent kinase II (CaMKII) inhibitor (KN93, 10 µmol/L) and inositol triphosphate receptor inhibitor (2‐aminoethyldiphenyl borate, 30 µmol/L) for 5 days. Results: VEGF 165 ‐treated cells had higher Runt‐related transcription factor 2 expression and CaMKII/ adenosine 3',5'‐monophosphate response element‐binding protein (CREB) signalling activation than did control cells. KN93 reduced Runt‐related transcription factor 2 expression and CREB phosphorylation in VEGF 165 ‐treated cells. The 2‐aminoethyldiphenyl borate also reduced Runt‐related transcription factor 2 expression in VICs treated with VEGF 165 . Conclusion: VEGF upregulated Runt‐related transcription factor 2 expression in VICs by activating the IP3R/CaMKII/CREB signalling pathway.
Funding Information
  • Taipei Medical University (TMU109‐AE1‐B09)
  • Ministry of Science and Technology, Taiwan (MOST106‐2221‐E030‐011‐MY2)
  • Ministry of Science and Technology, Taiwan (MOST106‐2221‐E030‐012)
  • Ministry of Science and Technology, Taiwan (MOST108‐2314‐B‐038‐120)

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