Modulation of the Receptor Tyrosine Kinase TIE2/Tek Pathway by NRF2 Activation in Neurovascular Endothelial Cells.
First-pass extracted concept
TIE2/Tek pathway
Candidate: concept label1 source documents4 linked claims
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Aliases
TEK, Tie2
Evidence Snippets
Supporting Sources
Linked Claims
NRF2 activation downregulates TIE2/Tek expression in mouse neuroendothelial cells.
Quoted textsource-backed
Among these, the TIE2/Tek receptor, essential for vascular development and integrity, was downregulated upon NRF2 activation
TIE2/Tek repression after NRF2 activation is independent of the NRF2 repressor BACH1.
Quoted textsource-backed
Hemin treatment and knockdown revealed that TIE2/Tek repression is independent of the NRF2 repressor BACH1.
Available mRNA stability and ChIP analyses do not support post-transcriptional or direct transcriptional repression of TIE2/Tek by NRF2.
Quoted textsource-backed
mRNA stability and ChIP analyses indicated no post-transcriptional or direct transcriptional repression by NRF2.
The findings suggest an alternative NRF2-dependent mechanism affects TIE2/Tek levels and may influence angiogenic regulation.
Quoted textsource-backed
These findings suggest an alternative NRF2-dependent mechanism affecting TIE2/Tek levels and potentially influencing angiogenic regulation.