BioMed Research International · 2016 · 73 citations · 18 references
Life SciencesBiochemistryPlant SciencesCell SignalingPlant BiochemistryRedox BiochemistryAntioxidant DefenseGlutathione MetabolismOxidative StressOxidative Stress MechanismsReactive Oxygen SpeciesRedox SignalingCellular Antioxidant DefenseConstitutive Gene ExpressionGlutathione S-transferase ActivityNrf2 Pathway ActivationNrf2 Signaling PathwayNrf2-mediated ResponsesNuclear Factor Erythroid 2-Related Factor 2 SignalingWestern Blot Analysis
Quercetin and phenylpropanoids are well known chemoprotective compounds identified in many plants. This study was aimed at determining their effects on activation of Nuclear factor erythroid 2-related factor 2 (Nrf2) antioxidant response element (Nrf2-ARE) signalling pathway and expression of its important downstream effector phase II detoxification enzyme glutathione-S-transferase P1 (GSTP1) in BJ foreskin fibroblasts and skin HaCaT keratinocytes. Cell lines and their corresponding Nrf2-ARE luciferase reporter cells were treated by ginger phenylpropanoids and quercetin for 10 h and the level of Nrf2 activity was subsequently determined. Both, ginger phenylpropanoids and quercetin, significantly increased the level of Nrf2 activity. Subsequent western blot analyses of proteins showed the increased expression level of glutathione-S-transferase P1 (GSTP1) in BJ cells but not in HaCaT cells. Such phenomenon of unresponsive downstream target expression in HaCaT cells was consistent with previous studies showing a constitutive expression of their GSTP1. Thus, while both ginger phenylpropanoids and quercetin have the property of increasing the level of Nrf2 both in HaCaT and in BJ cells, their effects on its downstream signalling were mediated only in BJ cells.
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Regulation of JNK signaling by GSTp
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Human glutathione S-transferase P1-1 interacts with TRAF2 and regulates TRAF2–ASK1 signals
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