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- W2003003231 abstract "Background and aims: Severe neonatal hyperbilirubinemia can produce encephalopathy. We have previously demonstrated that exposure of SHSY5Y cells to unconjugated free bilirubin (Bf) for 24 h induces several genes as the both components of a glutamate-cystine antiporter (System Xc -). Cystine is implicated in glutathione (GSH) formation. Present study was performed to analyze if the upregulation of System excluded induced by Bf offers protection from oxidative stress. Methods: Cell viability was assessed by MTT test in SH-SY5Y cells exposed to 140 nM Bf for 24 h (T0). [14C]-cystine uptake was measured with and without l-quisqualate (an specific System Xc - inhibitor). Cells were then growth in medium for 48h (T48) and 156h (T156) in the absence of Bf. GSH level and viability were measured after H2O2 exposure. Results: Cell viability was reduced 30-40% after 24 h of Bf exposure. Cystine uptake was increased in surviving cells after 24 h Bf exposure. Further incubation with l-quisqualate for 4 h reduced cystine uptake to normal levels. GSH levels were 2.5 times that in control cell both at T0 and T48 but returned to normal levels at T156. Cells were protected from H2O2 exposure when GSH levels were high, but cells death was identical to controls at T156 when GSH levels returned to basal levels. Conclusions: SH-SY5Y cells respond to Bf exposure by an increased gene expression and activity of the System Xc -. This was associated with a higher incorporation of cystine and GSH content which protected the cell from oxidative stress H2O2 induced." @default.
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- W2003003231 date "2010-11-01" @default.
- W2003003231 modified "2023-09-25" @default.
- W2003003231 title "579 Bilirubin Upregulates Gene Expression of Slc7A11 and Increases Cystine Uptake Mediated by System Xc- in Sh-Sy5Y Neuroblastoma Cells" @default.
- W2003003231 doi "https://doi.org/10.1203/00006450-201011001-00579" @default.
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