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World J Gastroenterol. Feb 14, 2014; 20(6): 1554-1564
Published online Feb 14, 2014. doi: 10.3748/wjg.v20.i6.1554
Published online Feb 14, 2014. doi: 10.3748/wjg.v20.i6.1554
Figure 2 Modulation of aspartate uptake capacity by phorbol 12-myristate 13-acetate in HepG2 cells.
A: Saturation curve for D-[3H]-aspartate uptake measured in HepG2 cells treated for 15 min with 500 nmol/L phorbol 12-myristate 13-acetate (PMA) (squares) or vehicle (circles). Data shown correspond to mean values ± SE of typical experiments performed four times in quadruplicate; B: Effect of pre-treating HepG2 cells with increasing concentrations of PMA for 15 min on D-[3H]-aspartate uptake. Data are expressed as percent of control and correspond to mean ± SE of three independent experiments performed in quadruplicate; C: modulation of D-[3H]-aspartate uptake on HepG2 cells after incubation with 500 nmol/L PMA for different periods of time. Results are expressed as percent of control (non treated cells) and correspond to means ± SE of three independent experiments performed in quadruplicate. Inset shows the data obtained after the analysis of intracellular ATP levels in HepG2 cells after treatment with 500 nmol/L PMA for 1 h. Data shown correspond to mean values ± SE of typical experiments performed four times in quadruplicate.
- Citation: Najimi M, Stéphenne X, Sempoux C, Sokal E. Regulation of hepatic EAAT-2 glutamate transporter expression in human liver cholestasis. World J Gastroenterol 2014; 20(6): 1554-1564
- URL: https://www.wjgnet.com/1007-9327/full/v20/i6/1554.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i6.1554