Research Article

Nickel Enhances Zinc-Induced Neuronal Cell Death by Priming the Endoplasmic Reticulum Stress Response

Figure 4

GT1-7 cells (96-well culture plates at a density of cells per well) were pretreated with the indicated concentrations (mM) of carnosine just before Ni2+/Zn2+ treatment. Next, GT1-7 cells were incubated in the absence (control) or presence of NiCl2 (20 or 40 μM) and ZnCl2 (25 μM) for 24 h (a, b). GT1-7 cells (96-well culture plates at a density of cells per well) were treated with the indicated concentrations of carnosine for 24 h (c). Cell viability was determined using CellTiter-Glo® 2.0. Values represent values are described in the figure when (black: vs. control, red: vs. Zn(25)/Ni(20 or 40)).
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(b)
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