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. Author manuscript; available in PMC: 2014 Mar 1.
Published in final edited form as: J Mol Neurosci. 2012 Oct 15;49(3):507–511. doi: 10.1007/s12031-012-9904-4

Fig. 1.

Fig. 1

Quantification of neuronal thiol oxidation as an indicator of neuronal oxidative stress. a–c The false-colored images represent SS/SH ratios assessed in MAP2+ neurons by confocal microscopy. High ratios (white-yellow) indicate high levels of neuronal thiol oxidation, whereas low ratios (blue-green) indicate low levels of neuronal thiol oxidation. Each image is from a neuron-astrocyte co-culture treated with 20 nM rotenone for 24 h. The DJ-1 expression status of each co-cultured astrocyte type is indicated below the figure. d–f MAP2+ (blue fluorescence) neuronal cell fields that correspond to the thiol oxidation images in a–c, respectively (boxes indicate the portions shown in the upper images). g Representative neuron-astrocyte co-culture showing the relative densities of each cell type at the time of assessments