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. 2013 Feb 20;304(8):C768–C779. doi: 10.1152/ajpcell.00417.2012

Fig. 6.

Fig. 6.

Restoration of 64Cu uptake copper uptake in BSO- inhibited cells with GSH supplementation. A: cells were incubated for 48 h in media without or with 500 μM BSO (1st 2 bars) followed by overnight treatment with 1.5 mM GSH diethyl ester, a membrane permeable form of GSH which is hydrolyzed to release GSH in the cytoplasm (3rd and 4th bars) before 64Cu uptake assay. B: 64Cu uptake copper uptake and cellular GSH levels in cells treated with BSO or BSO and 1.5 or 4.0 mM GSHEt2 (GSH). Controls (100%) are cells with no treatments. C: BSO effect on copper uptake in other cell lines expressing only endogenous CTR1. Cells were incubated for 48 h in medium with or without 500 μM BSO or with BSO treatment and overnight incubation in 1.5 mM GSHEt2. Because GSHEt2 was toxic to rat smooth muscle cells, no results are shown for those cells. * P < 0.05, significantly different value vs. control by Student's t-test, unpaired.

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