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. Author manuscript; available in PMC: 2010 Dec 1.
Published in final edited form as: J Dermatol Sci. 2009 Nov 10;56(3):154–162. doi: 10.1016/j.jdermsci.2009.08.008

Figure 6. T-oligo protects fibroblasts from oxidative damage.

Figure 6

Newborn fibroblasts were processed as per Materials and Methods, and cells were then treated with 25 μM fresh H2O2 or diluent for one hour and then provided fresh medium without T-oligos. Cell yields were determined 8, 16, 24 and 48 hours later. Fibroblasts pretreated with T-oligo and then diluent proliferated more slowly than diluent pretreated cells (p< 0.0001), as expected, given the initial T-oligo induced S-phase arrest[13], but both showed exponential growth after the first 24 hours. Interestingly, fibroblasts pretreated with T-oligo and then challenged with H2O2 proliferated significantly better than diluent pretreated H2O2-challenged fibroblasts (p< 0.006). Data points are the mean ± SEM for 3 separate experiments with different donor cells.