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. Author manuscript; available in PMC: 2018 Mar 1.
Published in final edited form as: Radiat Res. 2017 Feb 22;187(3):367–381. doi: 10.1667/RR14623.1

Fig. 7.

Fig. 7

Measurement of extracellular TGF-β1. Conditioned media from PBS- or 30 μM MnTE-2-PyP (T2E)-treated wild-type mouse prostate fibroblasts and NOX4−/− mouse prostate fibroblasts were subjected to an activated TGF-β1 ELISA after activation of extracellular TGF-β1 by acidification. The data represent a fold change value of raw absorbance at 450 nm (subtracted by absorbance value at 540 nm). Data represent the mean ± standard deviation and were obtained from three independent experiments. The differences of mean absorbance were analyzed for significance using one-way ANOVA followed by post hoc Holm-Sidak correction for multiple comparisons. *Significant difference compared to wild-type nonirradiated fibroblasts; #significant difference compared to wild-type 2 Gy irradiated fibroblasts; $significant difference compared to T2E-treated nonirradiated fibroblasts; and %significant difference compared to T2E-treated 2 Gy irradiated fibroblasts.