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. Author manuscript; available in PMC: 2015 Nov 20.
Published in final edited form as: Sci Transl Med. 2015 May 20;7(288):288ra79. doi: 10.1126/scitranslmed.aaa5094

Fig. 4. Reduced pSmad3 in mice treated with c8.

Fig. 4

(A) Representative liver (top panels) and lung (bottom panels) sections from mice treated with c16 or c8 after induced fibrotic injury stained for fibroblasts [PDGFRβ (plateletderived growth factor receptor β), green] and pSmad3 (red). (B) Quantification of pSmad3 nuclear intensity within individual PDGFRβ+ cells documents a significant reduction in fibroblast-specific pSmad3 in fibrotic mice treated with c8. Data represent means ± SEM; n = 102 (Bleo c8), n = 254 (Bleo c16), n = 262 (CCl4 c8), and n = 361(CCl4 c16). For both comparisons, P < 0.0001 (shown is a representative example of the distribution of individual pSmad3 mean fluorescence intensities in PDGFRβ+ cells, and the average of these means, for a single sample condition). Scale bar, 100 µm. P values were calculated using the unpaired Student’s t tests.