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. Author manuscript; available in PMC: 2016 Sep 1.
Published in final edited form as: Dev Biol. 2015 Jun 6;405(1):21–32. doi: 10.1016/j.ydbio.2015.05.024

Figure 5. Increased muscle cell proliferation in Barx1Int intestines.

Figure 5

(A-D) Fluorescence IHC of E17.5 control and mutant stomachs and intestines (n=3 each) stained simultaneously for SMA-A and DAPI (top), SMA-A and Ki67 (middle), and merged images (bottom). The border between epithelium and mesenchyme is marked with dashed lines. Scale bars, 50 μm. (E) Counts for DAPI+ and Ki67+ cells in sub-epithelial muscle (SMA+) and non-muscle (SMA) regions. Six separate areas were analyzed for each indicated tissue sample and genotype (n=3 each). Sub-epithelial composition was determined by comparing the ratio of muscle and non-muscle cells. (F) Fraction of proliferating cells, determined by counting Ki67+ cells in muscle and non-muscle compartments. Bars represent mean + SEM of biologic replicates. Comparisons were made between the same regions of the proximal intestine in wild-type and mutant mice.