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. 2017 Aug 7;7(3):624–634. doi: 10.1086/689908

Fig. 4.

Fig. 4.

BMPR2 mutation and WD have varied results on small pulmonary vessels. (a) Small pulmonary vessel density was not altered by diet or genotype. Mean vessels per 10× high power field is given (averaged over ten fields, n = 3–5 mice per bar). (b) Pulmonary vessels in mice with BMPR2 mutation showed increased medial wall thickness, but this did not vary based on diet exposure (two-way ANOVA P < 0.01 for effect of genotype, P = NS for effect of diabetogenic exposure). The mean medial wall thickness from all vessels on 15 high powered fields is given for n = 4 mice. (c) WD and mutation each significantly increased lung ROS (P < 0.01 for WD, P < 0.05 for BMPR2 mutation, n = 10–12 per bar). ROS given as fold change compared with control genotype, SD group. Comparison with SD-fed group of same genotype, *P < 0.05.