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. 2017 Oct 24;243(1):1–12. doi: 10.1177/1535370217738730

Figure 4.

Figure 4.

Increased hepatic inflammation during progression of NAFLD. (a) Intravital microscopic analysis of the number of adherent leukocytes in postsinusoidal venules of healthy livers (control) and livers of STZ/HFD-treated mice at ages of 6, 8, 12, and 20 weeks. Values are given as mean±s.e.m. (control: n=9, 6 weeks: n=10, 8 weeks: n=10, 12 weeks: n=10, 20 weeks: n=11). Significance of differences between the groups was tested by one-way ANOVA (Bonferroni t-test), *P<0.05 vs. control. (b) Quantitative analysis of CAE-positive cells in liver sections of STZ/HFD-treated mice (6, 8, 12, and 20 weeks). Data are presented as box plots indicating the median, the interquartile range in form of a box, and the minimum and maximum as whiskers (6 weeks: n=7, 8 weeks: n=7, 12 weeks: n=9, 20 weeks: n=7). (c) Upper panel: Representative in vivo images of the liver of a control and a 20 weeks old STZ/HFD-treated mouse showing numerous leukocytes (arrows) adhering at the endothelium of the venule in the diseased liver (12 weeks) (400× magnification). Lower panel: The images depict representative HPF of CAE-stained liver tissue of 6 and 12 weeks old mice with red stained granulocytes (arrows). (d) Intravital microscopic analysis of sinusoidal leukostasis of healthy livers (control) and livers of STZ/HFD-treated mice at ages of 6, 8, 12, and 20 weeks. Values are given as mean±s.e.m. (control: n=11, 6 weeks: n=10, 8 weeks: n=10, 12 weeks: n=10, 20 weeks: n=10). (A color version of this figure is available in the online journal.)

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