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. 2021 Oct 29;9(11):1578. doi: 10.3390/biomedicines9111578

Figure 5.

Figure 5

(a,c) Topography AFM images of the (a) micron scale, 5 × 5 µm, and the (c) submicron, 1 × 1 µm, areas of the dehydrated CE liver ECMs of parenchymal (P) and stromal (S) origin. (b,d) Quantitative analysis of the surface roughness (b) and stiffness (d) of dehydrated LS-ECM compartments. Notably, the graph in (b) shows that the LS-ECM compartments differ by root square roughness at both the micron and submicron scales (explored in 5 × 5 µm and 1 × 1 µm images, respectively) with statistical significance. At the same time, as shown in (d), the LS-ECM compartments differ by median stiffness with a statistical significance only at the submicron scale (as explored in 1 × 1 µm images).