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. 2022 May 10;20:63. doi: 10.1186/s12964-022-00871-x

Fig. 5.

Fig. 5

Matrix metalloproteases’ activity in CAFs. A Images of representative gelatin zymography gels performed on media collected from CAFs. The mean of densitometry quantification of at least three independent repetitions of gelatin zymography ± SD is shown. B As MMP14 is a membrane metalloprotease, its activity was measured in cell lysates collected from CAFs, using a fluorimetric activity assay. The data represent the mean MMP14 activity of three independent measurements ± SD. In both experiments, CAFs were obtained from fibroblasts cultured with melanoma-conditioned media (CM) or with melanoma cells on Transwell inserts (INS). Control (CTRL) constitutes of samples collected from fibroblasts cultured in a composition of FBM:DMEM (1:1 rate) medium. Asterisks indicate differences between control cells and CAFs or between different types of CAFs. The significance level was set at p ≤ 0.05 (*), p ≤ 0.01 (**) and p ≤ 0.001 (***)