Research Paper Volume 16, Issue 19 pp 12697—12725

A new model and precious tool to study molecular mechanisms of macrophage aging

class="figure-viewer-img"

Figure 6. CB3 effects on proliferation and apoptosis in aged macrophages in vitro. Macrophages are chronically treated with 100uM CB3 for up to 14 days. (A) RT-qPCR analysis for p21CIP1 transcripts normalized to 36B4 (n=7). (B) Immunoblot and p21CIP1 quantification by densitometric analysis (n=3). (C) Quantification of EdU-positive cells. EdU was added for 24 h before analysis. (D) Quantification of TUNEL positive cells (n=3). Error bars represent the mean ± SEM. p-values were obtained comparing groups overtime using a non-parametric one-way ANOVA analysis (Kruskal-Wallis analysis followed by Dunnett’s multiple comparison test; *p<0.05; ***p<0.001) or using a non-parametric t-test (Mann-Whitney) to analyze the significance between groups treated or not treated with CB3 (#p<0.05).