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. 2020 Sep 18;10:1780. doi: 10.3389/fonc.2020.01780

Figure 1.

Figure 1

The Toll-like receptor 3 (TLR3) ligand induces cell proliferation and is stunted by myeloid differentiation primary response 88 (MyD88) inhibitor. Breast cancer cells were pretreated with MyD88 inhibitor (1 μM) 4 h prior to the addition of the TLR3 ligand (10 μg/ml) for 24 h before cells were counted. Control indicates cells were not treated with TLR3 ligand or MyD88 inhibitor. Growth kinetic assay. (A) T47D and (B) MDA-MB-231 showing proliferative effect of TLR3 ligand. Inhibition of MyD88 dimerization restrict the proliferative effect. (C) Contour plots for BrdU-cell proliferation assay using T47D cells. Cells were pretreated with MyD88 inhibitor (1 μM) 4 h prior to addition TLR3 ligand (10 μg/ml) for 24 h before labeling with BrdU and detecting by flow cytometry. Contour plots of DNA-7AAD-A vs. log BrdU-FITC showing G0/G1, S, and G2/M gates of control cells, cells treated with TLR3 ligand, cells treated with TLR3 ligand and MyD88 inhibitor, and cells treated with only MyD88 inhibitor. (D) Bar graph showing percentage of S-phase-gated cells among the different experimental cell groups following BrdU incorporation. The results are presented as mean ± SD, and p < 0.05 is treated as significant.