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A. 3’-UTR of TLR2 mRNA was predicted to be targeted by miR-328-3p. B. Dual-luciferase reporter assay detects the binding of TLR2 and miR-328-3p (n = 3). C. qRT-qPCR analyzed the mRNA expression level of TLR2 in each group (n = 3). D. Western blotting analyzed the protein expression level of TLR2 in each group (n = 4). Data are presented as the mean ± SD. **P < 0.01; ***P < 0.001; ns, no significance.
