Journal: Molecular Medicine Reports
Article Title: Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism
doi: 10.3892/mmr.2024.13191
Figure Lengend Snippet: NF-κB inhibitor significantly inhibited the increase of Bif-1 and autophagy in J774A.1 cells. (A-D) J774A.1 cells were treated with LPS (500 ng/ml) for 6 h in the presence or absence of MLN120B (1 µM), then stimulated with 5 mM ATP for 30 min. Protein expression of (A) Bif-1, p62, LC3-II and LC3-I was investigated using western blotting. The relative protein levels of (B) Bif-1, (C) p62 and (D) LC3-II/I were analyzed using ImageJ (version 1.45; National Institutes of Health). (E) J774A.1 cell monolayers stained with LC3 (green) and DAPI (blue) fluorescence. Representative images from three independent experiments are shown. Scale bar, 10 µm (magnification, ×600). Data are expressed as mean ± SD (n=3). P<0.05 was considered to indicate a statistically significant difference (*P<0.05 vs. Con). LPS/ATP (L/A), LPS/ATP group; Con, control group treated with LPS/ATP; MLN120B, LPS/ATP group treated with MLN120B (1 µM); LPS, lipopolysaccharide; ATP, adenosine triphosphate; IL, interleukin; Bif-1, Bax-interacting factor 1; Con, control; LC, light chain; NF-κB, nuclear factor-κB.
Article Snippet: Specifically, the following inhibitors were employed: MLN120B (1 µM; Sigma-Aldrich; Merck KGaA) and MRT68921 (0.25 µM; MedChemExpress).
Techniques: Expressing, Western Blot, Staining, Fluorescence