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Journal: Molecular Biomedicine
Article Title: Lipid nanoparticle-mediated transcription factor EB mRNA delivery for the treatment of metabolic dysfunction-associated steatotic liver disease
doi: 10.1186/s43556-026-00615-0
Figure Lengend Snippet: LNP-TFEB and S211A enhanced autophagy and promoted lipid metabolism in the mouse liver. a Representative Western blot images and b corresponding quantitative analysis of TFEB (TFEB and FLAG-tag detection confirmed LNP-mediated expression of TFEB and S211A), autophagy-related proteins (LC3, P62), lipid metabolism-related proteins (PPARα, ATGL, CPT1A) and lipid synthesis-related proteins (FASN, ACC, SREBP1) in mouse liver ( n = 4 or 6 per group). c Relative hepatic mRNA expression levels of autophagy-related genes, lipid catabolism-related genes and lipid synthesis and transport-related genes, as determined by qPCR ( n = 5 or 6 per group). d Representative hematoxylin and eosin (H&E) staining images of liver sections and the corresponding NAFLD activity score (NAS) ( n = 6 per group). e Representative images of Sirius Red staining and quantification of the relative fibrotic area ( n = 6 per group). f Representative BODIPY fluorescence staining images of neutral lipids in liver sections and quantification of fluorescence intensity. cv: Central vein ( n = 6 per group). g Representative F4/80 immunofluorescence staining images showing macrophage infiltration and the corresponding quantitative analysis ( n = 5 per group). Scale bar = 100 μm. Data are expressed as mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001
Article Snippet: The membranes were blocked with 5% skim milk for 2 h and then incubated overnight at 4 °C with the following primary antibodies: anti-TFEB (1:1,000, Bethyl, A303-673A), anti-LC3 (1:1,000, Abclonal, A15591),
Techniques: Western Blot, Analysis, FLAG-tag, Expressing, Staining, Activity Assay, Fluorescence, Immunofluorescence