Figure - available from: Current Molecular Pharmacology
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Relationship between DDR1 repression and CCL4-induced liver fibrosis. Mouse liver tissue stained with (A) H&E, (B) Masson, and (E) DDR1; n = 6. Original magnification: ×100. (C) Quantification of Masson-positive areas in liver sections. (F) Quantification of immunostained areas in liver sections. (G) Representative immunoblot and quantification of DDR1 protein levels; n = 4. β-Tubulin was used as a loading control. (H) Gene expression of DDR1 in mouse livers via RT-qPCR; n = 3. (D) Relative ALT and AST activities in serum from WT and DDR1-KO mice after being treated with CCl4; n = 6. Data are expressed as mean ± standard deviation. *P <0.05, **P <0.01, and ***P <0.001.
Source publication
Background
This study investigated the role and potential mechanisms of Discoidin domain receptors-1 (DDR1) during liver fibrogenesis.
Methods
Blood and livers were collected from mice. In the in vitro experiments, human normal hepatocyte (LO2 cell line) and human hepatoma cells (HepG2 cell line) with overexpressed DDR1 (DDR1-OE) or DDR1 knockdown...