This section is in the Supporting Materials and is available online. Wild-type (MED1fl/fl)

and MED1ΔLiv mice were fed a high-fat diet (60% kcal fat) for 2, 4, 8, and 16 weeks. MED1fl/fl mice developed severe hepatic macrovesicular steatosis by 8 and 16 weeks on the high-fat diet but MED1ΔLiv mice exhibited only mild and spotty steatosis (Fig. 1A,B). Hepatic steatosis induced by the high-fat Venetoclax diet in MED1fl/fl mice was not associated with induction of PPARγ target gene aP2 but this protein was detected in PPARγ-induced hepatic adiposis (Fig. 1C).6 Glucose and insulin tolerance tests revealed that MED1ΔLiv mice fed a high-fat diet for 4 weeks (Supporting Fig. 1A) or 16 weeks (Supporting Fig. 1B) revealed lower glucose levels and exhibited greater insulin sensitivity (Supporting Fig. 1C) than MED1fl/fl mice. MED1ΔLiv mice also showed less weight gain on the high-fat diet compared with MED1fl/fl mice (Supporting Fig. 1D). These results suggest that MED1 deficiency increases glucose

tolerance and insulin sensitivity. PPARγ, when overexpressed in liver, induces adipogenic hepatic steatosis along with increased expression of adipocyte-specific as well as lipogenesis-related genes.6 To investigate the role of MED1 in PPARγ-stimulated HSP assay hepatic steatosis, we have used the conditional MED1 liver knockout mice.20 As expected, MED1fl/fl mice injected intravenously with 1 × 1011 adenovirus-PPARγ (Ad/PPARγ) particles revealed severe hepatic steatosis (Fig. 2A).6 In contrast, PPARγ overexpression failed to induce hepatic steatosis in MED1ΔLiv mouse (Fig. 2A). MED1ΔLiv mouse liver with PPARγ overexpression appeared essentially similar to the livers of uninjected

MED1ΔLiv mice or those injected with Ad/β-galactosidase (Ad/LacZ) (Fig. 2A,B). Hematoxylin and eosin www.selleck.co.jp/products/BafilomycinA1.html (H&E) and Oil Red O staining revealed no lipid accumulation in the MED1ΔLiv mouse liver except for a few large hepatocytes that escaped Cre-mediated gene deletion (Fig. 2C,D). In contrast, PPARγ overexpression in MED1fl/fl mouse liver resulted in a marked accumulation of lipid in hepatocytes (Fig. 2C,D). Immunohistochemical analysis confirmed MED1 nuclear staining in all hepatic parenchymal cells in MED1fl/fl mice, whereas only an occasional liver nucleus stained positive for MED1 in MED1ΔLiv mouse liver (Fig. 2C; MED1 IHC). In PPARγ overexpressing MED1fl/fl and MED1ΔLiv mouse livers nuclear localization of PPARγ was evident by immunohistochemistry (Supporting Fig. 2). In uninjected MED1fl/fl control livers, nuclear staining of PPARγ was not evident.