UBXD8 KO mice showed a significant decrease in the VLDL-TG secretion in comparison to WT mice (553 mg/dl/h vs. 739 mg/dl/h, P=0.006). (5) The

Apo B secretion was directly measured by using primary hepatocytes from WT and KO mice. Hepatocytes of KO mice secreted a significantly less amount of ApoB than hepatocytes of WT mice. The decrease of ApoB secretion in hepatocytes of KO mice was more evident when 0.4 mM oleic acid was added to the culture medium. [Conclusion] The VLDL secretion in hepatocytes is known to be regulated mainly by posttrans-lational selleck inhibitor degradation of ApoB. The present study showed that UBXD8 plays a critical role in the regulation of VLDL secretion in mouse liver in vivo and that depletion of UBXD8 causes a decrease of VLDL secretion and steatosis. buy 3-deazaneplanocin A Interestingly, UBXD8-KO mice on the high-fat diet showed

macrovesicular steatosis mainly in zone 1. This is in contrast with non-alcoholic fatty liver disease, which primarily presents steatosis in zone 3. The unique phenotype of UBXD8-KO mice warrants further studies to elucidate the mechanism behind steatosis. Disclosures: Hidemi Goto – Grant/Research Support: MSD, Roche, Bayer, Bristol-Myers, Eisai, Ajinomoto, Otsuka, Astra, Tanabe The following people have nothing to disclose: Norihiro Imai, Michitaka Suzuki, Yoji Ishizu, Teiji Kuzuya, Takashi Honda, Kazuhiko Hayashi, Masatoshi Ishi-gami, Toyoshi Fujimoto Background: this website Fatty liver is associated with ER stress and activation of the hepatic Unfolded Protein Response (UPR), including increased expression of the UPR regulator Xbp1s. Reduced hepatic expression of human XBP1s is associated with NASH compared to bland NAFLD (Gastro 2008) and feeding a high fat diet with high fructose (corn syrup equivalent) to mice has been shown to cause progressive steatohepatitis (AJP, 2011; AJP 2008). The aims of this study are to examine the role of Xbp1 in non-alcoholic fatty liver injury and fatty acid-induced cell injury. Methods: We have developed hepatocyte-specific Xbp1-deficient (Xbp1−/−) mice. A high fat western diet (AIN-76, TestDiet) and drinking

water with 55% fructose and 45% glucose (HFD/HF) (high fructose corn syrup equivalent) were fed to Xbp1−/− and Xbp1f/f control mice for 4 weeks. We performed RNA-Seq and real-time PCR on liver mRNA. We also assayed serum ALT, glucose, hepatic TG and histology. For in vitro study, we generated stable XBP1-knockdown Huh7 cells (Huh7/KD) and scramble Huh7 control cells (Huh7/SCR) and treated them with 400 palmitic acid (PA) for 24 hrs. Cell injury was measured by LDH and caspase 3/7 activity assays. Gene and protein expression was examined by real-time PCR and western blotting. Results: Xbp1−/− mice exhibited higher serum ALT levels 4 weeks after HFD/HF feeding compared to Xbp1f/f controls (70 ± 10 vs 23 ± 2 U/L, p<0.002).