The suppressed translocation of Parkin to the mitochondria inhibited mitochondrial ubiquitination’decreased the number of mitochondria sequestered in isolation

membranes (mitophagosomes), and reduced autophagic degradation activity, which clearly indicated the suppression of mitophagy. However, OR6 cells promoted autophagy under non-selective autophagyinducible conditions (amino acid starvation), as indicated by the increased expression Dorsomorphin in vivo of the microtubule-associated protein light chain 3 (LC3)-II. CONCLUSIONS: Through a direct interaction with Parkin, the HCV core protein suppressed mitophagy by inhibiting the translocation of Parkin to the mitochondria. These results have implications for the amplification and sustainability of mitochondria-induced oxidative stress observed in patients with HCV-related chronic liver disease and an increased risk of hepatocarcinogenesis. Disclosures: Kazuaki Chayama – Consulting:

Abbvie; Grant/Research Support: Dainippon Sumitomo, Chugai, Mitsubishi Tanabe, DAIICHI SANKYO, Toray, BMS, MSD; Speaking and Teaching: Chugai, Mitsubishi Tanabe, Histone Methyltransferase inhibitor DAIICHI SANKYO, KYORIN, Nihon Medi-Physics, BMS, Dainippon Sumitomo, MSD, ASKA, Astellas, AstraZeneca, Eisai, Olympus, GlaxoSmithKline, ZERIA, Bayer, Minophagen, JANSSEN, JIMTO, TSUMUTA, Otsuka, Taiho, Nippon Kayaku, Nippon Shinyaku, Takeda, AJINOMOTO, Meiji Seika, Toray The following people have nothing to disclose: Yuichi Hara, Sohji Nishina, Izumi Yanatori, Masanori Ikeda, Emi Kiyokage, Yasuyuki Tomiyama, Kazunori Toida, Fumio Kishi, Nobuyuki Kato, Michio Imamura, Keisuke Hino Aims: To investigate the role of the flavonoid quercetin (Q) on modulation of lipid droplets (LDs) size and morphology

and HCV core protein localization and (3) HCV life cycle focusing on Fossariinae entry and replication. Methods: The morphology of LDs and core localisation were studied by immunofluorescence using confocal microscopy on Huh-7 cells transduced with lentivectors encoding the core protein of HCV genotype3a and treated with quercetin for 48h at different concentrations (50μM-100μM). LDs analysis was done using MetaMorph Microscopy-Software. To study the effects of quercetin on viral replication (iRNA), Huh7 cells were infected with Jc1 ccHCV particles (1Moi) and subsequently treated with quercetin for 48 and 72h. NS3 and core protein levels were evaluated by immunoblot. HCV entry was assessed using HCV pseudoparticies(HCVpp), which are lentivectors harboring HCV entry proteins and containing luciferase as reporter gene. Results: LDs morphology(area, radium, and volume) and distribution were modified by quercetin in Huh7. Quercetin treatment could impede the core 3a- induced increase of LD size in cells transduced with lentivirus expressing the Core genotype 3a protein [LD area (μm2): 3a:109.8±33.72; 3aQ50μM: 79.90±36(p<0.001); 3aQ100μM: 72, 6±35.4(p<0, 0003); radium(μm): 3a: 5.85±0.88; 3aQ50μM: 4.91 ±1.15(p<0.001) 3aQ100μM: 4.65±1.22 (p<0.0002), voiumen (μm3) 3a: 894.7±418.5; 3aQ50μM: 577.03±379.