Role of seipin in lipid droplet morphology and hepatitis C virus life cycle

被引:10
作者
Clement, Sophie [1 ]
Fauvelle, Catherine [3 ]
Branche, Emilie [3 ]
Kaddai, Vincent [3 ]
Conzelmann, Stephanie [3 ]
Boldanova, Tujana [4 ]
Bartosch, Birke [5 ]
Minehira, Kaori [6 ]
Negro, Francesco [1 ,2 ]
机构
[1] Univ Geneva, Sch Med, Univ Hosp, Div Clin Pathol, CH-1211 Geneva, Switzerland
[2] Univ Geneva, Sch Med, Univ Hosp, CH-1211 Geneva, Switzerland
[3] Univ Geneva, Fac Med, Dept Pathol & Immunol, Geneva, Switzerland
[4] Univ Basel Hosp, Dept Biomed, Basel, Switzerland
[5] Univ Lyon, CNRS 5286, INSERM U1052, CRCL, Lyon, France
[6] Univ Lausanne, Dept Physiol, Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
FATTY-ACID SYNTHASE; DIACYLGLYCEROL ACYLTRANSFERASE-1; CONGENITAL LIPODYSTROPHY; CORE PROTEIN; YEAST; DIFFERENTIATION; PATHOGENESIS; ACTIVATION; EXPRESSION; STEATOSIS;
D O I
10.1099/vir.0.054593-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Infectious hepatitis C virus (HCV) particle assembly starts at the surface of lipid droplets, cytoplasmic organelles responsible for neutral fat storage. We analysed the relationship between HCV and seipin, a protein involved in lipid droplet maturation. Although seipin overexpression did not affect the total mean volume occupied by lipid droplets nor the total triglyceride and cholesterol ester levels per cell, it caused an increase in the mean diameter of lipid droplets by 60%, while decreasing their total number per cell. The latter two effects combined resulted in a 34% reduction of the total outer surface area of lipid droplets per cell, with a proportional decrease in infectious viral particle production, probably due to a defect in particle assembly. These results suggest that the available outer surface of lipid droplets is a critical factor for HCV release, independent of the neutral lipid content of the cell.
引用
收藏
页码:2208 / 2214
页数:7
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