期刊文献+

脂滴代谢与丙型肝炎病毒生活周期关联的研究进展 被引量:1

Progress in the study of the association between the lipid droplets and hepatitis C virus life cycle
原文传递
导出
摘要 脂滴(lipid droplets, LDs)是广泛存在的动态细胞器,它们在所有真核细胞和部分原核细胞中储存和供应脂质,用于能量代谢与脂膜合成等。越来越多的证据表明,丙型肝炎病毒(hepatitis C virus, HCV)由于自身缺乏脂质生物合成途径而发生了进化,使其能够利用宿主脂质代谢途径,建立适宜自身增殖的环境而获得必要的成分,最终促进病毒组装和运输。本文主要对HCV生活周期与脂滴生物合成及代谢之间的关联做一综述,以期为HCV引起的相关疾病及其治疗的研究提供线索。 Lipid droplets(LDs) are ubiquitous dynamic organelles that store and supply lipids in all eukaryotic and some prokaryotic cells for energy metabolism, membrane synthesis and production of essential lipid-derived molecules. There is increasing evidence that hepatitis C virus(HCV) has co-evolved due to its lack of lipid biosyn‐thetic pathways to utilize host lipid metabolic pathways to establish a suitable environment for virus proliferation and obtain the necessary components, eventually promote the assembly and transportation of virus. In this review,we outline the relationship between HCV life cycle and lipid droplet biosynthesis and metabolism, with the aim to discover potential antiviral targets for development of new therapeutic interventions.
作者 安妮 衣岽戎 李晓宇 岑山 AN Ni;YI Dong-rong;LI Xiao-yu;CEN Shan(Institute of Medicinal Biotechnology,Chinese Academy of Medical Sciences and Peking Union Medical College,Beijing 100050,China)
出处 《药学学报》 CAS CSCD 北大核心 2019年第3期393-398,共6页 Acta Pharmaceutica Sinica
基金 国家自然科学基金委面上项目(81772205) 国家重点研发计划重点专项(2016YFD0500307)
关键词 脂滴 丙型肝炎病毒 脂代谢 黄病毒 脂滴相关蛋白 lipid droplet hepatitis C virus lipid metabolism flaviviridae lipid droplets-associated protein
  • 相关文献

参考文献2

二级参考文献103

  • 1PILERI P, UEMATSU Y, CAMPAGNOLI S, et al. Binding of hepatitis C virus to CDS1 [J]. Science, 1998,282 (5390) :938 - 941.
  • 2SCARSELLI E, ANSUINI H, CERINO R., et al. The human scavenger receptor class B type I is a novel candidate receptor for the hepatitis C virus[J]. EMBO J, 2002, 21 (19):5017 - 5025.
  • 3BENEDICTO I, MOLINA-JIMENEZ F, BARTOSCH B, et al. The tight junction-associated protein oceludin is required for a postbinding step in hepatitis C virus entry and infection [ J ]. J Virol, 2009,83 (16) :8012 - 8020.
  • 4EVANS MJ, VON HAHN T, TSCHERNE DM, et al. Claudin-I is a hepatitis C virus coreeeptor required for a late step in entry [J]. Nature,2007, 446(7137) :801 - 805.
  • 5SYDER A J, LEE H, ZEISEL MB, et al. Small molecule scaven- ger receptor BI antagonists are potent HCV entry inhibitors[ J]. J Hepatol, 2011,54 ( 1 ) :48 - 55.
  • 6ZHU HH, WONG-STAAL F, LEE H, et al. Evaluation of ITX5061, a scavenger receptor BI antagonists: resistance selec- tion and activity in combination with other hepatitis C virus antivi- rals [ J ]. J Infect Dis, 2012,205 (4) : 656 - 662.
  • 7LUBAN J. Absconding with the chaperone: essential cyclophilin- gag interaction in HIV-1 virions [ J ]. Cell, 1996, 87 ( 7 ) :1157 -1159.
  • 8HANDSCHUMACHER RE, HARDING MW, RICE J, et al. Cy- clophilin: a specific cytosolic binding protein for cyclosporin A [ J ]. Science, 1984,226 (4674) :544 - 547.
  • 9COELMONT L, KAPTEIN S, PAESHUYSE J, et al. Debio 025, a cyclophilin binding molecule, is highly efficient in clearing hepatitis C virus (HCV) replicon-containing ceils when used a- lone or in combination with specifically targeted antiviral therapy for HCV (STAT-C) inhibitors [ J]. Antlmicrob Agents Chemoth- er, 2009,53 ( 3 ) : 967 - 976.
  • 10BILLICH A, HAMMERSCHMID F, PEICHL P, et al. Mode of action of SDZ NIM 811, a nonimmunosuppressive cyclosporin A analog with activity against human immunodeficiency virus (HIV) type 1 interference with HIV protein-cyclophilin A inter- actions [ J ]. J Virol, 1995,69 (4) : 2451 - 2461.

共引文献3

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部