期刊文献+

新基因丙型肝炎病毒核心蛋白结合蛋白6的发现和研究——献礼非酒精性脂肪性肝病 被引量:3

Discovery and study of hepatitis C virus core protein binding protein 6——contribution to non-alcoholic fatty liver diseases
暂未订购
导出
摘要 丙型肝炎病毒核心蛋白结合蛋白6(hepatitis C virus core protein binding protein 6,HCBP6)是成军教授课题组利用酵母双杂交技术首先发现的与丙型肝炎病毒核心蛋白结合的蛋白。课题组进一步发现HCBP6可以感受肝细胞内总胆固醇与甘油三酯水平变化并调节总胆固醇与甘油三酯水平。动物模型发现,HCBP6基因敲除小鼠在高脂饮食喂养下会出现糖脂代谢紊乱。课题组进而发现韩国红参组分可通过调节HCBP6改善糖脂代谢,推动了含有该组分PTIB001的治疗非酒精性脂肪性肝病(nonalcholic fatty liver disease,NAFLD)的功能食品的问世。这些工作为基于PTIB001的治疗NAFLD药物研发提供了理论依据。 Hepatitis C virus(HCV) core protein binding protein 6(HCBP6) is first identified by Professor Cheng Jun’s team as a protein binding to HCV core protein with the yeast two hybrid system. Professor Cheng’s team further found that HCBP6 can sensor the fluctuation of total cholesterol and triglyceride and help to maintain the homeostasis of lipid metabolism and glycometabolism. Homozygous HCBP6 knock-out mouse showed abnormal lipid metabolism and glycometabolism on high fat diet feeding. Professor Cheng’s team found that PTIB001 from Korean red ginseng might help to maintain homeostasis of lipid metabolism and glycometabolism through HCBP6 pathway. Professor Cheng’s team enhanced the development of functional food which contain PTIB001 for non-alcoholic fatty liver disease(NAFLD). These work provide theoretical evidence for the development of PTIB001 related agents for NAFLD.
作者 成军 CHENG Jun(Center of Liver Diseases,Beijing Ditan Hospital,Capital Medical University,Beijing 100015,China)
出处 《中国肝脏病杂志(电子版)》 CAS 2019年第4期1-4,共4页 Chinese Journal of Liver Diseases:Electronic Version
基金 北京市自然科学基金重点项目(7161006) 北京市医院管理局“登峰”计划专项经费资助(DFL20151701) 国家自然科学基金青年科学基金项目(81700508)
关键词 丙型肝炎病毒核心蛋白结合蛋白6 非酒精性脂肪性肝病 脂代谢 人参 HCV core protein binding protein 6 Fatty liver disease,non-alcoholic Lipid metabolism Ginseng
  • 相关文献

参考文献3

二级参考文献68

  • 1成军.HCV RNA定量PCR检测研究进展[J].国外医学(流行病学.传染病学分册),1994,21(1):20-23. 被引量:8
  • 2成军.丙型肝炎病毒基因组的翻译及其产物的加工[J].国外医学(微生物学分册),1995,18(4):14-16. 被引量:21
  • 3Michael C, Stephen TS. Transcriptional regulation in eukaryotes.New York: Cold Spring Harbor. 1999. 5-12.
  • 4Maniatis T, Whittemore LM, Keller AD, et al. Transctiptional regulation. New York: Cold Spring Harbor. 1992. 953-962.
  • 5Bach N, Thung SN, Schaffner F. The histological featuresof chronic hepatitis C and autoimmune chronic hepatitis: acomparative analysis. Hepatology 1992; 15: 572-577 [PMID:1551632 DOI: 10.1002/hep.1840150403].
  • 6Westin J, Nordlinder H, Lagging M, Norkrans G, Wejst R.Steatosis accelerates fibrosis development over time in hepatitis Cvirus genotype 3 infected patients. J Hepatol 2002; 37: 837-842[PMID: 12445426 DOI: 10.1016/S0168-8278(02)00299-4].
  • 7Khan M, Jahan S, Khaliq S, Ijaz B, Ahmad W, Samreen B,Hassan S. Interaction of the hepatitis C virus (HCV) core withcellular genes in the development of HCV-induced steatosis. ArchVirol 2010; 155: 1735-1753 [PMID: 20842391 DOI: 10.1007/s00705-010-0797-7].
  • 8Reed KE, Rice CM. Overview of hepatitis C virus genomestructure, polyprotein processing, and protein properties. Curr TopMicrobiol Immunol 2000; 242: 55-84 [PMID: 10592656 DOI:10.1007/978-3-642-59605-6_4].
  • 9Moriya K, Nakagawa K, Santa T, Shintani Y, Fujie H, MiyoshiH, Tsutsumi T, Miyazawa T, Ishibashi K, Horie T, Imai K,Todoroki T, Kimura S, Koike K. Oxidative stress in the absenceof inflammation in a mouse model for hepatitis C virus-associatedhepatocarcinogenesis. Cancer Res 2001; 61: 4365-4370 [PMID:11389061].
  • 10Moriya K, Yotsuyanagi H, Shintani Y, Fujie H, Ishibashi K,Matsuura Y, Miyamura T, Koike K. Hepatitis C virus core proteininduces hepatic steatosis in transgenic mice. J Gen Virol 1997; 78 (Pt 7): 1527-1531 [PMID: 9225025].

共引文献45

同被引文献22

引证文献3

二级引证文献68

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