Molecular mechanism of inflammatory cytokine induction by hepatitis viruses
Molecular mechanism of inflammatory cytokine induction by hepatitis viruses
批准号:
12670462
负责人:
KATO Naoya
金额:
$2.5万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2001
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Hepatitis viruses cause persistent infection, chronic hepatitis, cirrhosis, and hepatocellular carcinoma. In this study, the influence of hepatitis B, C, and delta virus (HBV, HCV, and HDV, respectively) proteins on the function of hepatocyte, especially the induction of inflammatory cytokines, was investigated. Among 15 viral proteins, HCV core protein activated NF-_KB, AP-1, MAP kinase, and P53-associated signaling pathways. HCV core protein upregulated interleukin-16 and -8 promoters through NF-_KB activation, and increased p21 expression through p53 activation. The core protein activated NF-_KB pathway through IKKβand tumor necrosis factor receptor-associated factor (TRAF), and enhanced p53 function through augmentation of DNA-binding affinity and transcriptional ability. The core protein may directly promote cell proliferation and induce an inflammatory reaction by activating NF-_KB, AP-1, and MAP kinase-assosiated signaling pathways. On the other hand, the core protein could enha … More nce p53 function. These opposing functions may result in exquisitely balancing the proliferation of hepatocytes infected with HCV.Apoptosis is related to inflammation of the liver in chronic hepatitis. In HCV core protein-expressing cell, activation of caspase 3 was inhibited and Bcl-x_L expression was increased. The core protein enhances the Bcl-x_L expression through activating MAP kinase cascade, and thus inhibits apoptotic signal induced by Fas at the mitochondria level. Core protein-mediated Bcl-x_L induction may be one of the mechanisms underlying its inhibition of apoptosis, which might contribute to the pathogenesis of HCV.HCV NS4A and NS4B proteins generally suppressed cellular translation process (translational shutoff). This function may be involved in HCV infection and help its survival in host cells. In addition to HCV proteins, HDV large antigen activated SRF-associated pathway and synergistically activated SRE with HBx protein.In summary, hepatitis virus proteins may influence intracellular signaling pathways, induce inflammatory cytokines, and thus cause inflammation of the liver. Less
期刊论文(26)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
Kato N et al.: "Activation of intracelluar signaling by hepatity B & C viruses : C-viral core is the most potent signal inducer"Hepatology. 32. 405-412 (2000)
Kato N 等人:“乙型肝炎激活细胞内信号传导
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Kato J et al.: "Hepatitis C virus NS4A and NS4B protein suppress translation in vivo"J Med Viral. 66. 187-199 (2002)
Kato J 等人:“丙型肝炎病毒 NS4A 和 NS4B 蛋白抑制体内翻译”J Med Viral。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Kato J, Kato N, Yoshida H, Ono-Nita SK, Shiratori Y, Omata M: "Hepatitis C virus NS4A and NS4B proteins suppress translation in vivo"J Med Virol. 66. 187-199 (2002)
Kato J、Kato N、Yoshida H、Ono-Nita SK、Shiratori Y、Omata M:“丙型肝炎病毒 NS4A 和 NS4B 蛋白抑制体内翻译”J Med Virol。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Kato J, et al.: "hepatitis c-virus NS4A and NS4B proteins suppress trouslation in vivo"J Med Vivol. 66. 187-199 (2002)
Kato J 等人:“丙型肝炎病毒 NS4A 和 NS4B 蛋白抑制体内 trouslation”J Med Vivol。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Ono SK, Kato N, Shiratori Y, Kato J, Goto T, Scinazi RF, Carrilho FJ, Omata M: "The polymerase L528M mutation cooperates with nucleotide binding-site mutations, increasing hepatitis B virus replication and drug resistance"J Clin Invest. 107. 449-455 (2001
Ono SK、Kato N、Shiratori Y、Kato J、Goto T、Scinazi RF、Carrilho FJ、Omata M:“聚合酶 L528M 突变与核苷酸结合位点突变协同作用,增加乙型肝炎病毒复制和耐药性”J Clin Invest。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
共 25 条
Interferon stimulated genes and its polymorphisms determining Hepatitis C virus replication and pathogenesis of hepatitis C
-
批准号:20590760
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$3.0万
-
财政年份:2008
-
负责人:KATO Naoya
-
依托单位:
Comprehensive analysis of hepatitis Cvirus protein that disturb host interferon system
-
批准号:18590718
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.57万
-
财政年份:2006
-
负责人:KATO Naoya
-
依托单位:
Analyses of the individual risk for hepatocellular carcinoma by large scale search of single nucleotide polymorphisms of cytokine genes
-
批准号:16590578
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.24万
-
财政年份:2004
-
负责人:KATO Naoya
-
依托单位:
Viral mutations and host diversities that contribute to hepatocarcinogenesis
-
批准号:14570449
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.24万
-
财政年份:2002
-
负责人:KATO Naoya
-
依托单位:
海外基金