• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Interferon signal transduction.

作者信息

Larner A, Reich N C

机构信息

Division of Cytokine Biology, Center for Biologics Evaluation and Research, Bethesda, MD 20892, USA.

出版信息

Biotherapy. 1996;8(3-4):175-81. doi: 10.1007/BF01877202.

DOI:10.1007/BF01877202
PMID:8813329
Abstract

The interferon signal transduction pathway initiates at a cell surface receptor and mediates the activation of target genes in the nucleus. The binding of interferon to a transmembrane receptor stimulates the activation of associated tyrosine kinases of the Janus kinase (JAK) family. Subsequently, latent cytoplasmic transcription factors are activated by tyrosine phosphorylation and function as signal transducers and activators of transcription (STATs). Advances in the field of interferon research have contributed to our understanding of signal transduction induced by many cytokines that also use JAK/STAT signaling pathways to activate early response genes. The specificity of signal activation by distinct cytokines that share these signaling components, and the molecular interaction of the signaling components with each other and their respective cytokine receptors represent major areas of research that are beginning to be elucidated. Signaling molecules other than the JAKs and STATs have also been found to be activated following interferon binding. In addition, the induction of type I interferon stimulated genes by double-stranded RNA in the absence of interferon provides another pathway of specific gene activation.

摘要

相似文献

1
Interferon signal transduction.
Biotherapy. 1996;8(3-4):175-81. doi: 10.1007/BF01877202.
2
Signal transduction and activation of gene transcription by interferons.干扰素介导的信号转导与基因转录激活
Gene Expr. 1995;5(1):1-18.
3
Signal transduction in the interferon system.
Semin Oncol. 1998 Feb;25(1 Suppl 1):14-22.
4
The Jak-STAT pathway: cytokine signalling from the receptor to the nucleus.Jak-STAT信号通路:从受体到细胞核的细胞因子信号传导
J Recept Signal Transduct Res. 1999 Jan-Jul;19(1-4):75-120. doi: 10.3109/10799899909036638.
5
[Interferon signaling pathways].[干扰素信号通路]
Bull Cancer. 1999 Nov;86(11):911-9.
6
JAKs, STATs and signal transduction in response to the interferons and other cytokines.JAKs、STATs与干扰素及其他细胞因子应答中的信号转导
Philos Trans R Soc Lond B Biol Sci. 1996 Feb 29;351(1336):167-71. doi: 10.1098/rstb.1996.0013.
7
The structure, regulation and function of the Janus kinases (JAKs) and the signal transducers and activators of transcription (STATs).Janus激酶(JAKs)以及信号转导子和转录激活子(STATs)的结构、调控与功能。
Eur J Biochem. 1997 Sep 15;248(3):615-33. doi: 10.1111/j.1432-1033.1997.00615.x.
8
PDGF stimulates tyrosine phosphorylation of JAK 1 protein tyrosine kinase in human mesangial cells.血小板衍生生长因子刺激人系膜细胞中JAK 1蛋白酪氨酸激酶的酪氨酸磷酸化。
Kidney Int. 1996 Jan;49(1):19-25. doi: 10.1038/ki.1996.3.
9
The immunohistochemical localization of stat-2, -3, -4 and -5 during early enamel and dentine formation in rat molars.
Arch Oral Biol. 1996 Dec;41(12):1149-60. doi: 10.1016/s0003-9969(96)00084-2.
10
IL-3 signaling and the role of Src kinases, JAKs and STATs: a covert liaison unveiled.白细胞介素-3信号传导以及Src激酶、JAK激酶和信号转导及转录激活因子的作用:揭示一种隐秘联系
Oncogene. 2000 May 15;19(21):2532-47. doi: 10.1038/sj.onc.1203594.

引用本文的文献

1
Molecular mechanisms of viral hepatitis induced hepatocellular carcinoma.病毒性肝炎诱导肝细胞癌的分子机制。
World J Gastroenterol. 2020 Oct 14;26(38):5759-5783. doi: 10.3748/wjg.v26.i38.5759.
2
Life cycle and pathogenesis of hepatitis D virus: A review.丁型肝炎病毒的生命周期与发病机制:综述
World J Hepatol. 2013 Dec 27;5(12):666-75. doi: 10.4254/wjh.v5.i12.666.
3
Ligand-stimulated downregulation of the alpha interferon receptor: role of protein kinase D2.配体刺激的α干扰素受体下调:蛋白激酶 D2 的作用。
Mol Cell Biol. 2011 Feb;31(4):710-20. doi: 10.1128/MCB.01154-10. Epub 2010 Dec 20.
4
UBP43 is a novel regulator of interferon signaling independent of its ISG15 isopeptidase activity.UBP43是一种新型的干扰素信号调节因子,与其ISG15异肽酶活性无关。
EMBO J. 2006 Jun 7;25(11):2358-67. doi: 10.1038/sj.emboj.7601149. Epub 2006 May 18.
5
Novel type I interferon IL-28A suppresses hepatitis C viral RNA replication.新型I型干扰素IL-28A可抑制丙型肝炎病毒RNA复制。
Virol J. 2005 Sep 7;2:80. doi: 10.1186/1743-422X-2-80.