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JAK/STAT信号通路在刀豆蛋白A诱导的自身免疫性肝炎中的作用 被引量:6

Role of JAK/STAT Signal Pathway in Con A-induced Autoimmune Hepatitis
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摘要 自身免疫性肝炎(autoimmune hepatitis,AIH)是一种由肝脏组织耐受性缺失导致的慢性炎症性疾病.刀豆蛋白A(concanavalin A,Con A)是一种提取自刀豆的植物凝集素.由Con A诱导的肝炎模型常用于研究AIH的动物模型.JAK激酶(janus-activated kinases,JAK)/信号传导与转录激活子(signal transducer and activator of transcription,STAT)信号通路是在该模型中研究比较多的细胞内信号转导通路.该模型中的关键细胞因子IFN-γ、IL-4、IL-12、IL-6及IL-22均可以通过JAK/STAT信号通路发挥作用.本文综述了IFN-γ/STAT1信号通路、IL-4/STAT6信号通路、IL-12/STAT4信号通路参与Con A诱导肝损伤产生的机制,同时综述了IL-6/STAT3信号通路、IL-22/STAT3信号通路对肝损伤的保护作用及可能的机制. Autoimmune hepatitis(AIH) is a chronic inflammatory disease in which a loss of tolerance of hepatic tissue is presumed. The concanavalin A(Con A)-induced autoimmune hepatitis model in mice is a well established and widely used model for investigating the pathogenesis mechanisms and pathological changes of T-cell dependent liver injury. Janus-activated kinases/signal transducer and activator of transcription(JAK/STAT)signal pathway paly a critical role for intracellular signal transduction in this model. The relevant literatures concerning the mechanism of the IFN-γ/STAT1 signal pathway, IL-4/STAT6 signal pathway and IL-12/STAT4 signal pathway which involved in Con A-induced hepatitis and the role of the IL-6/STAT3 signal pathway and IL-22/STAT3 signal pathway in protecting against Con A-induced hepatitis were reviewed in this article.
作者 李莎 马丽杰 LI Sha MA Li-Jie(Deparmen,t of Pharmacology, The Inner Mongolia Medical University, Hohhot 010059, China)
出处 《生物化学与生物物理进展》 SCIE CAS CSCD 北大核心 2016年第12期1139-1145,共7页 Progress In Biochemistry and Biophysics
基金 国家自然科学基金资助项目(81360676)~~
关键词 JAK/STAT信号通路 刀豆蛋白A 自身免疫性肝炎 JAK/STAT signal pathway, concanavalin A, autoimmune hepatitis
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  • 1Lei Yang Yong-feng Liu Shu-rong Liu Gang Wu Jia-lin Zhang Yi-man Meng Shao-wei Shong Gui-chen Li.PREVENTION AND TREATMENT OF REJECTION AFTER SIMULTANEOUS PANCREAS-KIDNEY TRANSPLANTATION[J].Chinese Medical Sciences Journal,2005,20(3):210-213. 被引量:3
  • 2Dumoutier L, Louahed J, Renauld JC. Cloning and characterizationof IL-10-related T cell-derived inducible factor (IL-TIF),a novel cytokine structurally related to IL-10 and inducible byIL-9. J Immunol 2000; 164: 1814-1819 [PMID: 10657629 DOI:10.4049/jimmunol.164.4.1814].
  • 3Ki SH, Park O, Zheng M, Morales-Ibanez O, Kolls JK, Bataller R,Gao B. Interleukin-22 treatment ameliorates alcoholic liver injuryin a murine model of chronic-binge ethanol feeding: role of signaltransducer and activator of transcription 3. Hepatology 2010; 52:1291-1300 [PMID: 20842630 DOI: 10.1002/hep.23837].
  • 4Yang L, Zhang Y, Wang L, Fan F, Zhu L, Li Z, Ruan X, HuangH, Wang Z, Huang Z, Huang Y, Yan X, Chen Y. Amelioration ofhigh fat diet induced liver lipogenesis and hepatic steatosis byinterleukin-22. J Hepatol 2010; 53: 339-347 [PMID: 20452699DOI: 10.1016/j.jhep.2010.03.004].
  • 5Zenewicz LA, Yancopoulos GD, Valenzuela DM, Murphy AJ,Karow M, Flavell RA. Interleukin-22 but not interleukin-17provides protection to hepatocytes during acute liver inflammation.Immunity 2007; 27: 647-659 [PMID: 17919941 DOI: 10.1016/j.immuni.2007.07.023].
  • 6Radaeva S, Sun R, Pan HN, Hong F, Gao B. Interleukin 22 (IL-22)plays a protective role in T cell-mediated murine hepatitis: IL-22 isa survival factor for hepatocytes via STAT3 activation. Hepatology2004; 39: 1332-1342 [PMID: 15122762 DOI: 10.1002/hep.20184].
  • 7Ren X, Hu B, Colletti LM. IL-22 is involved in liver regenerationafter hepatectomy. Am J Physiol Gastrointest Liver Physiol 2010;298: G74-G80 [PMID: 19875704 DOI: 10.1152/ajpgi.00075.2009].
  • 8Boniface K, Bernard FX, Garcia M, Gurney AL, Lecron JC,Morel F. IL-22 inhibits epidermal differentiation and inducesproinflammatory gene expression and migration of humankeratinocytes. J Immunol 2005; 174: 3695-3702 [PMID: 15749908DOI: 10.4049/jimmuol.174.6.3695].
  • 9Brand S, Beigel F, Olszak T, Zitzmann K, Eichhorst ST, OtteJM, Diepolder H, Marquardt A, Jagla W, Popp A, Leclair S,Herrmann K, Seiderer J, Ochsenkühn T, G-ke B, AuernhammerCJ, Dambacher J. IL-22 is increased in active Crohn's disease andpromotes proinflammatory gene expression and intestinal epithelialcell migration. Am J Physiol Gastrointest Liver Physiol 2006; 290:G827-G838 [PMID: 16537974 DOI: 10.1152/ajpgi.00513.2005].
  • 10Chung Y, Yang X, Chang SH, Ma L, Tian Q, Dong C. Expressionand regulation of IL-22 in the IL-17-producing CD4+ Tlymphocytes. Cell Res 2006; 16: 902-907 [PMID: 17088898 DOI:10.1038/sj.cr.7310106].

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