期刊文献+

β-arrestin 2在免疫调节中的作用 被引量:3

The role of β-arrestin 2 in immune regulation PENG Ai'ni1, YAN Fuling2,
下载PDF
导出
摘要 β-arrestin2是一类arrestin家族成员,它不仅参与调节G蛋白偶联受体(G protein-coupled receptors,GPCRs)的脱敏和内化,还可以作为支架蛋白转导信号通路。目前研究证实,β-arrestin 2可以通过多种途径调节免疫反应,如抑制NF-κB活化、调节趋化因子受体介导的免疫细胞趋化等,同时还参与了多种免疫相关疾病、肿瘤以及炎症的发生和发展。本文就β-arrestin 2在免疫调节中的作用进行综述。 β-arrestin 2 is one member of arrestin family, which not only causes desensitization and internalization of G protein-coupled receptors (GPCRs), but also serves as a scaffold protein in signal transduction. Now it has been demonstrated that β-arrestin 2 can regulate immune responses through multiple mechanisms, such as inhibiting NF-KB activation and regulating chemokine receptor-mediated cbemotaxis of immune cells. And β- arrestin 2 also participates in the occurrence and development of various immune-related diseases, cancers and inflammation. This paper will elaborate the functions of β-arrestin 2 in regulating immune responses.
出处 《免疫学杂志》 CAS CSCD 北大核心 2014年第2期170-174,共5页 Immunological Journal
基金 国家自然科学基金(81271336) 南京市科技局国际合作项目(201201105)
关键词 Β-ARRESTIN 2 免疫相关疾病 肿瘤 炎症 β-arrestin 2 Immune-related diseases Cancer Inflammation
  • 相关文献

参考文献2

二级参考文献41

  • 1Heng Fan,Ming-Yi Qiu,Jia-Jun Mei,Guan-Xin Shen,Song-Lin Liu,Rui Chen.Effects of four regulating-intestine prescriptions on pathology and ultrastructure of colon tissue in rats with ulcerative colitis[J].World Journal of Gastroenterology,2005,11(31):4800-4806. 被引量:19
  • 2Ping Zheng,Feng-Li Niu,Wen-Zhong Liu,Yao Shi,Lun-Gen Lu.Anti-inflammatory mechanism of oxymatrine in dextran sulfate sodium-induced colitis of rats[J].World Journal of Gastroenterology,2005,11(31):4912-4915. 被引量:38
  • 3[1]Yoshie O, Imai T, Nomiyama H. Chemokines in immunity[J]. Adv Immunol, 2001,78:57-110.
  • 4[2]Cascieri MA, Springer MS. The chemokine/chemokine-receptor family: potential and progress for therapeutic interven-tion[J]. Curr Opin Chem Bio,2000,4(4):420-427.
  • 5[3]Christopherson K 2nd, Hromas R. Chemokine regulation of normal and pathologic immune responses[J]. Stem Cells,2001,19(5):388-396.
  • 6[4]Murphy PM, Baggiolini M, Charo IF. International union of pharmacology. XXII. Nomenclature for chemokine receptors[J]. Pharmacol Rev,2000,52(1): 145-176.
  • 7[5]Fernandez EJ, Lolis E. Structure, function, and inhibition of chemokines[J]. Annu Rev Pharmacol Toxicol,2002,42:469-499.
  • 8[6]Luo J, Luo Z, Zhou N, et al. Attachment of C-terminus of SDF-1 enhances the biological activity of its N-terminal peptide[J]. Bioch Biophy Res Communicat,1999,264(1):42-47.
  • 9[7]Amara A, Lorthioir O, Valenzuela A, et al. SDF-1( associates with heparin sulfates through the first β-strand of the chemokine[J]. J Bio Chem,1999,274(34):23 916-23 925.
  • 10[8]Campbell JJ,Butcher EC. Chemokines in tissue-specific and microenvironment-specific lymphocyte homing[J]. Cur Opin Immunol,2000,12(3):336-341.

共引文献63

同被引文献55

引证文献3

二级引证文献4

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