期刊文献+

集聚蛋白在免疫细胞中的表达及其意义 被引量:3

The expression and implication of agrin in immunocytes
暂未订购
导出
摘要 为研究在神经突触中发挥重要作用的突触调节蛋白集聚蛋白是否在免疫细胞中表达并影响淋巴细胞的活化。首先通过RT-PCR、荧光免疫组织化学和FACS分别从mRNA水平和蛋白水平观察集聚蛋白在各种免疫器官、细胞中的表达;通过实时定量PCR检测分析集聚蛋白的表达与淋巴细胞活化的关系;并构建针对集聚蛋白的反义质粒,从而进一步研究下调集聚蛋白的表达对淋巴细胞活化的影响。结果发现集聚蛋白广泛表达于脾脏、胸腺、淋巴结等多种免疫器官中并在T细胞、B细胞、imDC、mDC及巨噬细胞中均有表达,其表达含量与淋巴细胞的活化状态密切相关,且其表达被下调后淋巴细胞的活化显著被抑制。因而组成性表达于各种免疫细胞中的集聚蛋白可被诱导性上调,并参与了淋巴细胞的活化。 To study whether agrin, a synaptic regulated protein in neurological synapse, is expressed in immuno-cytes and affects the proliferation of lymphocyte. RT-PCR, immunofluorescence histochemistry and FACS were used to analyze the expression of agrin in some immune organs and primary immunocytes. Then real time RT-PCR and 3H-TdR incorporation assay were performed to evaluate the relationship between the expression of agrin and statue of lymphocyte activation. Constructed antisense plasmids were used to explore function of agrin in the proliferation of lymphocyte activation. Our experimental results demonstrated that agrin were constitutively expressed in various immune organs such as spleen, thymus and lymphonode, immunocytes including CD4+, CD8+ T cells, B220+ B cells, imDC, mDC, and MΦ. There was significant relationship between the expression of agrin and activation of lymphocytes. The proliferation of lymphocytes can be inhibited after the agrin expression being down regulated. These results suggest that constitutively expressed agrin in immunocytes participates in the proliferation of lymphocytes.
出处 《现代免疫学》 CAS CSCD 北大核心 2005年第2期102-107,共6页 Current Immunology
基金 上海市科委优秀学科带头人计划资助项目(04XD14003)国家杰出青年基金资助项目(39925031)国家"863"计划资助项目(2004AA215242)
关键词 集聚蛋白 反义CDNA 淋巴细胞的活化 agrin antisense cDNA lymphocytes activation
  • 相关文献

参考文献11

  • 1Grakoui A, Bromley SK, Sumen C, et al. The immunological synapse: a molecular machine controlling T cell activation[J]. Science, 1999, 285(5425):221-227.
  • 2Monks CR, Freiberg BA, Kupfer H, et al. Three-dimensional segregation of supramolecular activation clusters in T cells [J]. Nature, 1998, 395(6697):82-86.
  • 3Wulfing C, Sjaastad MD, Davis MM. Visualizing the dynamics of T cell activation: intracellular adhesion molecule 1 migrates rapidly to the T cell-B cell interface and acts to sustain calcium levels[J]. Proc Natl Acad Sci USA, 1998, 95(11):6302-6307.
  • 4Paul WE, Seder RA. Lymphocyte responses and cytokines[J]. Cell,1994, 76(2):241-251.
  • 5Dustin ML, Colman DR. Neural and inmunological synaptic relations[J]. Sicence, 2002, 298(5594):785-789.
  • 6Bezakova G, Ruegg MA. New insights into the roles of agrin[J].Nat Rev Mol Cell Biol, 2003, 4(4):295-308.
  • 7Inaba K, Inaba M, Romani N, et al. Generation of large numbers of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony-stimulating factor [J]. J Exp Med, 1992,176(6):1693-1702.
  • 8Godfey EW, Nitkin RM, Wallace BG, et al. Components of Torpedo electric organ and muscle that cause aggregation of acetycholine receptors on cultured muscle cells[J]. J Cell Biol, 1984,99(2):615-627.
  • 9Nitkin RM, Smith MA, Magill C, et al. Identification of agrin. a synaptic organizing protein, from Torpedo electric organ[J]. J Cell Biol, 1987,105(6):2471-2478.
  • 10Tordjman R, Lepelletire Y, Lemarchande V, et al. A neuronal receptor, neuropilin-1 is essential for the initiation of the primary immune response[J]. Nat Immunol, 2002, 3(5):477-482.

同被引文献53

  • 1王海燕.肾脏病学[M].北京:人民卫生出版社,2008:1948-1949.
  • 2Russo RN, Shaper NL, Shaper JH, et al. Bovine β-1 4- galaetosyltransferase: two sets of mRNA transcripts encode two forms of the protein with different amino-terminal domains: in vitro translation experiments demonstrate that both the short and the long forms of the enzyme are type Ⅱ membrane-bound glycoproteins[J]. J Biol Chem, 1990,265 : 3324- 3331.
  • 3Joziasse DH. Mammalian glycosyltransferases: genomic organization and protein structure[J]. Glycobiology, 1992,2: 271-277.
  • 4Nilsson T, Lucocq JM, Mackay D, et al. The membrane spanning domain of beta-l, 4-galactosyltransferase specifies trans-Golgi localization[J]. J EMBO, 1991,10 : 3567-3575.
  • 5Furukawa K, Sato T. Beta-1,4-Galactosylation of N-glycans is a complex process[J]. J Biochim Biophys Acta, 1999, 1473 : 54-66.
  • 6Trayer IP, Hill RL. The purification and properties of the A protein of lactose synthetase[J]. J Biol Cbem, 1971,246: 6666-6675.
  • 7Qian J, Cheng C, Liu H, et a l. Expression of beta-l,4- galactosyltrans-ferase I in rat during inflammation [J].Inflamma tion, 2007,30 : 59-68.
  • 8Shen A, Qian J, Liu L, et al. The role of beta 1,4 galacto syltransferase-I in the skin wound healing process[J]. Am J Dermatopathol, 2008,30 : 10-15.
  • 9Shen A, Chen J, Cheng C, et al. Elevated beta1,4-galacto- syltransferase-I induced by the intraspinal injection of lipopolysaccharide[J]. Glycocon J, 2009,26 : 19-31.
  • 10Rodeheffer C, Shur BD. Targeted mutations in 13-1,4-galactosyltransferase I reveal its multiple cellular functionsEJ]. Bioehim giophys Acta, 2002, 1573 : 258-270.

引证文献3

二级引证文献5

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