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小鼠CD4^+T细胞活化后IL-10受体Ⅰ表达的研究 被引量:2

The study of the IL-10 receptor Ⅰ expression level on the mouse CD4^+ T cell after stimulation
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摘要 目的:检测抗小鼠CD4+T淋巴细胞活化后表面白细胞介素10受体I(IL-10R1)表达变化,为进一步研究白细胞介素10(IL-10)相关免疫疾病的发病机制及进展提供有力支持。方法:取C57BL/6小鼠脾细胞,溶血后采用尼龙毛去除B淋巴细胞后,流式细胞仪无菌分选CD4+T淋巴细胞,利用anti-CD3和anti-CD28多克隆抗体刺激分选后细胞,分别在第0、12、24、48和72小时流式细胞术检测IL-10R1表达情况。结果:0小时时小鼠CD4+T淋巴细胞不表达IL-10R1,随着刺激时间的延长IL-10R1表达增加,24小时时达到最高,随后表达水平开始下降,72小时时表达情况与0小时基本相同。结论:CD4+T淋巴细胞活化后IL-10R1表达短暂,以24小时时表达最高。 Objective:To study the IL-10 receptor I(IL-10R1) expression level on the activated mouse CD4+ T cell and provide strong supply for studying the pathogenesis and progress of IL-10 related autoimmune diseases.Methods:The spleen cells of C57BL/6 mouse were isolated and B cells was got rid of by nylon filter after hemolysis.CD4+T cells were isolated sterilely by flow cytometry.The IL-10R1 level was detected on the CD4+T cell at the 0th,12th,24th,48th and 72th hour by flow cytometry after stimulation by anti-CD3 and anti-CD28 polyclonal antibody.Results:At the 0th hour CD4+T cell did not express IL-10R1.With the extension of time the level of IL-10R1 were increased and at the 24th hour reached the peak.Then the level of IL-10R1 began to decrease and at 72th hour the level of IL-10R1 was similar with the level at 0th hour.Conclusion:The expression of IL-10R1 on activated CD4+T cell is short in mice,with peak in 24 hours.
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2011年第12期1101-1103,共3页 Chinese Journal of Immunology
基金 沈阳医学院青年基金项目(No.20092016)
关键词 T淋巴细胞 白细胞介素10 白细胞介素10受体 免疫调节 T lymphocyte Interleukin 10 Interleukin 10 receptor Immunity regulation
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参考文献8

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同被引文献24

  • 1李丽,祁赞梅,李艳秋,陈洋,都殊研,姜奕.系统性红斑狼疮抗核抗体易感基因染色体定位[J].中国免疫学杂志,2004,20(9):610-613. 被引量:5
  • 2Sun KH, Yu CL, Tang SJ, et al. Monoclonal anti-double-stran- ded DNA autoantibody stimulates the expression and release of IL- lbeta, IL-6, IL-8, IL-10 and TNF-alpha from normal human no- nuclear cells involving in the lupus pathogenesis [ J ]. Immunolo- gy, 2000, 99 (3): 352-360.
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  • 4Heo YJ, Joo YB, Oh HJ, etal. IL-10 suppresses Thl7 cells and promotes regulatory T ceils in the CD4 * T cell population of rheu- matoid arthritis patients [J]. Immunol Lett, 2010, 127 (2): 150 - 156.
  • 5Liu Y, Wei SH, Ho AS, et al. Expression cloning and charac- terization of a human IL-10 receptor [J]. J Immunol, 1994, 152(4) : 1821 - 1829.
  • 6Spencer SD, Di Marco F, Hooley J, et al. The orphan receptor CRF2-4 is an essential subunit of the interleukin 10 receptor [ J]. J Exp Med, 1998, 187 (4) : 571-578.
  • 7Qi ZM, Wang J, Sun ZR, et al. Polymorphism of the moue gene for the interleukin 10 receptor alpha chain (IL-10Ra) and its asso- ciation with the autoimmune phenotype [ J ]. Immunogenetics, 2005, 57 (9): 697-702.
  • 8Biswas PS, Pedicord V, Ploss A, et al. Pathogen-Specific CD8 T Cell Responses Are Directly Inhibited by IL-10 [ J ]. J Immunol, 2007, 179 (7): 4520-4528.
  • 9Xu Y,Chen ZQ, Li YM, et al. Correlation between some Thl and Th2 cytokin e receptor gene polymorphisms and systemic lu- pus erythematosus in Chinese patients [ J ]. Int J Dermatol, 2007. 46 (11): 1129-1135.
  • 10Valencia-Pacheeo G, Layseca-Espinosa E, Nino-Moreno P, et al. Expression and function of IL-10R in mononuclear cells from patients with systemic lupus erythe matosus [ J ]. Scand J Rheu- matol, 2006, 35 (5): 368-378.

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