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CD4^+CD25^+调节性T细胞在α-GalCer预防T1D中的作用机制探讨

The Role of CD4^+CD25^+T Regulatory Cells in Preventing the Development of T1D in α-Gal Cer Cer-treated NOD Mice
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摘要 目的:研究CD4+CD25+调节性T细胞在α-GalCer预防NOD小鼠T1D中的作用机制。方法:流式细胞仪分析反复注射α-GalCer的NOD小鼠胰腺引流淋巴结(PLN)CD4+CD25+T细胞频率,CD4+CD25+T细胞中FoxP3+细胞的比例,CD4+CD25+FoxP3+T细胞的FoxP3平均荧光强度(MFI);检测CD4+CD25+调节性T细胞的抑制功能。用Anti-CD25阻断CD4+CD25+调节性T细胞的功能。结果:α-GalCer处理过的小鼠的CD4+CD25+T细胞中FoxP3+细胞的比例增加,CD4+CD25+FoxP3+T细胞的FoxP3平均荧光强度(MFI)增强,CD4+CD25+Treg细胞的抑制功能增强。采用CD4+CD25+调节性T细胞功能阻断剂后,α-GalCer不能预防T1D的发生。结论:CD4+CD25+调节性T细胞在α-GalCer预防NOD小鼠T1D中数量增加、功能增强,且是必需的。 Objective To investigate the role that CD4+CD25+T regulatory(CD4+CD25+Treg) cells played in preventing the development of typeⅠ diabetes(T1D) in α-GalCer-treated NOD mice.Methods The frequency of CD4^+CD25^+T cell from pancreatic lymph node(PLN) was analysed,the percentages of CD4^+CD25^+T cells expressing FoxP3 were observed,mean fluorescent intensity(MFI) of FoxP3 in CD4^+CD25^+ FoxP3^+T cells was assayed in vitro.In vivo suppression experiment of CD4^+CD25^+Treg cells with anti-CD25^+ was performed.Results Both the percentages of CD4^+ CD25^+T cells experssing FoxP3 and the mean fluorescent intensity(MFI) of FoxP3 in CD4^+CD25^+ FoxP3^+T cells were increased after α-GalCer treatment.With in vitro suppression assay,CD4^+CD25^+Treg cells showed increased ability to suppress the proliferation of CD4^+CD25^+T cells.In vivo suppression experiment showed that α-GalCer could not prevent the development of T1D in NOD mice after suppression of CD4^+CD25^+Treg cells.Conclusion CD4^+CD25^+Treg cells played an import.ant role in the prevention of the development of T1D in α-GalCer-treated NOD mice.
出处 《放射免疫学杂志》 CAS 2009年第5期513-516,共4页 Journal of Radioimmanology
关键词 CD4+CD25+调节性T细胞 平均荧光强度 转录因子FOXP3 环磷酰胺 Α-GALCER CD4+CD25+T regulatory cells mean fluorescent intensity transcription fator FoxP3 CY α-GalCer
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参考文献14

  • 1李卫鹏,申勇,胡永全,史桂英,王福庆.NOD小鼠CD4^+CD25^+调节性T细胞功能变化研究[J].蚌埠医学院学报,2008,33(6):743-746. 被引量:2
  • 2Hong S, Wilson MT, Serizawa I, et al. The natural killer T--cell lig- and alpha-galactosylceramide prevents autoimmune diabetes in non-obese diabetic mice[J]. Nat Med, 2001,7(9) :1052-1056.
  • 3Sharif S, Arreaza GA, Zucker P, et al. Activation of natural killer T cells by alpha-galactesylccramide treatment prevents the onset and recurrence of antoimmune Type 1 dlabetes[J]. Nat Med, 2001,7(9) :1057- 1062.
  • 4Fontenot JD, Gavin MA and Ruder.sky AY. FoxP3 programs the development and function of CD4 ^+ CD25 ^+ regulatory T cells[J]. Nat Immunol, 2003, 4(4) :330-336.
  • 5Khattri R, Cox T, Yasayko SA, et al. An essential role for scurfin in CD4 ^+ CD25^+ Tregulatory cells[ J]. Nat Immunol, 2003,4(4) :337-342.
  • 6Hori S, Nomura T and Sakaguchi S. Control of regulatory T cell development by the transcription factor FoxP3 [J ]. Science, 2003,299 (5609) : 1057 -1061.
  • 7Kawano T, Cui J, Koezuka Y, et al. CDld-restricted and TCR-mediated activation of valpha 14 NKT cells by glycosylceramides[J]. Science, 1997,278 (5343) : 1626-1629.
  • 8Kitamura H, Iwakabe K, Yahata T, et al. The natural killex T (NKT) cell ligand alpha-galactosylceramide dcmonstratesits immunopotentiating effect by inducing interlcukin (IL) -12 production by dendritic cells and IL-12 receptor expression on NK T cells[J]. J Exp Med, 1999, 189(7) :1121-1128.
  • 9LY D, Mi QS, Hussain S, et al. Protection from type 1 diabetes by invariant NKT cells requires the activity of CD4 ^+ CD25^ + regulatory T cells [J]. J Immunol, 2006,177(6) :3695-3704.
  • 10Jiang S, Game DS, Davies D, et al. Activated CD1d-restrieted natural killer T ceils secrete IL-2 : innate help for CD4^ + CD25 ^+ regulatory T cells? [J]. EurJ Immunol, 2005,35(4) :1193-1200.

二级参考文献10

  • 1Sakaguchi S, Sakaguehi N, Asano M, et al. Immunologic self- tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains ( CD25 ). Breakdown of a single mechanism of self- tolerance causes various autoimmune diseases [ J]. J Immunol, 1995,155(3) :1 151 -1 564.
  • 2Banham AH. Cell-surface IL-7 receptor expression facilitates the purification of FOXP3 ( + ) regulatory T cells [ J ]. Trends Immunol,2006,27 ( 12 ) :541 - 544.
  • 3Bruder D,Probst-Kepper M,Westendorf AM, et al. Neuropilin-1 : a surface marker of regulatory T cells[ J]. Eur J Immunol,2004, 34 (3) :623 - 630.
  • 4Fehervari Z, Sakaguchi S. Development and function of CD25^+ CD4^+ regulatory T cells [ J ]. Curr Opin Immunol, 2004,16 ( 2 ) : 203 - 208.
  • 5Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4^+ CD25^+ regulatory T cells[J]. Nat Immunol,2003 ,4( 4 ) :330 -336.
  • 6Khattri R, Cox T, Yasayko SA, et al. An essential role for Scurfin in CD4^+CD2^+ T regulatory cells4 [ J ]. Nat Immunol, 2003,4 (4) :337 -342.
  • 7Hori S, Nomura T, Sakaguchi S. Control of regulatory T cell development by the transcription factor Foxp3 [ J ]. Science,2003, 14 299(5 609) :1 057 -1 061.
  • 8Ono M, Yaguchi H, Ohkura N,et al. Foxp3 controls regulatory T- cell function by interacting with AML1/Runx1 [ J ]. Nature,2007, 446(7 136) :685 -689.
  • 9Oh U, Grant C, Griffith C, et al. Reduced Foxp3 protein expression is assoeiated with inflammatory disease during human t lymphotropic virus type 1 Infection [ J ]. J Infect Dis,2006,193 (11) :1 557-1 566.
  • 10Read S, Greenwald R, Izcue A, et al. Blockade of CTLA-4 on CD4^+ CD25^+ regulatory T cells abrogates their function in vivo [J]. J Immunol,2006,177(7) :4 376 -4 383.

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