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