NOD小鼠CD4+CD25+调节性T细胞功能变化研究

    Changes of function of CD4+CD25+ T regulatory cells in NOD mice

    • 摘要: 目的:观察NOD小鼠CD4+CD25+调节性T细胞的功能变化。方法:流式细胞仪分析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。结果:在不同的年龄阶段,CD4+CD25+调节性T细胞数量未发生明显变化,而随时间的推移,CD4+CD25+调节性T细胞中FoxP3表达水平降低,CD4+CD25+调节性T细胞的功能也下降。结论:CD4+CD25+调节性T细胞的抑制功能降低可能是NOD小鼠糖尿病发作的根本原因。

       

      Abstract: Objective: To investigate the function of CD4+CD25+ T regulatory(CD4+CD25+ Treg) cells in NOD mice.Methods: The frequency of CD4+CD25+ T cells from pancreatic lympho node(PLN) was analysed,the percentages change over time in the proportion of NOD CD4+ CD25+ T cells expressing Foxp3 were observed,mean fluorescent intensity(MFI) of Foxp3 in CD4+ CD25+ FoxP3+ T cells was assayed,and in vitro suppression assay was performed.Results: No percentages change over time in the proportion of NOD CD4+ CD25+ T cells expressing Foxp3 were observed.But the mean fluorescent intensity(MFI) of Foxp3 in CD4+CD25+FoxP3+ T cells decreased with time.In vitro suppression assay,PLN CD4+CD25+ T cells show decrease in their ability to suppress the proliferation of CD4+CD25- T cells.There exists some relationship between the impairment of in vitro suppression and the reduction at the protein expression levels of Foxp3 on a per-cell basis.Conclusions: It is the impairment of the function of CD4+CD25+ Treg cells that results in the development of diabetes mellitus in NOD mice.

       

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