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PDCD4基因对T淋巴细胞亚群分化的影响 被引量:1

The influence of PDCD4 gene to the differentiation of T lymphocytes subsets
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摘要 目的探讨PDCD4基因对小鼠T淋巴细胞亚群分化的影响。方法采用流式细胞术检测PDCD4基因缺失小鼠脾细胞和淋巴结细胞中的CD8+T和CD4+T,及其亚群Th1、Th2、Th17和调节性T细胞(Treg)的特异性标记分子,并分析各细胞亚群的比例变化。结果 pdcd4-/-小鼠脾脏和淋巴结中CD8+T细胞数量较野生型C57BL/6小鼠有所下降(P<0.05),CD4+T细胞及Th1细胞也呈下降趋势,差异无统计学意义(P>0.05);而PDCD4基因缺失后Th2和Th17的分化比例无显著变化(P>0.05);进一步分析CD4+T细胞群体中CD25+Foxp3+Treg的表达,发现pdcd4-/-小鼠CD25+Foxp3+Treg比例明显上调(P<0.05)。结论 PDCD4基因能够影响部分T淋巴细胞亚群的分化,PDCD4基因敲除小鼠中CD8+T细胞数量下降和CD25+Foxp3+Treg比例升高,提示PDCD4基因有可能在免疫调节方面起到一定作用。而PDCD4基因对于CD4+T以及Th1、Th2和Th17的分化并无明显作用。 Objective To investigate the influence of PDCD4 gene to the differentiation of T lymphocyte subsets.Methods Detect the expression differences of CD8+T,CD4+T and its subsets such as Th1、Th2,Th17 and CD25+Foxp3+Treg in the splenocytes and lymph nodes of pdcd4-/-mice and C57BL/6 mice by flow cytometry.And analyse the ratio change of the lymphocyte subsets.Results Compared with that of the C57BL/6 mice,the number of CD8+T cells decreased in the pdcd4-/-mice(P0.05).CD4+T and Th1 cells also showed a descending tendency but had no statistic significance(P0.05).The proportion of CD4+CD25+Foxp3+Treg significantly increased in the pdcd4-/-mice(P0.05).Conclusion PDCD4 can influence the differentiation of partial T lymphocyte subsets,the low expression of CD8+T cells as well as high proportion of CD4+CD25+Foxp3+Treg in the pdcd4-/-mice suggest that PDCD4 gene may play a role in the immune regulation.However,PDCD4 gene has no significant influence on the differentiation of CD4+T and Th1、Th2 and Th17 cells.
出处 《山东大学学报(医学版)》 CAS 北大核心 2012年第11期6-10,17,共6页 Journal of Shandong University:Health Sciences
基金 国家自然科学基金(81172863)
关键词 PDCD4基因 脾脏 淋巴结 CD4+T细胞 CD8+T细胞 TH1细胞 TH2细胞 Th17细胞 CD25+Foxp3+Treg PDCD4 gene Splenocyte Lymph node CD4+T cells CD8+T cells Th1 cells Th2 cells Th17 cells CD25+Foxp3+Treg
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参考文献4

  • 1Gao F, Zhang P, Zhang L N, et al. Frequent loss of Pd- cd4 expression in human glioma: Possible role in the tu- morigenesis of glioma[J].Oncol Rep, 2007, 17 ( 1 ) : 123-128.
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