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TF3-H4对CD4~+CD25~+调节性T细胞和CD4~+CD25~-效应性T细胞早期活化的影响
引用本文:李晓娟,胡义平,刘燕,姜志宏,刘叔文. TF3-H4对CD4~+CD25~+调节性T细胞和CD4~+CD25~-效应性T细胞早期活化的影响[J]. 中国药理学通报, 2012, 28(3): 371-374
作者姓名:李晓娟  胡义平  刘燕  姜志宏  刘叔文
作者单位:1. 南方医科大学药学院,广东,广州,510515
2. 澳门科技大学中药质量控制国家重点实验室,澳门
基金项目:国家自然科学基金资助项目
摘    要:目的观察1',2',3',7'-四氢茶黄素-3,3'-双没食子酸酯(TF3-H4)对CD4+CD25+调节性T细胞和CD4+CD25-效应性T细胞早期活化的影响,分析TF3-H4对两群功能相反的CD4+T细胞的作用。方法免疫磁珠分离BALB/c小鼠脾脏CD4+CD25+调节性T细胞和CD4+CD25-效应性T细胞,加入ConA或PDB,和TF3-H4共同孵育12 h后收集细胞,流式细胞仪分析细胞表面早期活化标志CD69的表达。结果在ConA和PDB的作用下,两群细胞早期活化标志CD69的表达均升高。TF3-H4(20 mg.L-1)不能抑制PKC激动剂PDB激活的CD4+CD25-效应性T细胞CD69的表达,却能抑制ConA激活的CD4+CD25-效应性T细胞CD69表达;同时,TF3-H4也能明显抑制ConA激活的CD4+CD25+调节性T细胞的CD69表达。结论茶黄素衍生物TF3-H4可能经由TCR活化途径的上游抑制CD4+CD25-效应性T细胞活化;TF3-H4对CD4+CD25+调节性T细胞和CD4+CD25-效应性T细胞早期活化的抑制作用,可能是该类化合物发挥抗炎、抗肿瘤作用的机制之一。

关 键 词:CD4+CD25+调节性T细胞  TF3-H4  CD69  免疫活化  茶黄素  CD4+CD25-效应性T细胞

Effects of TF3-H4 on the early activation of CD4~+CD25~+ Treg cells and CD4~+CD25~-Teff cells in mice by flow cytometry
LI Xiao-juan , HU Yi-ping , LIU Yan , JIANG Zhi-hong , LIU Shu-wen. Effects of TF3-H4 on the early activation of CD4~+CD25~+ Treg cells and CD4~+CD25~-Teff cells in mice by flow cytometry[J]. Chinese Pharmacological Bulletin, 2012, 28(3): 371-374
Authors:LI Xiao-juan    HU Yi-ping    LIU Yan    JIANG Zhi-hong    LIU Shu-wen
Affiliation:1(1.School of Pharmaceutical Sciences,Southern Medical University,Guangzhou 510515,China;2.State Key Laboratoryfor Quality Research in Chinese Medicines,Macau University of Science and Technology,Macau,China)
Abstract:Aim To study the effects of theaflavin derivative compound,1′,2′,3′,7′-4H-Theaflavin-3,3′-digallate(TF3-H4),on the early activation of CD4+CD25+ regulatory T cells and CD4+CD25-effector T cells,and evaluate the effects of TF3-H4 on two groups of CD4+T cells with opposite functions.Methods The CD4+CD25+ regulatory T cells and CD4+CD25-effector T cells of BALB/c mice were separated by MACS immunomagnetic beads.After 12 hours of stimulation with ConA or PDB with or without the presence of TF3-H4,the cells were collected and the percentage of CD69 expression was analyzed by flow cytometry.Results Both ConA and PDB could increase CD69 expression of CD4+CD25+ regulatory T cells and CD4+CD25-effector T cells.TF3-H4 at 20 mg·L-1 could decrease CD69 expression of CD4+CD25-effector T cells stimulated by ConA,but had no effect on CD69 expression of CD4+CD25-effector T cells stimulated by PDB.Moreover,CD69 expression of CD4+CD25+ regulatory T cells stimulated by ConA was also suppressed significantly by TF3-H4.Conclusions The activation of CD4+CD25-effector T cells in vitro might be inhibited by TF3-H4 through the upstream pathway of TCR.The inhibitory function of TF3-H4 on the early activation of CD4+CD25+ regulatory T cells and CD4+CD25-effector T cells may contribute to its anti-inflammation and anti-tumor effects.
Keywords:CD4+CD25+ regulatory T cells  TF3-H4  CD69  immunoactivation  Theaflavin  CD4+CD25-effector T cells
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