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CD3TCR复合物抗体诱导不成熟胸腺细胞亚群的凋亡

Apoptosis effect of induced by antibodies to CD3/TCR complex in immature T cells

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【作者】 李红梅王宏程张华刚孔宪涛陈慰峰

【Author】 LI Hong Mei *,WANG Hong Cheng *,ZHANG Hua Gang * et al Department of Clinical Laboratory,Changzheng Hospital,Second Military Medical University, Shanghai 200003,China.*Key Laboratory of Medical Immunology,Ministry of Health in China,Beijing Medical University,Beijing 100083,China.

【机构】 北京大学医学部免疫系卫生部医学免疫学重点实验室上海长征医院临床实验科北京大学医学部免疫系卫生部医学免疫学重点实验室 北京100083北京100083上海200003北京100083

【摘要】 目的 :采用AnnexinV ,PI染色 ,流式细胞仪分析的方法、DNA琼脂糖电泳法检测不同CD3 TCR复合物抗体对小鼠胸腺T淋巴细胞亚群的促凋亡作用。方法 :新鲜分离胸腺细胞 ,加入PMA、anti TCR +anti CD2 8mAb ,anti TCRmAb等培养 2 0小时 ,AnnexinV ,PI ,CD4 ,CD8细胞染色以及TCR三染 ,进行FACS分析 ,同时抽提培养细胞DNA进行琼脂糖电泳。结果 :PMA +IONO诱导胸腺T细胞的凋亡作用最强 ,anti TCR +anti CD2 8mAb次之 ,anti TCRmAb最弱。结论 :AnnexinV ,PI细胞染色 ,流式细胞仪分析的方法可以灵敏检测T淋巴细胞的凋亡 ;anti TCR +anti CD2 8mAb能明显增强anti TCRmAb促不成熟的CD4 + CD8+TCR+ 和CD4 + TCR+ 细胞的凋亡作用 ;不成熟T细胞经TCR与自身抗原结合的活性过程能产生克隆删除从而产生自我耐受。

【Abstract】 Objective:To investigate the apoptosis induced by antibodies to CD3/TCR complex in immature T cells, lymphocytes were labelled with AnnexinV,PI,then analyzed by flow cytometry and DNA were extracted agarose electrophoresis Methods:Fresh thymocytes and lymph node cells were separated, then the cells were cultured with the addition of PMA?anti TCRαβ+ anti CD28 mAb and anti TCRαβ up to 20 h, stained with AnnexinV,PI; CD8 FITC,CD4 PE,TCR APC,the data were collected through FACS analysis ; DNA was isolated from cultured thymocytes, and analyzed through agarose electrophoresis Results:Effects of different stimulators on the apoptosis of thymocytes are different PMA plus IONO is the most intensive stimulators in thymocyte apoptosis, anti TCRαβ is the weakest Conclusion:The method that FACS analysis in combines with AnnexinV,PI staining permits the detection of apoptosis cells at sensitive level; anti TCRαβ+ anti CD28 mAb induces significant apoptosis of immature CD4 +CD8 +TCR + and semimature CD4 +TCR + thymocytes than anti TCRαβ mAb alone;Activation of this process in immature T cells by the binding of the TCR to self antigens may therefore be the mechanism which produces clonal deletion and consequently self tolerance

【基金】 国家自然科学基金 ( 3 973 0 410 )资助
  • 【文献出处】 中国免疫学杂志 ,Chinese Journal of Immunology , 编辑部邮箱 ,2003年04期
  • 【分类号】R392
  • 【下载频次】89
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