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CD28协同刺激分子对T细胞受体介导的胸腺细胞亚群凋亡的影响
引用本文:李红梅,张华刚,王宏程,钱晓萍,孔宪涛,陈慰峰.CD28协同刺激分子对T细胞受体介导的胸腺细胞亚群凋亡的影响[J].细胞与分子免疫学杂志,2003,19(1):14-16.
作者姓名:李红梅  张华刚  王宏程  钱晓萍  孔宪涛  陈慰峰
作者单位:1. 北京大学医学部免疫学系,北京,100083;第二军医大学长征医院临床实验科,上海,200003
2. 北京大学医学部免疫学系,北京,100083
3. 第二军医大学长征医院临床实验科,上海,200003
基金项目:国家自然科学基金资助(No.39730410)
摘    要:目的:分析anti-TCRαβmAb anti-CD28mAb诱导小鼠胸腺淋巴细胞不同亚群的凋亡及凋亡程度,分析CD28协同刺激分子对TCR受体介导的胸腺细胞亚群凋亡的影响。方法:新鲜分离胸腺细胞,加入anti-TCRαβmAb-anti-TCRαβmAb anti-CD28mAb等培养20h,进行多重染色,流式细胞仪分析。结果:与胸腺细胞自发凋亡的结果相比较;(1)双信号刺激可明显增加胸腺细胞凋亡的数目,尤其是CD4^ CD8^ 胸腺细胞的凋亡数目。(2)凋亡的CD4^ CD8^ 亚群,CD4^ CD8^-亚群细胞表面CD28的表达均增多。结论:CD28共刺激分子对TCR受体介导的胸腺细胞亚群凋亡的影响与细胞的成熟程度有关,CD28共刺激分子能明显增强不成熟皮质胸腺细胞的凋亡。

关 键 词:CD28协同刺激分子  T细胞受体介导  胸腺细胞亚群  细胞凋亡
文章编号:1007-8738(2003)01-014-03
修稿时间:2002年6月17日

Effect of CD28 costimulator on T Cell receptor(TCR)-induced apoptosis of thymocytes
LI Hong-mei,ZHANG Hua-gang,WANG Hong-cheng,QIAN Xiao-ping,KONG Xian-tao,CHEN Wei-feng Depertment of Immunology,Peking University Health Science Center,Beijing ,China.Effect of CD28 costimulator on T Cell receptor(TCR)-induced apoptosis of thymocytes[J].Journal of Cellular and Molecular Immunology,2003,19(1):14-16.
Authors:LI Hong-mei  ZHANG Hua-gang  WANG Hong-cheng  QIAN Xiao-ping  KONG Xian-tao  CHEN Wei-feng Depertment of Immunology  Peking University Health Science Center  Beijing  China
Institution:Department of Immunology, Peking University Health Science Center, Beijing 100083, China.
Abstract:AIM: To analyze apoptosis and its degree of thymocytes at early and intermediate phases induced by anti-TCRalphabeta mAb or anti-TCRalphabeta mAb+anti-CD28 mAb stimuli, and to analyze the influence of CD28 costimulator on TCR-induced apoptosis of thymocyte subsets. METHODS: Thymocytes were freshly prepared and were cultured for 20 h in the presence of anti-TCRalphabeta mAb+anti-CD28 mAb or anti-TCRalphabeta mAb along, The cultured cells were stained with fluorescein labelled Annexin V, PI, anti-CD4 mAb and anti-CD8 mAb, then color reagents. The apoptotic cells were analyzed by FACS. RESULTS: Compared with the spontaneous apoptosis of thymocytes cultured in medium alone, CD28 costimulator markedly enhanced the number of thymocyte apoptosis at early and intermediate phases; under the action of double signaling stimulators, the apoptosis of CD4(+) CD8(+)(DP) thymocytes were substantially increased, and the expression of CD28 were also upregulated on these apoptotic DP cells. CONCLUSION: Influence of CD28 costimulator on TCR-induced apoptosis of thymocyte subsets might be related to thymocyte's mature degree. Double signaling may induce apoptosis of DP thymocytes.
Keywords:CD28 costimulator  T cell receptor  thymocyte subsets  apoptosis
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