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再生障碍性贫血患者骨髓CD34~+和Fas~+细胞Fas抗原的表达
引用本文:万岁桂,孙雪静,刘聪艳,赵弘,徐娟,田丁. 再生障碍性贫血患者骨髓CD34~+和Fas~+细胞Fas抗原的表达[J]. 首都医科大学学报, 2002, 23(2): 128-130
作者姓名:万岁桂  孙雪静  刘聪艳  赵弘  徐娟  田丁
作者单位:首都医科大学宣武医院血液科(万岁桂,孙雪静,刘聪艳,赵弘,徐娟),首都医科大学宣武医院血液科(田丁)
基金项目:北京市科干局基金资助项目
摘    要:采用流式细胞术检测再生障碍性贫血 (AA ,以下简称再障 )患者骨髓CD34 + 细胞表面Fas抗原的表达 ,采用体外短期液体培养的方法研究干扰素γ(IFN γ)对AA患者骨髓CD34 + 细胞表面Fas抗原表达的影响 ,以探讨Fas介导的凋亡在AA发病中的作用。正常对照骨髓CD34 + 细胞表面Fas抗原的表达率为 ( 1 0 .0 2± 2 .33) % ,重型再障组(SAA)和慢性再障组 (CAA)分别为 ( 38.2 8± 9.0 1 ) %和 ( 2 6 .6 6± 4 .2 7) % ,SAA组和CAA组与对照组比较均有显著性差异 (P <0 .0 1 ,P <0 .0 5 ) ;SAA组与CAA组比较也有显著性差异 (P <0 .0 5 )。正常骨髓单个核细胞在含SCF、IL 3、GM SCF和EPO细胞因子组合的液体培养体系中培养 ,加入IFN γ时 ,CD34 + 细胞表面Fas抗原表达稍增高 ,AA患者骨髓在上述相同的条件下 ,CD34 + 细胞表面Fas抗原表达与正常对照骨髓比较显著增高 (P <0 .0 5 ) ,且SAA组明显高于CAA组 (P <0 .0 5 )。实验结果表明 ,AA患者骨髓CD34 + 细胞表面Fas的表达明显高于正常对照 ;AA患者骨髓单个核细胞体外培养时 ,IFN γ促使骨髓CD34 + 细胞表面Fas的表达作用较正常对照明显增强。结果提示 ,AA患者骨髓CD34 + 细胞表面Fas的异常表达可能与AA的发病有关。

关 键 词:贫血  再生障碍性  CD95  干扰素γ  细胞凋亡
收稿时间:2001-12-19
修稿时间:2001-12-19

Expression of Fas Antigen on Bone Marrow CD34+ Cells in Patients with Aplastic Anemia
Wan Suigui,Sun Xuejing,Liu Congyan,Zhao Hong,Xu Juan,Tian Ding. Expression of Fas Antigen on Bone Marrow CD34+ Cells in Patients with Aplastic Anemia[J]. Journal of Capital Medical University, 2002, 23(2): 128-130
Authors:Wan Suigui  Sun Xuejing  Liu Congyan  Zhao Hong  Xu Juan  Tian Ding
Affiliation:Wan Suigui,Sun Xuejing,Liu Congyan,Zhao Hong,Xu Juan,Tian Ding Department of Hematology,Beijing Xuanwu Hospital,Affiliate of Capital University of Medical Sciences
Abstract:The objective of the study was to investigate Fas antigen induced apoptosis in the pathogenesis of aplastic anemia. The expression of Fas antigen on bone marrow CD34+ cells and the effect of IFN-γ to it were assayed in AA by flowing cytometry and short-liquid-culture in vitro. Fas antigen expression on CD34+ cells in SAA and CAA was significantly higher than that in normal controls 〔(38.28± 9.01)% and(26.66±4.27)% vs(10.02±2.33)%, (P<0.01, (P<0.05 respectly〕. Fas antigen expression on CD34+ cells in CAA was significantly lower than that in SAA(P<0.05). Addition of IFN-γ to liquid culture of BMMNC including SCF, IL-3, GM-CSF and EPO cytokines showed significant stimulating effects on Fas antigen expression in AA, but not in normal controls, the expression in SAA was higher than that in CAA(P<0.05). The abnormal expression of Fas antigen on CD34+ cells may be involved in the pathogenesis of AA.
Keywords:CD95
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