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电子期刊 >> 正文 |
摘要:
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目的:探讨TNF-α和Fas/FasL的表达及骨髓细胞凋亡与骨髓增生异常综合征(myelodysplastic syndrome,MDS)发生发展的关系.方法:采用ELISA法检测MDS患者骨髓单个核细胞培养上清液中TNF-α浓度,采用流式细胞术测定骨髓CD 34+细胞Fas、FasL的表达率和细胞凋亡率.结果:各型MDS患者骨髓单个核细胞培养上清液中TNF-α浓度和CD 34+细胞Fas、FasL的表达率均明显高于正常对照组(P<0.01).其中RA/RAS组的TNF-α浓度和CD 34+细胞Fas+表达率均明显高于RAEB和RAEB-t组(P<0.001),而RAEB与RAEB-t组组间无明显差异(P值分别为0.115和0.239);RAEB和RAEB-t组细胞的CD 34+FasL+表达率明显高于RA/RAS组(P值分别为0.001和0.010).RA/RAS和RAEB组的细胞凋亡率均高于对照组(P值均为0.000),而RAEB-t组的细胞凋亡率与对照组相近(P=0.216).各型MDS患者TNF-α浓度与CD34+Fas+表达率呈正相关(r=0.570,P=0.012).而CD 34+细胞凋亡率与TNF-α浓度或CD 34+Fas+表达率之间均无直线相关关系(P值分别为0.103和0.091).结论:MDS患者骨髓细胞的凋亡受多因素的调节,TNF-α与Fas/FasL系统介导的凋亡以及机体对其调控的失常参与了MDS骨髓无效造血的病理生理过程.
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