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AA和MDS患者骨髓CD+34细胞表面GM-CSFR的表达及意义
引用本文:于媛,许洪志,李英,李爱,徐功立. AA和MDS患者骨髓CD+34细胞表面GM-CSFR的表达及意义[J]. 山东医药, 2006, 46(16): 1-2
作者姓名:于媛  许洪志  李英  李爱  徐功立
作者单位:山东省立医院,山东,济南,250021;山东省立医院,山东,济南,250021;山东省立医院,山东,济南,250021;山东省立医院,山东,济南,250021;山东省立医院,山东,济南,250021
基金项目:山东省医药卫生科技发展计划(HW116).
摘    要:
目的 探讨再生障碍性贫血(AA)和骨髓增生异常综合征(MDS)患者骨髓CD34^+细胞表面粒细胞-巨噬细胞集落刺激因子受体(GM—CSFR)的表达情况。方法 用流式细胞术(FCM)和单克隆抗体技术检测14例AA、23例MDS和8例非血液病患者骨髓CD34^+细胞表面的GM—CSFR表达率。结果 MDS组骨髓CD34^+细胞表面GM-CSFR的表达率明显高于对照组及AA组(P〈O.05),而AA组与对照组间差异无统计学意义(P〉0.05)。结论 AA患者造血干细胞没有质的缺陷;造血干细胞异常可能是MDS的主要发病机制之一。

关 键 词:贫血  再生障碍性  骨髓增生异常综合征  抗原  CD34  粒细胞巨噬细胞集落刺激因子  受体  集落刺激因子
文章编号:1002-266X(2006)16-0001-02
收稿时间:2006-04-19
修稿时间:2006-04-19

Expression and value of GM-CSF receptors on CD34 positive cells in bone marrow of patients with aplastic and myelodysplastic syndrome
YU Yuan, XU Hong-zhi, LI Ying, et al. Expression and value of GM-CSF receptors on CD34 positive cells in bone marrow of patients with aplastic and myelodysplastic syndrome[J]. Shandong Medical Journal, 2006, 46(16): 1-2
Authors:YU Yuan   XU Hong-zhi   LI Ying   et al
Abstract:
[Objective] To detect expression rate of granulocytemacrophage colony-stimulating factor receptors(GM-CSFR) on CD_(34) positive cells in bone marrow of patients with aplastic anemia(AA) and myelodysplastic syndrome(MDS).[Methods] The expression rates of GM-CSFR on CD_(34) positive cells in 14 AA patients, 23 MDS patients and 8 normal cases were detected by flow cytometry(FCM) and monoclonal antibody technique.[Results] The expression rate of GM-CSFR on CD_(34) positive cells in MDS group was higher than that in control group and AA group(P<0.05).There was no significant difference between AA group and control group(P>0.05).[Conclusion] It suggests that the quality of hematopoietic stem cells is normal in AA and the damaged quality of hematopoietic stem cells is one of the principal pathogenesis in MDS.
Keywords:anemia, aplastic    myelodysplastic syndromes    antigens, CD34    granulocyte-macrophage colonystimulating factor   receptors, colony-stimulating factor
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