首页> 外文期刊>Journal of hematotherapy and stem cell research >Quantitative expression of adhesion molecules on granulocyte colony-stimulating factor-mobilized peripheral blood, bone marrow, and cord blood CD34+ cells.
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Quantitative expression of adhesion molecules on granulocyte colony-stimulating factor-mobilized peripheral blood, bone marrow, and cord blood CD34+ cells.

机译:粘附分子在粒细胞集落刺激因子动员的外周血,骨髓和脐带血CD34 +细胞上的定量表达。

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The purpose of this study is to investigate the function of the main adhesion receptors on CD34(+) cells during hematopoietic stem cell transplantation. Expression was quantified by flow cytometry using calibration beads. CD34(+) cells were isolated from either bone marrow (BM), cord blood (CB), or peripheral blood (PB) from study patients and a control group after granulocyte colony-stimulating factor (G-CSF) administration. The study of the CD34(+) cell differentiation showed that CD34(+) cells are mainly CD38(+) and HLA-DR(+), whatever the type of harvest. However, quantitative analysis elicited a weaker expression of CD38 on PB and CB CD34(+) cells in comparison to BM CD34(+) cells. The proportions of CD34(+)/CD49d(+) and CD34(+)/CD49e(+) were smaller on PB cells, without quantitative expression variation. This phenotypic variation promotes CD34(+) cells to exit from BM into circulation, inducing the mobilization. The homing of the CD34(+) cells to the BM involves the CD62L receptor. The expressionof this receptor was found to be more frequent and stronger on PB cells than on BM or CB cells. The CD11b, CD18, and CD54 receptors are implicated in CD34(+) cell adhesion to BM microenvironment. No significant variation in CD34(+)/CD11b(+) and CD34(+)/CD18(+) cell frequency was noted. Moreover, the CD54 receptor was more frequently expressed on CB and PB cells. Quantitative analysis revealed that CD18 was more strongly expressed on BM than on PB cells to promote progenitors adhesion by interacting with stromal cells. Finally, the quantitative expression of the main receptors on CD34(+) cells explained cellular functions during the different steps of hematopoietic stem cells transplantation.
机译:这项研究的目的是调查造血干细胞移植过程中CD34(+)细胞上主要粘附受体的功能。使用校准珠通过流式细胞术定量表达。给予粒细胞集落刺激因子(G-CSF)后,从研究患者和对照组的骨髓(BM),脐带血(CB)或外周血(PB)中分离出CD34(+)细胞。 CD34(+)细胞分化的研究表明,无论收获的类型如何,CD34(+)细胞主要是CD38(+)和HLA-DR(+)。但是,定量分析引发与BM CD34(+)细胞相比,PB和CB CD34(+)细胞上CD38的表达较弱。 PB细胞上CD34(+)/ CD49d(+)和CD34(+)/ CD49e(+)的比例较小,没有定量表达变化。这种表型变异促进CD34(+)细胞从BM进入循环系统,从而引起动员。 CD34(+)细胞归巢到BM涉及CD62L受体。发现该受体在PB细胞上的表达比在BM或CB细胞上更频繁和更强。 CD11b,CD18和CD54受体与CD34(+)细胞对BM微环境的粘附有关。没有观察到CD34(+)/ CD11b(+)和CD34(+)/ CD18(+)细胞频率的显着变化。而且,CD54受体在CB和PB细胞上更频繁地表达。定量分析表明,CD18在BM上的表达要强于PB细胞,以通过与基质细胞相互作用来促进祖细胞粘附。最后,CD34(+)细胞上主要受体的定量表达解释了造血干细胞移植不同步骤中的细胞功能。

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