Carion Alexandra, Domenech Jorge, Hérault Olivier, Benboubker Lotfi, Clément Nathalie, Bernard Marie-Christine, Desbois Isabelle, Colombat Philippe, Binet Christian
Laboratory of Hematology, University Hospital of Tours, France.
J Hematother Stem Cell Res. 2002 Jun;11(3):491-500. doi: 10.1089/15258160260090951.
Molecular mechanisms leading to mobilization of hematopoietic cells from bone marrow (BM) to peripheral blood (PB) involve modulation of adhesion molecule expression on these cells that probably result in changes in adhesion capacity to the microenvironment. However, it is not clear whether these changes involve different stages or lineages of progenitor cells. In this study, we compared the capacity of mature and immature clonogenic progenitor cells from granulocyte colony-stimulating factor (G-CSF)-mobilized PB and normal BM CD34+ cells to adhere to complete marrow stroma. This functional capacity was assessed concurrently with molecular expression on CD34+ cells of integrins VLA-4 (alpha 4/beta 1), VLA-5 (alpha 5/beta 1), and LFA-1 (alpha L/beta 2) by interindividual (between mobilized PB and normal BM) and intraindividual (between mobilized PB and steady-state BM and PB in the same patient) analysis. The proportion of adherent clonogenic progenitor cells was significantly lower in PB than in BM, not only for total progenitor cells but also for mature and immature progenitor cells, and the difference was found for granulocytic and particularly for erythroid lineages. The lower adhesion capacity of PB CD34+ cells to stroma was associated with decreased expression (signal/noise MFI ratio) of integrin alpha 4, beta 1, alpha L, and beta 2 chains whereas that of alpha 5 chain did not differ from BM cells with the lowest expression level. Similar differences in integrin expression levels were also found between mobilized PB and steady-state BM CD34+ cells in the same patient except for the alpha L chain. Moreover, we demonstrated for the first time a strong positive correlation between mobilizing capacity and expression levels on mobilized CD34+ cells for the LFA-1 alpha L chain but not for VLA-4 or VLA-5. In conclusion, the decreased adhesion capacity of mobilized PB progenitor cells to stroma involves different maturation stages and different lineages. This is associated with down-regulation of integrins VLA-4 and LFA-1, but mobilizing capacity appears positively correlated with LFA-1 levels.
导致造血细胞从骨髓(BM)动员至外周血(PB)的分子机制,涉及这些细胞上黏附分子表达的调节,这可能导致其与微环境黏附能力的改变。然而,尚不清楚这些变化是否涉及祖细胞的不同阶段或谱系。在本研究中,我们比较了来自粒细胞集落刺激因子(G-CSF)动员的外周血和正常骨髓CD34+细胞的成熟和未成熟克隆形成祖细胞黏附完整骨髓基质的能力。通过个体间(动员的外周血与正常骨髓之间)和个体内(同一患者动员的外周血与稳态骨髓及外周血之间)分析,同时评估了CD34+细胞上整合素VLA-4(α4/β1)、VLA-5(α5/β1)和LFA-1(αL/β2)的分子表达情况。不仅对于总祖细胞,而且对于成熟和未成熟祖细胞,外周血中黏附的克隆形成祖细胞比例均显著低于骨髓,并且在粒细胞谱系尤其是红系谱系中发现了这种差异。外周血CD34+细胞与基质的黏附能力较低,与整合素α4、β1、αL和β2链的表达降低(信号/噪声平均荧光强度比值)相关,而α5链的表达与表达水平最低的骨髓细胞无差异。除αL链外,在同一患者的动员外周血和稳态骨髓CD34+细胞之间也发现了整合素表达水平的类似差异。此外,我们首次证明,动员能力与动员的CD34+细胞上LFA-1αL链的表达水平呈强正相关,而与VLA-4或VLA-5无关。总之,动员的外周血祖细胞与基质的黏附能力降低涉及不同的成熟阶段和不同的谱系。这与整合素VLA-4和LFA-1的下调相关,但动员能力似乎与LFA-1水平呈正相关。