Denkers I A, de Jong-de Boer T J, Beelen R H, Ossenkoppele G J, Nauta J J, Langenhuijsen M M
Department of Haematology, Free University, Amsterdam, The Netherlands.
Leuk Res. 1993 Mar;17(3):255-61. doi: 10.1016/0145-2126(93)90009-a.
In order to study the adhesive interactions of the human bone marrow microenvironment and acute myeloid leukaemic cells, we investigated the binding capacity of KG-1 cells upon human long-term bone marrow cultures derived from 17 healthy volunteers and 12 patients with acute myeloid leukemia. Adhesion was measured using a 51-chromium labelling assay. Adhesion of KG-1 cells upon 'normal' stromal layers: 33% +/- 4.0, n = 17 (mean +/- SEM) was higher as compared to the binding to 'leukaemic' stromas: 24% +/- 3.7, n = 12 (p < 0.05). Blocking monoclonal antibodies against adhesion molecules reduced the binding of KG-1 cells upon 'normal' stroma, when anti-VLA4 (p < 0.03), anti-Mac1 (p < 0.03) and anti-p150/95 (p < 0.04) were used. Binding of KG-1 cells on 'leukaemic' stromas was partly inhibited by anti-VCAM1 (p < 0.03). Blocking achieved by single or combined antibodies was never complete, suggesting that the adhesion is a multifactorial process, including a variety of adhesion molecules and/or adhesion mechanisms.
为了研究人类骨髓微环境与急性髓系白血病细胞的黏附相互作用,我们调查了KG-1细胞对来自17名健康志愿者和12名急性髓系白血病患者的人类长期骨髓培养物的黏附能力。使用51铬标记试验测量黏附情况。与黏附于“白血病”基质相比,KG-1细胞黏附于“正常”基质层的情况:33%±4.0,n = 17(平均值±标准误)更高,黏附于“白血病”基质的情况为:24%±3.7,n = 12(p < 0.05)。当使用抗VLA4(p < 0.03)、抗Mac1(p < 0.03)和抗p150/95(p < 0.04)时,针对黏附分子的阻断单克隆抗体降低了KG-1细胞在“正常”基质上的黏附。抗VCAM1(p < 0.03)部分抑制了KG-1细胞在“白血病”基质上的黏附。单一抗体或联合抗体实现的阻断从未完全,这表明黏附是一个多因素过程,包括多种黏附分子和/或黏附机制。