Filshie R, Gottlieb D, Bradstock K
Department of Haematology, Westmead Hospital, New South Wales, Australia.
Br J Haematol. 1998 Sep;102(5):1292-300. doi: 10.1046/j.1365-2141.1998.00899.x.
Attachment of human pre-B leukaemic cells to human or murine bone marrow stromal cells in vitro is largely mediated by the beta1 integrin VLA-4 binding to VCAM-1. Cells subsequently migrate within the stroma, a process also involving VLA-4. A variant of the pre-B acute lymphoblastic leukaemia cell line NALM-6, designated 4A1, lacking expression of VLA-4, was generated by radiation-induced mutagenesis followed by several rounds of negative selection with immunomagnetic beads, fluorescence activated cell sorting and clonal expansion. In vitro assays using 4A1 cells showed reduced binding to, and migration under, the murine stromal line M2-10B4. Sublethally irradiated mice (n=19) with severe combined immunodeficiency were injected intravenously with NALM-6 cells. Animals developed signs of leukaemia with hind-limb paralysis at a median of 30 d (95% confidence interval 28-30). Although there were no gross abnormal findings at autopsy, histological analysis revealed extensive marrow replacement and focal liver infiltration with leukaemic blasts, which were confirmed to be of human origin by flow cytometry. 12 mice were injected with a similar number of cells from the VLA-4-negative variant cell line 4A1. Six mice developed signs of leukaemia after 43-74d, with the remaining six being free of signs of disease after > 100d (P<0.001). Mice in this group with leukaemia had a lower incidence of hind-limb paralysis and less leukaemic infiltration in the marrow, but in some cases had large tumour nodules elsewhere. After a single 500 microg intraperitoneal injection of anti-murine VCAM-1 monoclonal antibody (MK2.7), five additional mice were injected with an identical number of wild-type (VLA-4+) NALM-6. All animals developed signs of leukaemia after a similar period to those injected with wild-type NALM-6 only. These results demonstrate that the beta1 integrin VLA-4 is involved in the engraftment of the pre-B-cell leukaemic cell line NALM-6 in SCID mice, although the interaction with VCAM-1 is unlikely to be the sole explanation.
人前B淋巴细胞白血病细胞在体外与人或鼠骨髓基质细胞的黏附,很大程度上是由β1整合素VLA-4与血管细胞黏附分子-1(VCAM-1)结合介导的。随后细胞在基质内迁移,这一过程也涉及VLA-4。通过辐射诱变,然后用免疫磁珠进行多轮阴性选择、荧光激活细胞分选和克隆扩增,产生了前B急性淋巴细胞白血病细胞系NALM-6的一个变体,命名为4A1,其缺乏VLA-4的表达。使用4A1细胞进行的体外试验显示,其与鼠基质细胞系M2-10B4的黏附及在其下的迁移减少。对19只患有严重联合免疫缺陷的亚致死剂量照射小鼠静脉注射NALM-6细胞。动物在中位30天(95%置信区间28 - 30)出现白血病体征并伴有后肢麻痹。尽管尸检时没有明显异常发现,但组织学分析显示有广泛的骨髓被白血病母细胞替代以及局灶性肝浸润,通过流式细胞术证实这些白血病母细胞来源于人。给12只小鼠注射了相似数量的来自VLA-4阴性变体细胞系4A1的细胞。6只小鼠在43 - 74天后出现白血病体征,其余6只在超过100天后无疾病体征(P<0.001)。该组患有白血病的小鼠后肢麻痹发生率较低,骨髓中的白血病浸润较少,但在某些情况下其他部位有大的肿瘤结节。在单次腹腔注射500微克抗鼠VCAM-1单克隆抗体(MK2.7)后,给另外5只小鼠注射相同数量的野生型(VLA-4+)NALM-6。所有动物在与仅注射野生型NALM-6的动物相似的时间段后出现白血病体征。这些结果表明,β1整合素VLA-4参与了前B细胞白血病细胞系NALM-6在SCID小鼠中的植入,尽管与VCAM-1的相互作用不太可能是唯一的解释。