Hawley R G, Fong A Z, Ngan B Y, de Lanux V M, Clark S C, Hawley T S
Division of Cancer Research, Sunnybrook Health Science Centre, Toronto, Ontario, Canada.
J Exp Med. 1993 Oct 1;178(4):1175-88. doi: 10.1084/jem.178.4.1175.
Post 5-fluorouracil-treated murine bone marrow cells infected with a recombinant retrovirus (murine stem cell virus-interleukin 11 [MSCV-IL-11]) bearing a human IL-11 gene were transplanted into lethally irradiated syngeneic mice. Analysis of proviral integration sites in DNA prepared from hematopoietic tissues and purified cell populations of long-term reconstituted primary and secondary recipients demonstrated polyclonal engraftment by multipotential stem cells. High levels (100-1,500 U/ml) of IL-11 were detected in the plasma of the MSCV-IL-11 mice. Systemic effects of chronic IL-11 exposure included loss of body fat, thymus atrophy, some alterations in plasma protein levels, frequent inflammation of the eyelids, and often a hyperactive state. A sustained rise in peripheral platelet levels (approximately 1.5-fold) was seen throughout the observation period (4-17 wk). No changes were observed in the total number of circulating leukocytes in the majority of the transplanted animals (including 10 primary and 18 secondary recipients) despite a > 20-fold elevation in myeloid progenitor cell content in the spleen. The exceptions were members of one transplant pedigree which presented with myeloid leukemia during the secondary transplant phase. A clonal origin of the disease was determined, with significant expansion of the MSCV-IL-11-marked clone having occurred in the spleen of the primary host. Culturing of leukemic spleen cells from a quaternary recipient led to the establishment of a permanent cell line (denoted PGMD1). IL-11-producing PGMD1 myeloid leukemic cells are dependent on IL-3 for continuous growth in vitro and they differentiate into granulocytes and macrophages in response to granulocyte/macrophage colony-stimulating factor. The inability of autogenously produced IL-11 to support autonomous growth of PGMD1 cells argues against a mechanism of transformation involving a classical autocrine loop.
将携带人白细胞介素11(IL-11)基因的重组逆转录病毒(鼠干细胞病毒-白细胞介素11 [MSCV-IL-11])感染的经5-氟尿嘧啶处理的鼠骨髓细胞移植到接受致死剂量照射的同基因小鼠体内。对长期重建的原代和二代受体的造血组织及纯化细胞群体制备的DNA中的前病毒整合位点进行分析,结果表明多能干细胞实现了多克隆植入。在MSCV-IL-11小鼠的血浆中检测到高水平(100 - 1500 U/ml)的IL-11。长期暴露于IL-11的全身影响包括体脂减少、胸腺萎缩、血浆蛋白水平的一些改变、眼睑频繁发炎以及常出现多动状态。在整个观察期(4 - 17周)外周血小板水平持续升高(约1.5倍)。在大多数移植动物(包括10只原代受体和18只二代受体)中,尽管脾脏中髓系祖细胞含量升高超过20倍,但循环白细胞总数未观察到变化。唯一的例外是一个移植谱系中的成员,它们在二次移植阶段出现了髓系白血病。确定了该疾病的克隆起源,在原代宿主的脾脏中MSCV-IL-11标记的克隆发生了显著扩增。从四代受体的白血病脾脏细胞培养建立了一个永久细胞系(命名为PGMD1)。产生IL-11的PGMD1髓系白血病细胞在体外持续生长依赖于IL-3,并且它们在粒细胞/巨噬细胞集落刺激因子的作用下分化为粒细胞和巨噬细胞。内源性产生的IL-11无法支持PGMD1细胞的自主生长,这与涉及经典自分泌环的转化机制相悖。