Brailly H, Pebusque M J, Tabilio A, Mannoni P
Immunotech S.A., Marseille, France.
Leukemia. 1993 Oct;7(10):1557-63.
Acute myeloid leukemia (AML) cells are dependent for their survival and proliferation on hematopoietic growth factors. As tumor necrosis factor alpha (TNF alpha) can increase the proliferation of primary cultures of AML cells, we have investigated the effect of TNF alpha on the autocrine and/or paracrine growth control by one of the major AML growth factor, granulocyte-macrophage colony-stimulating factor (GM-CSF). First, a panel of AML cells were analysed with respect to their proliferative response to TNF alpha. We provide experimental evidence that TNF alpha induces both GM-CSF gene expression and up-regulation of high-affinity GM-CSF membrane receptor in TNF alpha-responsive cells. This effect is not restricted to the malignant phenotype, although it could account for the selective growth advantage of the leukemic clone over the normal cells upon TNF alpha stimulation.
急性髓系白血病(AML)细胞的存活和增殖依赖于造血生长因子。由于肿瘤坏死因子α(TNFα)可增加AML细胞原代培养物的增殖,我们研究了TNFα对AML主要生长因子之一粒细胞-巨噬细胞集落刺激因子(GM-CSF)自分泌和/或旁分泌生长控制的影响。首先,分析了一组AML细胞对TNFα的增殖反应。我们提供的实验证据表明,TNFα可诱导TNFα反应性细胞中GM-CSF基因表达及高亲和力GM-CSF膜受体上调。这种效应并不局限于恶性表型,尽管它可能解释了TNFα刺激后白血病克隆相对于正常细胞的选择性生长优势。