Metcalf D, Nicola N A, Gough N M, Elliott M, McArthur G, Li M
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.
Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2819-23. doi: 10.1073/pnas.89.7.2819.
Cells of the continuous murine hemopoietic cell line FDC-P1 expressing macrophage-colony-stimulating factor (M-CSF) receptors following retroviral insertion of murine c-fms cDNA proliferated clonally when stimulated by granulocyte/macrophage (GM)-CSF, multipotential CSF, or M-CSF. However, M-CSF combined with either GM-CSF or multi-CSF, even at low CSF concentrations, strongly inhibited colony formation, with loss of clonogenicity in affected cells accompanied by increased macrophage differentiation. Stimulation by these CSF combinations did not induce short-term changes in CSF receptor expression or internalization. FDC-P1 cells expressing another inserted tyrosine kinase receptor, basic fibroblast growth factor receptor, did not exhibit suppression when GM-CSF was combined with fibroblast growth factor. This phenomenon of synergistic suppression may have relevance for the future clinical use of combinations of CSFs, because a potentially similar suppression is also observable with some normal macrophage progenitor cells.
在逆转录病毒插入小鼠c-fms cDNA后表达巨噬细胞集落刺激因子(M-CSF)受体的连续小鼠造血细胞系FDC-P1细胞,在受到粒细胞/巨噬细胞(GM)-CSF、多能CSF或M-CSF刺激时会进行克隆增殖。然而,M-CSF与GM-CSF或多能CSF联合使用时,即使在低CSF浓度下,也会强烈抑制集落形成,受影响细胞的克隆形成能力丧失,同时巨噬细胞分化增加。这些CSF组合的刺激并未诱导CSF受体表达或内化的短期变化。表达另一种插入的酪氨酸激酶受体(碱性成纤维细胞生长因子受体)的FDC-P1细胞,在GM-CSF与成纤维细胞生长因子联合使用时未表现出抑制作用。这种协同抑制现象可能与CSF组合在未来临床应用中的相关性有关,因为在一些正常巨噬细胞祖细胞中也可观察到潜在的类似抑制作用。