Hattersley G, Owens J, Flanagan A M, Chambers T J
Dept. of Histopathology, St George's Hospital Medical School, London, UK.
Biochem Biophys Res Commun. 1991 May 31;177(1):526-31. doi: 10.1016/0006-291x(91)92015-c.
The op/op mouse, in which the M-CSF gene is mutated, has greatly reduced numbers of macrophages and osteoclasts. We assessed the ability of M-CSF to induce osteoclast and macrophage formation in op/op hemopoietic cells in vitro. Osteoclast production was undetectable in op/op cell cultures, but was restored by M-CSF at concentrations approximately an order of magnitude higher than those that induced macrophages. In normal hemopoietic tissue M-CSF similarly increased macrophage numbers, but inhibited osteoclast formation. Despite cure of the macrophage defect, neither interleukin 3 nor granulocyte-macrophage CSF were able to induce osteoclastic differentiation in op/op cells. The results suggest that M-CSF induces osteoclastic differentiation but that macrophages, which are also induced by M-CSF, suppress osteoclast differentiation. Macrophages induced by other cytokines seem unable to contribute to osteoclast-formation.
op/op小鼠的M-CSF基因发生突变,其巨噬细胞和破骨细胞数量大幅减少。我们评估了M-CSF在体外诱导op/op造血细胞形成破骨细胞和巨噬细胞的能力。在op/op细胞培养物中未检测到破骨细胞生成,但M-CSF以比诱导巨噬细胞的浓度高约一个数量级的浓度可使其恢复。在正常造血组织中,M-CSF同样增加了巨噬细胞数量,但抑制了破骨细胞形成。尽管巨噬细胞缺陷得到治愈,但白细胞介素3和粒细胞-巨噬细胞集落刺激因子均不能诱导op/op细胞发生破骨细胞分化。结果表明,M-CSF诱导破骨细胞分化,但由M-CSF诱导的巨噬细胞会抑制破骨细胞分化。其他细胞因子诱导的巨噬细胞似乎无法促进破骨细胞形成。