Hofstetter W, Wetterwald A, Cecchini M C, Felix R, Fleisch H, Mueller C
Department of Pathophysiology, University of Berne, Switzerland.
Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9637-41. doi: 10.1073/pnas.89.20.9637.
Macrophage colony-stimulating factor (M-CSF), whose action is restricted to the cell populations of the mononuclear phagocyte system, has recently been found to be required for osteoclastogenesis and bone resorption. To investigate the cells involved in the action of M-CSF in these processes, expression of c-fms mRNA, encoding the M-CSF receptor, was studied by in situ hybridization. Paws from murine embryos and newborn mice, tibiae from 2-day-old animals, as well as isolated osteoclasts, were hybridized with a c-fms-specific RNA probe. In bone, c-fms mRNA was detected only in cells at the late stages of osteoclastogenesis and in mature osteoclasts. The findings strengthen the relation between osteoclasts and the mononuclear phagocyte system. Furthermore, they suggest that M-CSF acts directly on osteoclast precursors and on mature osteoclasts during osteoclastogenesis.
巨噬细胞集落刺激因子(M-CSF)的作用仅限于单核吞噬细胞系统的细胞群体,最近发现它是破骨细胞生成和骨吸收所必需的。为了研究参与M-CSF在这些过程中作用的细胞,通过原位杂交研究了编码M-CSF受体的c-fms mRNA的表达。将来自小鼠胚胎和新生小鼠的爪子、2日龄动物的胫骨以及分离的破骨细胞与c-fms特异性RNA探针杂交。在骨中,仅在破骨细胞生成后期的细胞和成熟破骨细胞中检测到c-fms mRNA。这些发现加强了破骨细胞与单核吞噬细胞系统之间的关系。此外,它们表明M-CSF在破骨细胞生成过程中直接作用于破骨细胞前体和成熟破骨细胞。