Miyamoto A, Kunisada T, Hemmi H, Yamane T, Yasuda H, Miyake K, Yamazaki H, Hayashi S I
Department of Immunology, School of Life Science, Faculty of Medicine, Tottori University, Japan.
Biochem Biophys Res Commun. 1998 Jan 26;242(3):703-9. doi: 10.1006/bbrc.1997.8046.
Osteoclasts are hematopoietic cells essential for bone remodeling and resorption. To understand the process of osteoclast development, we established a macrophage-like cell line C7 that has the potential to differentiate into functional osteoclasts; multinuclear tartrate-resistant acid phosphatase positive cells capable of forming pits on dentin slices. C7 cells share the characteristics of their cell surface molecules and phagocytic activity with macrophages. Generation of osteoclasts from C7 cells was mostly suppressed by the addition of a function-blocking antibody directed to c-Fms, the receptor for macrophage-colony stimulating factor (M-CSF), or by osteoclastogenesis inhibitory factor (OCIF). These responses correspond well with the osteoclast precursors present in bone marrow and peritoneal cavity. Reagents such as bacterial lipopolysaccharide and granulocyte/macrophage-CSF that are known to act as inducers for other cell lineages rather than osteoclasts abolished the potential of osteoclastogenesis in C7 cells. These phenotypes of C7 cells have been stably maintained for more than 2 years. We believe that the cell line established in this study will provide an important tool for osteoclast biology.
破骨细胞是骨重塑和吸收所必需的造血细胞。为了解破骨细胞的发育过程,我们建立了一种巨噬细胞样细胞系C7,它具有分化为功能性破骨细胞的潜力;这种多核抗酒石酸酸性磷酸酶阳性细胞能够在牙本质切片上形成凹陷。C7细胞与巨噬细胞在细胞表面分子和吞噬活性方面具有共同特征。从C7细胞生成破骨细胞的过程大多受到针对c-Fms(巨噬细胞集落刺激因子(M-CSF)的受体)的功能阻断抗体或破骨细胞生成抑制因子(OCIF)的抑制。这些反应与存在于骨髓和腹腔中的破骨细胞前体情况高度相符。已知作为其他细胞谱系而非破骨细胞诱导剂的试剂,如细菌脂多糖和粒细胞/巨噬细胞集落刺激因子,消除了C7细胞的破骨细胞生成潜力。C7细胞的这些表型已稳定维持了两年多。我们相信本研究中建立的细胞系将为破骨细胞生物学提供一个重要工具。