Yao G-Q, Sun B H, Weir E C, Insogna K L
Section of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Calcif Tissue Int. 2002 Apr;70(4):339-46. doi: 10.1007/s00223-001-1079-x. Epub 2002 Apr 3.
CSF-1 is required for osteoblast-mediated osteoclast formation. Osteoblasts produce soluble (sCSF-1) and cell-surface forms of CSF-1 (also known as membrane-bound CSF-1, mCSF-1) but their individual contributions to osteoclastogenesis remain unclear. Using glutaraldehyde-fixed primary murine osteoblasts as a source of mCSF-1, osteoblasts from op/op mice as a source for other osteoblast-derived osteoclastogenic factors and murine bone marrow as a source of osteoclast progenitors, osteoclast-like cells (OCL) formation was observed after 7-9 days of co-culture. In contrast, no OCL formation occurred when mCSF-1 expressed by primary murine osteoblasts was blocked by CSF-1 antibody pretreatment or when op/op osteoblasts were substituted for primary murine osteoblasts in the co-culture system. Osteoclast formation was also significantly inhibited when murine primary osteoblasts were pretreated with an antisense phosphorothioate oligonucleotide against mCSF-1. Finally, mCSF-1 and sCSF-1 were synergistic in stimulating OCL formation. These data support the conclusion that mCSF-1 plays an important role in osteoblast-mediated osteoclastogenesis within the bone microenvironment.
成骨细胞介导破骨细胞形成需要集落刺激因子-1(CSF-1)。成骨细胞可产生可溶性CSF-1(sCSF-1)和细胞表面形式的CSF-1(也称为膜结合CSF-1,mCSF-1),但它们对破骨细胞生成的各自贡献仍不清楚。使用戊二醛固定的原代小鼠成骨细胞作为mCSF-1的来源,op/op小鼠的成骨细胞作为其他成骨细胞衍生的破骨细胞生成因子的来源,以及小鼠骨髓作为破骨细胞祖细胞的来源,共培养7-9天后观察到破骨细胞样细胞(OCL)形成。相反,当原代小鼠成骨细胞表达的mCSF-1被CSF-1抗体预处理阻断时,或在共培养系统中用op/op成骨细胞替代原代小鼠成骨细胞时,未发生OCL形成。当用针对mCSF-1的反义硫代磷酸酯寡核苷酸预处理小鼠原代成骨细胞时,破骨细胞形成也受到显著抑制。最后,mCSF-1和sCSF-1在刺激OCL形成方面具有协同作用。这些数据支持以下结论:mCSF-1在骨微环境中成骨细胞介导的破骨细胞生成中起重要作用。