Jimi E, Akiyama S, Tsurukai T, Okahashi N, Kobayashi K, Udagawa N, Nishihara T, Takahashi N, Suda T
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan.
J Immunol. 1999 Jul 1;163(1):434-42.
Osteoclast differentiation factor (ODF), a novel member of the TNF ligand family, is expressed as a membrane-associated protein by osteoblasts/stromal cells. The soluble form of ODF (sODF) induces the differentiation of osteoclast precursors into osteoclasts in the presence of M-CSF. Here, the effects of sODF on the survival, multinucleation, and pit-forming activity of murine osteoclasts were examined in comparison with those of M-CSF and IL-1. Osteoclast-like cells (OCLs) formed in cocultures of murine osteoblasts and bone marrow cells expressed mRNA of RANK (receptor activator of NF-kappaB), a receptor of ODF. The survival of OCLs was enhanced by the addition of each of sODF, M-CSF, and IL-1. sODF, as well as IL-1, activated NF-kappaB and c-Jun N-terminal protein kinase (JNK) in OCLs. Like M-CSF and IL-1, sODF stimulated the survival and multinucleation of prefusion osteoclasts (pOCs) isolated from the coculture. When pOCs were cultured on dentine slices, resorption pits were formed on the slices in the presence of either sODF or IL-1 but not in that of M-CSF. A soluble form of RANK as well as osteoprotegerin/osteoclastogenesis inhibitory factor, a decoy receptor of ODF, blocked OCL formation and prevented the survival, multinucleation, and pit-forming activity of pOCs induced by sODF. These results suggest that ODF regulates not only osteoclast differentiation but also osteoclast function in mice through the receptor RANK.
破骨细胞分化因子(ODF)是肿瘤坏死因子配体家族的一个新成员,由成骨细胞/基质细胞作为膜相关蛋白表达。ODF的可溶性形式(sODF)在M-CSF存在的情况下可诱导破骨细胞前体分化为破骨细胞。在此,将sODF与M-CSF和IL-1相比,研究了其对小鼠破骨细胞存活、多核化及陷窝形成活性的影响。在小鼠成骨细胞与骨髓细胞共培养物中形成的破骨细胞样细胞(OCLs)表达ODF受体RANK(核因子κB受体激活剂)的mRNA。添加sODF、M-CSF和IL-1中的任何一种均可增强OCLs的存活。sODF以及IL-1可激活OCLs中的核因子κB和c-Jun氨基末端蛋白激酶(JNK)。与M-CSF和IL-1一样,sODF可刺激从共培养物中分离出的融合前破骨细胞(pOCs)的存活和多核化。当将pOCs培养在牙本质切片上时,在sODF或IL-1存在的情况下,切片上会形成吸收陷窝,而在M-CSF存在的情况下则不会。可溶性形式的RANK以及ODF的诱饵受体骨保护素/破骨细胞生成抑制因子可阻断OCL形成,并阻止sODF诱导的pOCs的存活、多核化及陷窝形成活性。这些结果表明,ODF在小鼠中不仅通过RANK受体调节破骨细胞分化,还调节破骨细胞功能。