Sakiyama H, Masuda R, Inoue N, Yamamoto K, Kuriiwa K, Nakagawa K, Yoshida K
Division of Biology and Oncology, National Institute of Radiological Sciences, Chiba, Japan.
J Bone Miner Metab. 2001;19(4):220-7. doi: 10.1007/s007740170024.
Osteoclasts differentiate from hematopoietic precursors of the monocyte/macrophage lineage to mononuclear preosteoclasts and multinuclear mature osteoclasts. In the present study, we report on the establishment of macrophage like cell lines from mouse bone marrow by coculturing bone marrow cells with mouse chondrocytes. Isolated clones (MLC-6 and MLC-7 cells) expressed fully differentiated osteoclast markers, such as calcitonin receptors, vitronectin receptors, tartrate-resistant acid phosphatase and vacuolar H+ -ATPase, in the absence of osteoclast differentiation factor/osteoprotegerin ligand/RANKL/TRANCE, which was essential for osteoclast differentiation. Most clones also maintained expression of a macrophage-associated protein, namely non-specific esterase. Both MLC-6 and MLC-7 cells released cathepsin K into the culture medium. Both clones resolved dentine slices when cocultured with the osteoblast cell line ST2. The cloned cell lines are considered to be useful tools in the study of osteoclast differentiation.
破骨细胞从单核细胞/巨噬细胞谱系的造血前体分化为单核前破骨细胞和多核成熟破骨细胞。在本研究中,我们报告了通过将骨髓细胞与小鼠软骨细胞共培养,从小鼠骨髓建立巨噬细胞样细胞系。分离的克隆(MLC - 6和MLC - 7细胞)在缺乏破骨细胞分化因子/骨保护素配体/RANKL/TRANCE的情况下表达完全分化的破骨细胞标志物,如降钙素受体、玻连蛋白受体、抗酒石酸酸性磷酸酶和液泡H⁺ - ATP酶,而破骨细胞分化因子对破骨细胞分化至关重要。大多数克隆还维持巨噬细胞相关蛋白即非特异性酯酶的表达。MLC - 6和MLC - 7细胞均将组织蛋白酶K释放到培养基中。当与成骨细胞系ST2共培养时,两个克隆都能溶解牙本质切片。这些克隆细胞系被认为是研究破骨细胞分化的有用工具。