
Osteoclasts are bone-resorbing multinucleated cells derived from the monocyte-macrophage lineage. The authors have developed a mouse marrow culture system and a coculture system of mouse osteoblasts and hemopoietic cells, in which osteoclasts are formed in response to various osteotropic factors such as 1alpha,25-dihydroxyvitamin D3, parathyroid hormone, prostaglandin E2, and interleukin-11. Recent studies have revealed that osteoblasts express two cytokines essential for osteoclastogenesis: receptor activator of nuclear factor kappaB ligand (RANKL) and macrophage colony-stimulating factor (M-CSF). Using RANKL and M-CSF, we can induce osteoclasts from monocyte-macrophage lineage cells even in the absence of osteoblasts. This chapter describes the methods for osteoclast formation in vitro in the presence and absence of osteoblasts, and for pit-formation assay using dentine slices and osteoclasts formed in vitro. These culture systems have made it possible to investigate each step of osteoclast development and function separately.
Osteoblasts, Macrophage Colony-Stimulating Factor, Macrophages, Cathepsin K, Bone Marrow Cells, Cell Differentiation, Cell Separation, Buffers, Cathepsins, Immunohistochemistry, Models, Biological, Actins, Coculture Techniques, Cell Line, Culture Media, Mice, Animals, Collagen, Bone Resorption, Gels
Osteoblasts, Macrophage Colony-Stimulating Factor, Macrophages, Cathepsin K, Bone Marrow Cells, Cell Differentiation, Cell Separation, Buffers, Cathepsins, Immunohistochemistry, Models, Biological, Actins, Coculture Techniques, Cell Line, Culture Media, Mice, Animals, Collagen, Bone Resorption, Gels
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