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      Bone resorption by osteoclasts.

      Science (New York, N.Y.)
      Animals, Bone Resorption, Carrier Proteins, metabolism, Cell Differentiation, Cell Membrane, physiology, ultrastructure, Glycoproteins, Humans, Integrins, Macrophage Colony-Stimulating Factor, Macrophages, cytology, Membrane Glycoproteins, Osteoclasts, Osteopetrosis, genetics, Osteoprotegerin, RANK Ligand, Receptor Activator of Nuclear Factor-kappa B, Receptors, Cytoplasmic and Nuclear, Receptors, Tumor Necrosis Factor, Stromal Cells

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          Abstract

          Osteoporosis, a disease endemic in Western society, typically reflects an imbalance in skeletal turnover so that bone resorption exceeds bone formation. Bone resorption is the unique function of the osteoclast, and anti-osteoporosis therapy to date has targeted this cell. The osteoclast is a specialized macrophage polykaryon whose differentiation is principally regulated by macrophage colony-stimulating factor, RANK ligand, and osteoprotegerin. Reflecting integrin-mediated signals, the osteoclast develops a specialized cytoskeleton that permits it to establish an isolated microenvironment between itself and bone, wherein matrix degradation occurs by a process involving proton transport. Osteopetrotic mutants have provided a wealth of information about the genes that regulate the differentiation of osteoclasts and their capacity to resorb bone.

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