The heterogeneity of the osteopetroses reflects the diversity of cellular influences during skeletal development
Identifieur interne : 00A591 ( Main/Curation ); précédent : 00A590; suivant : 00A592The heterogeneity of the osteopetroses reflects the diversity of cellular influences during skeletal development
Auteurs : S. N. Popoff [États-Unis] ; S. C. Marks Jr. [États-Unis]Source :
- Bone [ 8756-3282 ] ; 1995.
Descripteurs français
- Wicri :
- topic : Mineur (ouvrier).
English descriptors
- KwdEn :
- Abnormality, Acad, Additional studies, Binding protein, Biochem, Biol, Bone cells, Bone miner, Bone resorption, Carbonic anhydrase, Cecchini, Cell biochem, Cell biol, Cell biology, Cellular, Cellular diversity, Cellular diversity bone, Clin, Clinical applications, Congenital osteopetrosis, Cytokine, Defect, Diverse effects, Free radicals, Gene, Gene expression, Growth factor, Growth factors, Hemopoietic, Hemopoietic growth factors, High levels, Immune, Immune cells, Immune regulators, Immune system, Interferon, Kinase, Lineage, Lymphocyte, Macrophage, Macrophage activation, Macrophage development, Macrophage factor, Malignant osteopetrosis, Mammalian osteopetroses, Mature osteoclasts, Miner, Mouse, Mundy, Mutant, Mutation, Natl, Normal littermates, November, Oncogene, Osteoblast, Osteoblast differentiation, Osteoclast, Osteoclast development, Osteoclast function, Osteoclastic bone resorption, Osteopetroses, Osteopetrosis, Osteopetrotic, Osteopetrotic animals, Osteopetrotic children, Osteopetrotic mouse, Osteopetrotic mutations, Osteopetrotic rats, Osteosarcoma, Parathyroid hormone, Phagocyte, Popoff, Potent macrophage, Proc, Proc natl acad, Recent studies, Receptor, Resorption, Schneider, Sclerosis, Skeletal development, Skeletal effects, Skeletal sclerosis, Spleen cells, Superoxide, Transgenic mice, Transplantation, Tyrosine kinases.
- Teeft :
- Abnormality, Acad, Additional studies, Binding protein, Biochem, Biol, Bone cells, Bone miner, Bone resorption, Carbonic anhydrase, Cecchini, Cell biochem, Cell biol, Cell biology, Cellular, Cellular diversity, Cellular diversity bone, Clin, Clinical applications, Congenital osteopetrosis, Cytokine, Defect, Diverse effects, Free radicals, Gene, Gene expression, Growth factor, Growth factors, Hemopoietic, Hemopoietic growth factors, High levels, Immune, Immune cells, Immune regulators, Immune system, Interferon, Kinase, Lineage, Lymphocyte, Macrophage, Macrophage activation, Macrophage development, Macrophage factor, Malignant osteopetrosis, Mammalian osteopetroses, Mature osteoclasts, Miner, Mouse, Mundy, Mutant, Mutation, Natl, Normal littermates, November, Oncogene, Osteoblast, Osteoblast differentiation, Osteoclast, Osteoclast development, Osteoclast function, Osteoclastic bone resorption, Osteopetroses, Osteopetrosis, Osteopetrotic, Osteopetrotic animals, Osteopetrotic children, Osteopetrotic mouse, Osteopetrotic mutations, Osteopetrotic rats, Osteosarcoma, Parathyroid hormone, Phagocyte, Popoff, Potent macrophage, Proc, Proc natl acad, Recent studies, Receptor, Resorption, Schneider, Sclerosis, Skeletal development, Skeletal effects, Skeletal sclerosis, Spleen cells, Superoxide, Transgenic mice, Transplantation, Tyrosine kinases.
Abstract
Abstract: Experimental studies of the mammalian osteopetroses, characterized by generalized skeletal sclerosis, have illuminated a variety of mechanisms by which bone resorption can be reduced. We review recent data implicating a diverse group of growth factors, proto-oncogenes, and immune regulators that can influence skeletal development and account for the heterogeneity of the osteopetroses. Furthermore, similar studies are likely to continue to provide for improved clinical management of both osteopetrotic children and the localized and generalized osteopenias.
Url:
DOI: 10.1016/8756-3282(95)00347-4
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ISTEX:7A65D753CF4E33032C2203B2318C95161F8BCF67Le document en format XML
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<term>Biol</term>
<term>Bone cells</term>
<term>Bone miner</term>
<term>Bone resorption</term>
<term>Carbonic anhydrase</term>
<term>Cecchini</term>
<term>Cell biochem</term>
<term>Cell biol</term>
<term>Cell biology</term>
<term>Cellular</term>
<term>Cellular diversity</term>
<term>Cellular diversity bone</term>
<term>Clin</term>
<term>Clinical applications</term>
<term>Congenital osteopetrosis</term>
<term>Cytokine</term>
<term>Defect</term>
<term>Diverse effects</term>
<term>Free radicals</term>
<term>Gene</term>
<term>Gene expression</term>
<term>Growth factor</term>
<term>Growth factors</term>
<term>Hemopoietic</term>
<term>Hemopoietic growth factors</term>
<term>High levels</term>
<term>Immune</term>
<term>Immune cells</term>
<term>Immune regulators</term>
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<term>Kinase</term>
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<term>Macrophage activation</term>
<term>Macrophage development</term>
<term>Macrophage factor</term>
<term>Malignant osteopetrosis</term>
<term>Mammalian osteopetroses</term>
<term>Mature osteoclasts</term>
<term>Miner</term>
<term>Mouse</term>
<term>Mundy</term>
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<term>Mutation</term>
<term>Natl</term>
<term>Normal littermates</term>
<term>November</term>
<term>Oncogene</term>
<term>Osteoblast</term>
<term>Osteoblast differentiation</term>
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<term>Osteopetrotic children</term>
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<term>Osteopetrotic mutations</term>
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<term>Proc natl acad</term>
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<term>Resorption</term>
<term>Schneider</term>
<term>Sclerosis</term>
<term>Skeletal development</term>
<term>Skeletal effects</term>
<term>Skeletal sclerosis</term>
<term>Spleen cells</term>
<term>Superoxide</term>
<term>Transgenic mice</term>
<term>Transplantation</term>
<term>Tyrosine kinases</term>
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<term>Acad</term>
<term>Additional studies</term>
<term>Binding protein</term>
<term>Biochem</term>
<term>Biol</term>
<term>Bone cells</term>
<term>Bone miner</term>
<term>Bone resorption</term>
<term>Carbonic anhydrase</term>
<term>Cecchini</term>
<term>Cell biochem</term>
<term>Cell biol</term>
<term>Cell biology</term>
<term>Cellular</term>
<term>Cellular diversity</term>
<term>Cellular diversity bone</term>
<term>Clin</term>
<term>Clinical applications</term>
<term>Congenital osteopetrosis</term>
<term>Cytokine</term>
<term>Defect</term>
<term>Diverse effects</term>
<term>Free radicals</term>
<term>Gene</term>
<term>Gene expression</term>
<term>Growth factor</term>
<term>Growth factors</term>
<term>Hemopoietic</term>
<term>Hemopoietic growth factors</term>
<term>High levels</term>
<term>Immune</term>
<term>Immune cells</term>
<term>Immune regulators</term>
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<term>Interferon</term>
<term>Kinase</term>
<term>Lineage</term>
<term>Lymphocyte</term>
<term>Macrophage</term>
<term>Macrophage activation</term>
<term>Macrophage development</term>
<term>Macrophage factor</term>
<term>Malignant osteopetrosis</term>
<term>Mammalian osteopetroses</term>
<term>Mature osteoclasts</term>
<term>Miner</term>
<term>Mouse</term>
<term>Mundy</term>
<term>Mutant</term>
<term>Mutation</term>
<term>Natl</term>
<term>Normal littermates</term>
<term>November</term>
<term>Oncogene</term>
<term>Osteoblast</term>
<term>Osteoblast differentiation</term>
<term>Osteoclast</term>
<term>Osteoclast development</term>
<term>Osteoclast function</term>
<term>Osteoclastic bone resorption</term>
<term>Osteopetroses</term>
<term>Osteopetrosis</term>
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<term>Osteopetrotic children</term>
<term>Osteopetrotic mouse</term>
<term>Osteopetrotic mutations</term>
<term>Osteopetrotic rats</term>
<term>Osteosarcoma</term>
<term>Parathyroid hormone</term>
<term>Phagocyte</term>
<term>Popoff</term>
<term>Potent macrophage</term>
<term>Proc</term>
<term>Proc natl acad</term>
<term>Recent studies</term>
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<term>Resorption</term>
<term>Schneider</term>
<term>Sclerosis</term>
<term>Skeletal development</term>
<term>Skeletal effects</term>
<term>Skeletal sclerosis</term>
<term>Spleen cells</term>
<term>Superoxide</term>
<term>Transgenic mice</term>
<term>Transplantation</term>
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<front><div type="abstract" xml:lang="en">Abstract: Experimental studies of the mammalian osteopetroses, characterized by generalized skeletal sclerosis, have illuminated a variety of mechanisms by which bone resorption can be reduced. We review recent data implicating a diverse group of growth factors, proto-oncogenes, and immune regulators that can influence skeletal development and account for the heterogeneity of the osteopetroses. Furthermore, similar studies are likely to continue to provide for improved clinical management of both osteopetrotic children and the localized and generalized osteopenias.</div>
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