{"title":"5骨形态发生蛋白","authors":"T. Katagiri, T. Suda, K. Miyazono","doi":"10.1101/087969752.50.121","DOIUrl":null,"url":null,"abstract":"Bone morphogenetic proteins (BMPs) have critical roles in skeletal development by regulating the proliferation, differentiation, and apoptosis of many types of cells. Molecular cloning of BMPs and identification of molecules homologous to them have shed light on the novel functions of BMPs in vertebrates as well as in invertebrates, including Drosophila and nematodes. In this chapter, we describe biochemical properties and biological activities of BMPs; we focus, in particular, on the cell differentiation induced by BMPs. Although BMPs are now known to be multifunctional factors in vertebrates and invertebrates, they were originally discovered and identified as a bone-inducing activity in bone matrix in 1965. Marshall R. Urist (1965) first prepared demineralized bone by treating bone with hydrochloric acid and then implanting the demineralized bone in muscular tissues. A few weeks after transplantation, he found that new cartilage and bone tissues with bone marrow had been ectopically formed in muscular tissue (Urist 1965). These findings clearly indicated that the demineralized bone matrix contained unknown bioactive substance(s) capable of inducing differentiation of bone-forming cells in muscular tissues. This ectopic bone-inducing activity was subsequently named “bone morphogenetic protein,” because it disappeared after trypsin digestion (Urist and Strates 1971). However, all attempts to isolate and identify BMP were unsuccessful for more than 20 years after Urist’s original findings because of the difficulty in isolating BMP from bone matrix. BMP activity was water insoluble and could be extracted from demineralized bone matrix with protein denaturants (Urist and Strates 1971; Sampath and Reddi 1981; Yoshikawa et...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"69 1","pages":"121-149"},"PeriodicalIF":0.0000,"publicationDate":"2008-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"43","resultStr":"{\"title\":\"5 The Bone Morphogenetic Proteins\",\"authors\":\"T. Katagiri, T. Suda, K. Miyazono\",\"doi\":\"10.1101/087969752.50.121\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Bone morphogenetic proteins (BMPs) have critical roles in skeletal development by regulating the proliferation, differentiation, and apoptosis of many types of cells. Molecular cloning of BMPs and identification of molecules homologous to them have shed light on the novel functions of BMPs in vertebrates as well as in invertebrates, including Drosophila and nematodes. In this chapter, we describe biochemical properties and biological activities of BMPs; we focus, in particular, on the cell differentiation induced by BMPs. Although BMPs are now known to be multifunctional factors in vertebrates and invertebrates, they were originally discovered and identified as a bone-inducing activity in bone matrix in 1965. Marshall R. Urist (1965) first prepared demineralized bone by treating bone with hydrochloric acid and then implanting the demineralized bone in muscular tissues. A few weeks after transplantation, he found that new cartilage and bone tissues with bone marrow had been ectopically formed in muscular tissue (Urist 1965). These findings clearly indicated that the demineralized bone matrix contained unknown bioactive substance(s) capable of inducing differentiation of bone-forming cells in muscular tissues. This ectopic bone-inducing activity was subsequently named “bone morphogenetic protein,” because it disappeared after trypsin digestion (Urist and Strates 1971). However, all attempts to isolate and identify BMP were unsuccessful for more than 20 years after Urist’s original findings because of the difficulty in isolating BMP from bone matrix. 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引用次数: 43
摘要
骨形态发生蛋白(BMPs)通过调节多种细胞的增殖、分化和凋亡,在骨骼发育中起着至关重要的作用。bmp的分子克隆和同源分子的鉴定揭示了bmp在脊椎动物和无脊椎动物(包括果蝇和线虫)中的新功能。在本章中,我们描述了bmp的生化特性和生物活性;我们特别关注bmp诱导的细胞分化。虽然bmp现在被认为是脊椎动物和无脊椎动物的多功能因子,但它们最初是在1965年发现并确定为骨基质中的骨诱导活性。Marshall R. Urist(1965)首先用盐酸处理骨,然后将脱矿骨植入肌肉组织,制备脱矿骨。移植几周后,他发现肌肉组织中异位形成了新的带有骨髓的软骨和骨组织(Urist 1965)。这些发现清楚地表明,脱矿骨基质中含有未知的生物活性物质,能够诱导肌肉组织中骨形成细胞的分化。这种异位骨诱导活性后来被命名为“骨形态发生蛋白”,因为它在胰蛋白酶消化后消失了(Urist和Strates, 1971)。然而,在Urist最初的发现之后的20多年里,所有分离和鉴定BMP的尝试都没有成功,因为从骨基质中分离BMP很困难。BMP的活性是不溶于水的,可以用蛋白质变性剂从脱矿骨基质中提取(Urist and Strates 1971;Sampath and Reddi 1981;Yoshikawa等……
Bone morphogenetic proteins (BMPs) have critical roles in skeletal development by regulating the proliferation, differentiation, and apoptosis of many types of cells. Molecular cloning of BMPs and identification of molecules homologous to them have shed light on the novel functions of BMPs in vertebrates as well as in invertebrates, including Drosophila and nematodes. In this chapter, we describe biochemical properties and biological activities of BMPs; we focus, in particular, on the cell differentiation induced by BMPs. Although BMPs are now known to be multifunctional factors in vertebrates and invertebrates, they were originally discovered and identified as a bone-inducing activity in bone matrix in 1965. Marshall R. Urist (1965) first prepared demineralized bone by treating bone with hydrochloric acid and then implanting the demineralized bone in muscular tissues. A few weeks after transplantation, he found that new cartilage and bone tissues with bone marrow had been ectopically formed in muscular tissue (Urist 1965). These findings clearly indicated that the demineralized bone matrix contained unknown bioactive substance(s) capable of inducing differentiation of bone-forming cells in muscular tissues. This ectopic bone-inducing activity was subsequently named “bone morphogenetic protein,” because it disappeared after trypsin digestion (Urist and Strates 1971). However, all attempts to isolate and identify BMP were unsuccessful for more than 20 years after Urist’s original findings because of the difficulty in isolating BMP from bone matrix. BMP activity was water insoluble and could be extracted from demineralized bone matrix with protein denaturants (Urist and Strates 1971; Sampath and Reddi 1981; Yoshikawa et...