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大鼠钙化组织中44-kDa骨磷蛋白(骨桥蛋白)和骨γ-羧基谷氨酸(Gla)结合蛋白(骨钙素)的发育表达。

Developmental expression of 44-kDa bone phosphoprotein (osteopontin) and bone gamma-carboxyglutamic acid (Gla)-containing protein (osteocalcin) in calcifying tissues of rat.

作者信息

Mark M P, Butler W T, Prince C W, Finkelman R D, Ruch J V

机构信息

Institut de Biologie Medicale, Universite Louis Pasteur, Faculte de Medecine, Strasbourg, France.

出版信息

Differentiation. 1988;37(2):123-36. doi: 10.1111/j.1432-0436.1988.tb00804.x.

Abstract

New aspects of the distribution and developmental appearance of the 44-kDa bone phosphoprotein (44K BPP, also called sialoprotein I or osteopontin) and bone gamma-carboxyglutamic acid (Gla)-containing protein (BGP, also called osteocalcin) during osteogenesis and dentinogenesis were investigated with immunocytochemical techniques using monospecific, affinity-purified polyclonal antibodies. Sections from newborn rat incisors and from various bone anlagen of newborn animals and fetuses were processed for detection of 44K BPP or BGP antigenicity. In addition, histochemical reactions for detection of alkaline phosphatase or calcium salts were performed on a number of the sections. The 44K BPP appears to be synthesized and secreted by chondrocytes only in the areas of cartilage-to-bone transition; these cells could participate indirectly in the process of bone formation by providing a suitable scaffold onto which primary marrow osteoblasts attach and spread. During osteogenesis, 44K BPP is found in bone-forming cells almost concomitantly with the appearance of alkaline phosphatase and before osteoid deposition, whereas BGP is still absent during early stages of mineralization. We hypothesize that this dramatic difference between the developmental appearance of 44K BPP and BGP reflects the delayed expression of the BGP gene relative to that of 44K BPP. In long-term cultures of bone marrow from adult mice, some fibroblastic cells expressed the 44K BPP phenotype; these cells could represent early osteogenic progenitor cells. Some experiments also suggested that, as with BGP, 44K BPP or an immunologically related protein is synthesized by some odontoblasts and secreted into predentin, prior to the onset of mineralization.

摘要

利用单特异性、亲和纯化的多克隆抗体,采用免疫细胞化学技术,研究了44kDa骨磷蛋白(44K BPP,也称为涎蛋白I或骨桥蛋白)和骨γ-羧基谷氨酸(Gla)结合蛋白(BGP,也称为骨钙素)在骨生成和牙本质生成过程中的分布及发育表现的新方面。对新生大鼠切牙以及新生动物和胎儿的各种骨原基切片进行处理,以检测44K BPP或BGP抗原性。此外,对一些切片进行了检测碱性磷酸酶或钙盐的组织化学反应。44K BPP似乎仅由软骨向骨转变区域的软骨细胞合成和分泌;这些细胞可通过提供一个合适的支架,使初级骨髓成骨细胞附着并铺展,从而间接参与骨形成过程。在骨生成过程中,44K BPP在成骨细胞中出现的时间几乎与碱性磷酸酶同时,且早于类骨质沉积,而在矿化早期BGP仍然不存在。我们推测,44K BPP和BGP发育表现的这种显著差异反映了BGP基因相对于44K BPP基因的表达延迟。在成年小鼠骨髓的长期培养中,一些成纤维细胞表达了44K BPP表型;这些细胞可能代表早期成骨祖细胞。一些实验还表明,与BGP一样,44K BPP或一种免疫相关蛋白在矿化开始前由一些成牙本质细胞合成并分泌到前期牙本质中。

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