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两种与矿物质相关的黏附分子骨桥蛋白和骨唾液蛋白在牙骨质形成过程中的作用。

Role of two mineral-associated adhesion molecules, osteopontin and bone sialoprotein, during cementogenesis.

作者信息

MacNeil R L, Berry J, D'Errico J, Strayhorn C, Piotrowski B, Somerman M J

机构信息

Department of Periodontics/Prevention and Geriatrics, School of Dentistry, University of Michigan, Ann Arbor 48109-1078, USA.

出版信息

Connect Tissue Res. 1995;33(1-3):1-7. doi: 10.3109/03008209509016974.

DOI:10.3109/03008209509016974
PMID:7554941
Abstract

Adhesion molecules and their cell membrane receptors are known to play important regulatory roles in cell differentiation. Consequently, the following experiments were conducted to determine the role of two adhesion molecules, bone sialoprotein (BSP) and osteopontin (OPN) in tooth root formation. Developing murine molar tooth germs at sequential stages of development (developmental days 21-42) were analyzed using immunohistochemical and in situ hybridization techniques. While BSP was localized to alveolar bone and odontoblasts early in development, BSP was distinctly localized to the cemental root surface at latter periods coincident with the initiation of root formation and cementogenesis. Conversely, OPN was distributed in a nonspecific fashion throughout the PDL and the eruption pathway of the forming tooth. In situ hybridization confirmed that cells lining the root surface express BSP. The fact that BSP is specifically localized to the cemental surface suggests that this protein is involved in cementoblast differentiation and/or early mineralization of the cementum matrix. Localization of OPN to non-mineralized tissues further suggests that OPN functions as an inhibitor of mineralization during periodontal ligament formation. These findings collectively suggest that BSP and OPN are intimately involved in the sequence of cellular and molecular events accompanying cementogenesis.

摘要

已知黏附分子及其细胞膜受体在细胞分化中发挥重要的调节作用。因此,进行了以下实验来确定两种黏附分子,即骨唾液蛋白(BSP)和骨桥蛋白(OPN)在牙根形成中的作用。使用免疫组织化学和原位杂交技术分析了发育阶段(发育天数21 - 42天)连续的小鼠磨牙牙胚。在发育早期,BSP定位于牙槽骨和成牙本质细胞,而在发育后期,与牙根形成和牙骨质生成开始同时,BSP明显定位于牙骨质根面。相反,OPN以非特异性方式分布于整个牙周膜和正在萌出牙齿的萌出道。原位杂交证实根面衬里细胞表达BSP。BSP特异性定位于牙骨质表面这一事实表明该蛋白参与成牙骨质细胞分化和/或牙骨质基质的早期矿化。OPN定位于非矿化组织进一步表明OPN在牙周膜形成过程中作为矿化抑制剂发挥作用。这些发现共同表明BSP和OPN密切参与伴随牙骨质生成的细胞和分子事件序列。

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