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SIBLING蛋白在大鼠牙本质和骨的有机相和无机相中的分布。

Distribution of SIBLING proteins in the organic and inorganic phases of rat dentin and bone.

作者信息

Huang Bingzhen, Sun Yao, Maciejewska Izabela, Qin Disheng, Peng Tao, McIntyre Bradley, Wygant James, Butler William T, Qin Chunlin

机构信息

Department of Biomedical Sciences, Baylor College of Dentistry, Texas A & M University System Health Science Center, Dallas, TX 75246, USA.

出版信息

Eur J Oral Sci. 2008 Apr;116(2):104-12. doi: 10.1111/j.1600-0722.2008.00522.x.

Abstract

The SIBLING protein family is a group of non-collagenous proteins (NCPs) that includes dentin sialophosphoprotein (DSPP), dentin matrix protein 1 (DMP1), bone sialoprotein (BSP), and osteopontin (OPN). In the present study, we compared these four proteins in different phases of rat dentin and bone. First, we extracted NCPs in the unmineralized matrices and cellular compartments using guanidium-HCl (G1). Second, we extracted NCPs closely associated with hydroxyapatite using an EDTA solution (E). Last, we extracted the remaining NCPs again with guanidium-HCl (G2). Each fraction of Q-Sepharose ion-exchange chromatography was analyzed using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), Stains-All stain, and with western immunoblotting. In dentin, the NH(2)-terminal fragment of DSPP and its proteoglycan form were primarily present in the G1 extract, whereas the COOH-terminal fragment of DSPP was present exclusively in the E extract. The processed NH(2)-terminal fragment of DMP1 was present in G1 and E extracts, whereas the COOH-terminal fragment of DMP1 existed mainly in the E extract. Bone sialoprotein was present in all three extracts of dentin and bone, whereas OPN was present only in the G1 and E extracts of bone. The difference in the distribution of the SIBLING proteins between organic and inorganic phases supports the belief that these molecular species play different roles in dentinogenesis and osteogenesis.

摘要

SIBLING蛋白家族是一组非胶原蛋白(NCPs),包括牙本质涎磷蛋白(DSPP)、牙本质基质蛋白1(DMP1)、骨涎蛋白(BSP)和骨桥蛋白(OPN)。在本研究中,我们比较了这四种蛋白在大鼠牙本质和骨不同阶段的情况。首先,我们使用盐酸胍(G1)从未矿化基质和细胞区室中提取NCPs。其次,我们使用乙二胺四乙酸溶液(E)提取与羟基磷灰石紧密相关的NCPs。最后,我们再次用盐酸胍(G2)提取剩余的NCPs。使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)、全染染色和western免疫印迹分析Q-琼脂糖离子交换色谱的每个组分。在牙本质中,DSPP的NH(2)-末端片段及其蛋白聚糖形式主要存在于G1提取物中,而DSPP的COOH-末端片段仅存在于E提取物中。DMP1的加工后的NH(2)-末端片段存在于G1和E提取物中,而DMP1的COOH-末端片段主要存在于E提取物中。骨涎蛋白存在于牙本质和骨的所有三种提取物中,而OPN仅存在于骨的G1和E提取物中。SIBLING蛋白在有机相和无机相之间分布的差异支持了这些分子在牙本质形成和骨形成中发挥不同作用的观点。

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