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牙发生过程中的多效蛋白表达。

Pleiotrophin expression during odontogenesis.

机构信息

Institute of Oral Health Research, School of Dentistry, University of Alabama at Birmingham, Birmingham, Alabama 35294-0007, USA.

出版信息

J Histochem Cytochem. 2012 May;60(5):366-75. doi: 10.1369/0022155412439316. Epub 2012 Feb 29.

Abstract

Pleiotrophin (PTN) is an extracellular matrix-associated growth factor and chemokine expressed in mesodermal and ectodermal cells. It plays an important role in osteoblast recruitment and differentiation. There is limited information currently available about PTN expression during odontoblast differentiation and tooth formation, and thus the authors aimed to establish the spatiotemporal expression pattern of PTN during mouse odontogenesis. Immortalized mouse dental pulp (MD10-D3, MD10-A11) and odontoblast-like (M06-G3) and ameloblast-like (EOE-3M) cell lines were grown and samples prepared for immunocytochemistry, Western blot, and conventional and quantitative PCR analysis. Effects of BMP2, BMP4, and BMP7 treatment on PTN expression in odontoblast-like M06-G3 cells were tested by quantitative PCR. Finally, immunohistochemistry of sectioned mice mandibles and maxillaries at developmental stages E16, E18, P1, P6, P10, and P28 was performed. The experiments showed that PTN, at both the mRNA and protein level, was expressed in all tested epithelial and mesenchymal dental cell lines and that the level of PTN mRNA was influenced differentially by the bone morphogenetic proteins. The authors observed initial expression of PTN in the inner enamel epithelium with prolonged expression in the ameloblasts and odontoblasts throughout their stages of maturation and strong expression in the terminally differentiated and enamel matrix-secreting ameloblasts and odontoblasts of the adult mouse incisors and molars.

摘要

多效蛋白(PTN)是一种细胞外基质相关的生长因子和趋化因子,在中胚层和外胚层细胞中表达。它在成骨细胞的募集和分化中发挥重要作用。目前关于牙胚分化和牙齿形成过程中 PTN 的表达信息有限,因此作者旨在建立 PTN 在小鼠牙发生过程中的时空表达模式。永生的小鼠牙髓(MD10-D3、MD10-A11)和成牙本质细胞样(M06-G3)和成釉细胞样(EOE-3M)细胞系进行培养,并准备用于免疫细胞化学、Western blot 和常规及定量 PCR 分析的样本。通过定量 PCR 测试 BMP2、BMP4 和 BMP7 处理对成牙本质细胞样 M06-G3 细胞中 PTN 表达的影响。最后,对发育阶段 E16、E18、P1、P6、P10 和 P28 的小鼠下颌骨和上颌骨进行了免疫组织化学分析。实验表明,PTN 在所有测试的上皮和间充质牙细胞系中均在 mRNA 和蛋白质水平上表达,并且骨形态发生蛋白对 PTN mRNA 的水平有不同的影响。作者观察到 PTN 最初在釉内层上皮中表达,在成釉细胞和成牙本质细胞中持续表达,在成熟阶段和在终末分化的、分泌釉质基质的成釉细胞和成牙本质细胞中表达强烈,在成年小鼠切牙和磨牙中。

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