Molecular mechanisms of cell and tissue interactions during early tooth development.

4区 医学 Q2 Agricultural and Biological Sciences Anatomical Record Pub Date : 1996-06-01 DOI:10.1002/(SICI)1097-0185(199606)245:2<151::AID-AR4>3.0.CO;2-#
I Thesleff, A Vaahtokari, S Vainio, A Jowett
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引用次数: 76

Abstract

Background: Morphogenesis and cell differentiation during the development of all organs, including the tooth, are regulated by interactions between cells and tissues. The developing tooth is one of the organs in which the molecular mechanisms of such interactions are starting to be elucidated.

Results: Homotypic cell interactions take place between cells of the same developmental history, and they are a central mechanism in the formation of mesenchymal cell condensates during the bud stage of tooth development. Syndecan-1, a cell surface heparan sulfate proteoglycan, is transiently expressed in the dental mesenchyme and may regulate dental mesenchymal cell condensation. It binds tenascin, a matrix glycoprotein abundant in dental mesenchyme, suggesting involvement of cell-matrix interactions. Syndecan also binds growth factors, and its association with cell proliferation in the dental mesenchyme suggests roles in the regulation of cell number in the condensing cells. Inductive interactions between the epithelial and mesenchymal tissues regulate tooth development at all stages. In the early dental mesenchyme, the expression of several molecules, including syndecan and tenascin, are regulated by the epithelium. There is evidence that growth factors act as diffusible signals mediating these interactions. BMP-2 and BMP-4 (bone morphogenetic proteins), which belong to the TGF beta superfamily, are expressed in the early dental epithelium, and their effects on the dental mesenchyme mimic those of the epithelium. In particular, BMPs induce the expression of the homeobox-containing transcription factors Msx-1 and Msx-2 in the dental mesenchyme.

Conclusions: Based on current knowledge about the molecular changes accompanying tooth development and the results of experimental studies, we present a model for molecular regulation of early tooth development.

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早期牙齿发育过程中细胞和组织相互作用的分子机制。
背景:在包括牙齿在内的所有器官的发育过程中,细胞的形成和分化都受到细胞和组织之间相互作用的调控。发育中的牙齿是这种相互作用的分子机制开始被阐明的器官之一。结果:同型细胞相互作用发生在具有相同发育历史的细胞之间,是牙发育芽期间充质细胞凝聚物形成的主要机制。Syndecan-1是一种细胞表面硫酸肝素蛋白多糖,在牙间质中短暂表达,可能调节牙间质细胞的凝聚。它与牙间质中丰富的基质糖蛋白tenascin结合,提示参与细胞-基质相互作用。Syndecan还结合生长因子,其与牙间质细胞增殖的关系提示其在凝聚细胞中起调节细胞数量的作用。上皮组织和间充质组织之间的诱导相互作用调节着牙齿发育的各个阶段。在早期牙间质中,syndecan和tenascin等分子的表达受上皮的调控。有证据表明,生长因子作为扩散信号介导这些相互作用。TGF β超家族的BMP-2和BMP-4(骨形态发生蛋白)在早期牙上皮中表达,其对牙间质的影响与上皮相似。特别是,bmp诱导含有同源盒的转录因子Msx-1和Msx-2在牙间质中的表达。结论:基于目前对牙齿发育过程中分子变化的认识和实验研究结果,我们提出了一个早期牙齿发育的分子调控模型。
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来源期刊
Anatomical Record
Anatomical Record Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
4.30
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0.00%
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期刊介绍: The Anatomical Record
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