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早期牙齿发育过程中细胞与组织相互作用的分子机制

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

作者信息

Thesleff I, Vaahtokari A, Vainio S, Jowett A

机构信息

Institute of Dentistry, University of Helsinki, Finland.

出版信息

Anat Rec. 1996 Jun;245(2):151-61. doi: 10.1002/(SICI)1097-0185(199606)245:2<151::AID-AR4>3.0.CO;2-#.

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.

摘要

背景

包括牙齿在内的所有器官在发育过程中的形态发生和细胞分化是由细胞与组织之间的相互作用所调控的。正在发育的牙齿是此类相互作用的分子机制开始得以阐明的器官之一。

结果

同型细胞相互作用发生在具有相同发育历程的细胞之间,并且它们是牙齿发育芽期期间间充质细胞凝聚物形成的核心机制。Syndecan-1,一种细胞表面硫酸乙酰肝素蛋白聚糖,在牙间充质中短暂表达,并可能调节牙间充质细胞凝聚。它结合腱生蛋白,一种在牙间充质中丰富的基质糖蛋白,提示细胞 - 基质相互作用的参与。Syndecan还结合生长因子,并且它与牙间充质中细胞增殖的关联提示其在调控凝聚细胞中细胞数量方面的作用。上皮组织和间充质组织之间的诱导性相互作用在牙齿发育的所有阶段均调控牙齿发育。在早期牙间充质中,包括syndecan和腱生蛋白在内的几种分子的表达受上皮组织调控。有证据表明生长因子作为可扩散信号介导这些相互作用。属于TGFβ超家族的骨形态发生蛋白BMP-2和BMP-4在早期牙上皮中表达,并且它们对牙间充质的作用模拟上皮组织的作用。特别地,BMPs诱导牙间充质中含同源框转录因子Msx-1和Msx-2的表达。

结论

基于目前关于伴随牙齿发育的分子变化的知识以及实验研究结果,我们提出了一个早期牙齿发育分子调控的模型。

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