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首页> 外文期刊>Development >Cbfa1 is required for epithelial-mesenchymal interactions regulating tooth development in mice.
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Cbfa1 is required for epithelial-mesenchymal interactions regulating tooth development in mice.

机译:Cbfa1是调节小鼠牙齿发育的上皮-间质相互作用所必需的。

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摘要

Osteoblasts and odontoblasts, cells that are responsible for the formation of bone and dentin matrices respectively, share several molecular characteristics. Recently, Cbfa1 was shown to be a critical transcriptional regulator of osteoblast differentiation. Mutations in this gene cause cleidocranial dysplasia (CCD), an autosomal dominant disorder in humans and mice characterized by defective bone formation. CCD also results in dental defects that include supernumerary teeth and delayed eruption of permanent dentition. The dental abnormalities in CCD suggest an important role for this molecule in the formation of dentition. Here we describe results of studies aimed at understanding the functions of Cbfa1 in tooth formation. RT-PCR and in situ hybridization analyses show that Cbfa1 has a unique expression pattern in dental mesenchyme from the bud to early bell stages during active epithelial morphogenesis. Unlike that observed in osteoblast differentiation, Cbfa1 is downregulated in fully differentiated odontoblasts and is surprisingly expressed in ectodermally derived ameloblasts during the maturation phase of enamel formation. The role of Cbfa1 in tooth morphogenesis is further illustrated by the misshapen and severely hypoplastic tooth organs in Cbfa1-/- mice. These tooth organs lacked overt odontoblast and ameloblast differentiation and normal dentin and enamel matrices. Epithelial-mesenchymal recombinants demonstrate that dental epithelium regulates mesenchymal Cbfa1 expression during the bud and cap stages and that these effects are mimicked by the FGFs but not by the BMPs as shown by our bead implantation assays. We propose that Cbfa1 regulates the expression of molecules in mesenchyme that act reciprocally on dental epithelium to control its growth and differentiation. Taken together, our data indicate a non-redundant role for Cbfa1 in tooth development that may be distinct from that in bone formation. In odontogenesis, Cbfa1 is not involved in the early signaling networks regulating tooth initiation and early morphogenesis but regulates key epithelial-mesenchymal interactions that control advancing morphogenesis and histodifferentiation of the epithelial enamel organ.
机译:成骨细胞和成牙本质细胞是分别负责骨骼和牙本质基质形成的细胞,具有一些分子特征。最近,Cbfa1被证明是成骨细胞分化的关键转录调节因子。该基因的突变会导致脑颅发育不良(CCD),这是人和小鼠的常染色体显性遗传疾病,特征是骨骼形成缺陷。 CCD还导致牙齿畸形,其中包括多余的牙齿和永久性齿列的延迟萌发。 CCD中的牙齿异常提示该分子在牙列形成中的重要作用。在这里,我们描述了旨在了解Cbfa1在牙齿形成中的功能的研究结果。 RT-PCR和原位杂交分析表明,Cbfa1在活跃的上皮形态发生过程中,从芽到钟形早期在牙间充质中具有独特的表达模式。与在成骨细胞分化中观察到的不同,Cbfa1在完全分化的成牙本质细胞中被下调,并且在釉质形成的成熟阶段令人惊讶地在外胚层衍生的成釉细胞中表达。 Cbfa1-/-小鼠的畸形和严重增生的牙齿器官进一步说明了Cbfa1在牙齿形态发生中的作用。这些牙齿器官缺乏明显的成牙本质细胞和成釉细胞分化能力以及正常的牙本质和牙釉质基质。上皮-间充质重组体表明,牙齿上皮在芽和帽阶段调节间充质Cbfa1表达,并且这些效应可以通过FGF模仿,而不能通过BMP模仿,如我们的珠子植入试验所示。我们建议,Cbfa1调节间质中分子的表达,这些分子相互作用于牙齿上皮以控制其生长和分化。综上所述,我们的数据表明Cbfa1在牙齿发育中的非冗余作用可能与骨骼形成中的作用不同。在牙本质发生中,Cbfa1不参与调节牙齿萌发和早期形态发生的早期信号网络,但调节着关键的上皮-间质相互作用,从而控制上皮釉质器官的形态发生和组织分化。

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