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釉结作为连接牙齿形态发生和成牙本质细胞分化的信号中心。

Enamel knots as signaling centers linking tooth morphogenesis and odontoblast differentiation.

作者信息

Thesleff I, Keränen S, Jernvall J

机构信息

Developmental Biology Program, Institute of Biotechnology, Vlikki Biocenter, 00014 University of Helsinki, Finland.

出版信息

Adv Dent Res. 2001 Aug;15:14-8. doi: 10.1177/08959374010150010401.

Abstract

Odontoblasts differentiate from the cells of the dental papilla, and it has been well-established that their differentiation in developing teeth is induced by the dental epithelium. In experimental studies, no other mesenchymal cells have been shown to have the capacity to differentiate into odontoblasts, indicating that the dental papilla cells have been committed to odontoblast cell lineage during earlier developmental stages. We propose that the advancing differentiation within the odontoblast cell lineage is regulated by sequential epithelial signals. The first epithelial signals from the early oral ectoderm induce the odontogenic potential in the cranial neural crest cells. The next step in the determination of the odontogenic cell lineage is the development of the dental papilla from odontogenic mesenchyme. The formation of the dental papilla starts at the onset of the transition from the bud to the cap stage of tooth morphogenesis, and this is regulated by epithelial signals from the primary enamel knot. The primary enamel knot is a signaling center which forms at the tip of the epithelial tooth bud. It becomes fully developed and morphologically discernible in the cap-stage dental epithelium and expresses at least ten different signaling molecules belonging to the BMP, FGF, Hh, and Wnt families. In molar teeth, secondary enamel knots appear in the enamel epithelium at the sites of the future cusps. They also express several signaling molecules, and their formation precedes the folding and growth of the epithelium. The differentiation of odontoblasts always starts from the tips of the cusps, and therefore, it is conceivable that some of the signals expressed in the enamel knots may act as inducers of odontoblast differentiation. The functions of the different signals in enamel knots are not precisely known. We have shown that FGFs stimulate the proliferation of mesenchymal as well as epithelial cells, and they may also regulate the growth of the cusps. We have proposed that the enamel knot signals also have important roles, together with mesenchymal signals, in regulating the patterning of the cusps and hence the shape of the tooth crown. We suggest that the enamel knots are central regulators of tooth development, since they link cell differentiation to morphogenesis.

摘要

成牙本质细胞由牙乳头细胞分化而来,并且已经明确的是,它们在发育中的牙齿中的分化是由牙上皮诱导的。在实验研究中,没有其他间充质细胞被证明有能力分化为成牙本质细胞,这表明牙乳头细胞在早期发育阶段就已确定为成牙本质细胞谱系。我们提出,成牙本质细胞谱系内的进一步分化是由一系列上皮信号调节的。来自早期口腔外胚层的第一批上皮信号诱导颅神经嵴细胞中的牙源性潜能。确定牙源性细胞谱系的下一步是由牙源性间充质发育出牙乳头。牙乳头的形成始于牙齿形态发生从芽期向帽状期转变之时,这是由来自初级釉结的上皮信号调节的。初级釉结是一个信号中心,形成于上皮牙芽的顶端。它在帽状期牙上皮中充分发育并在形态上可辨认,并且表达至少十种属于BMP、FGF、Hh和Wnt家族的不同信号分子。在磨牙中,次级釉结出现在未来牙尖部位的釉上皮中。它们也表达几种信号分子,并且它们的形成先于上皮的折叠和生长。成牙本质细胞的分化总是从牙尖开始,因此,可以想象釉结中表达的一些信号可能作为成牙本质细胞分化的诱导剂。釉结中不同信号的功能尚不完全清楚。我们已经表明,FGFs刺激间充质细胞和上皮细胞的增殖,并且它们也可能调节牙尖的生长。我们提出,釉结信号与间充质信号一起,在调节牙尖的形态以及因此牙冠的形状方面也具有重要作用。我们认为釉结是牙齿发育的核心调节因子,因为它们将细胞分化与形态发生联系起来。

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