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哺乳动物牙齿初始形态发生过程中上皮-间充质相互作用的分析。

Analysis of epithelial-mesenchymal interactions in the initial morphogenesis of the mammalian tooth.

作者信息

Dassule H R, McMahon A P

机构信息

The Biolabs, Harvard University, 16 Divinity Avenue, Cambridge, Massachusetts 02138, USA.

出版信息

Dev Biol. 1998 Oct 15;202(2):215-27. doi: 10.1006/dbio.1998.8992.

Abstract

Epithelial-mesenchymal interactions govern the development of epidermal organs such as teeth. During the early stages of tooth development, a local ectodermal thickening which expresses several signaling molecules appears. It is believed that these in turn signal to the underlying mesenchyme triggering mesenchymal condensation and tooth development. For example, epithelially expressed Bmp4 induces Msx1 and Lef1 as well as itself in the underlying mesenchyme. In this paper we have investigated the role of four epithelial signaling molecules, Bmp2, Shh, Wnt10a, and Wnt10b, in the early inductive cascades that govern tooth development. We show that all four genes are specifically expressed in the epithelium between E11.0 and E12.0 when tooth morphogenesis is first apparent. Although Shh, Bmp2, and Wnt10b have similar, if not identical, expression patterns, each signal has a distinct molecular action on the jaw mesenchyme. Whereas Shh and Wnt10b can induce general Hedgehog and Wnt targets, Ptc and Gli for Shh and Lef1 for Wnt10b, only Bmp2 is able to induce tooth-specific expression of Msx1. Thus, there are distinct targets for all three pathways. Interestingly, both Bmp and Wnt signaling activate Lef1, making it a candidate for integrating the two distinct signaling pathways.

摘要

上皮-间充质相互作用调控着牙齿等表皮器官的发育。在牙齿发育的早期阶段,会出现一个表达多种信号分子的局部外胚层增厚区。据信,这些信号分子会依次向下方的间充质发出信号,触发间充质凝聚和牙齿发育。例如,上皮表达的Bmp4会在下方间充质中诱导Msx1、Lef1以及其自身的表达。在本文中,我们研究了四种上皮信号分子Bmp2、Shh、Wnt10a和Wnt10b在调控牙齿发育的早期诱导级联反应中的作用。我们发现,在E11.0至E12.0期间,当牙齿形态发生首次明显出现时,所有这四个基因都在上皮中特异性表达。尽管Shh、Bmp2和Wnt10b具有相似(即便不是完全相同)的表达模式,但每个信号对颌间充质都有独特的分子作用。Shh和Wnt10b能够诱导一般的Hedgehog和Wnt靶基因,Shh诱导Ptc和Gli,Wnt10b诱导Lef1,而只有Bmp2能够诱导Msx1的牙齿特异性表达。因此,这三条信号通路都有各自不同的靶基因。有趣的是,Bmp和Wnt信号通路都能激活Lef1,这使得它成为整合这两条不同信号通路的一个候选分子。

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