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本文引用的文献

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A network of transcription factors operates during early tooth morphogenesis.在早期牙齿形态发生过程中,转录因子网络发挥作用。
Mol Cell Biol. 2013 Aug;33(16):3099-112. doi: 10.1128/MCB.00524-13. Epub 2013 Jun 10.
2
Roles of Bmp4 during tooth morphogenesis and sequential tooth formation.Bmp4 在牙齿形态发生和连续牙齿形成中的作用。
Development. 2013 Jan 15;140(2):423-32. doi: 10.1242/dev.081927.
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A Wnt-bmp feedback circuit controls intertissue signaling dynamics in tooth organogenesis.Wnt-bmp 反馈回路控制牙齿器官发生中的组织间信号动态。
Sci Signal. 2012 Jan 10;5(206):ra4. doi: 10.1126/scisignal.2002414.
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Developmental stalling and organ-autonomous regulation of morphogenesis.发育停滞与器官自主调节形态发生。
Proc Natl Acad Sci U S A. 2011 Nov 29;108(48):19270-5. doi: 10.1073/pnas.1112801108. Epub 2011 Nov 14.
5
Osr2 acts downstream of Pax9 and interacts with both Msx1 and Pax9 to pattern the tooth developmental field.Osr2 在 Pax9 下游发挥作用,并与 Msx1 和 Pax9 相互作用,从而对牙齿发育区域进行模式化。
Dev Biol. 2011 May 15;353(2):344-53. doi: 10.1016/j.ydbio.2011.03.012. Epub 2011 Mar 17.
6
The T-box transcription factor Tbx2: its role in development and possible implication in cancer.T 盒转录因子 Tbx2:在发育中的作用及其在癌症中的可能意义。
IUBMB Life. 2010 Feb;62(2):92-102. doi: 10.1002/iub.275.
7
Molecular genetics of tooth development.牙齿发育的分子遗传学。
Curr Opin Genet Dev. 2009 Oct;19(5):504-10. doi: 10.1016/j.gde.2009.09.002. Epub 2009 Oct 28.
8
Expression and requirement of T-box transcription factors Tbx2 and Tbx3 during secondary palate development in the mouse.小鼠继发腭发育过程中T盒转录因子Tbx2和Tbx3的表达及需求
Dev Biol. 2009 Dec 15;336(2):145-55. doi: 10.1016/j.ydbio.2009.09.020. Epub 2009 Sep 19.
9
Enamel-free teeth: Tbx1 deletion affects amelogenesis in rodent incisors.无釉质牙齿:Tbx1基因缺失影响啮齿动物门齿的釉质形成。
Dev Biol. 2009 Apr 15;328(2):493-505. doi: 10.1016/j.ydbio.2009.02.014. Epub 2009 Feb 20.
10
Msx1 and Msx2 are functional interacting partners of T-box factors in the regulation of Connexin43.Msx1和Msx2是T-box因子在调控连接蛋白43过程中的功能性相互作用伙伴。
Cardiovasc Res. 2008 Jun 1;78(3):485-93. doi: 10.1093/cvr/cvn049. Epub 2008 Feb 19.

Msx1 和 Tbx2 在牙齿发育的芽-帽阶段过渡期间拮抗调节 Bmp4 的表达。

Msx1 and Tbx2 antagonistically regulate Bmp4 expression during the bud-to-cap stage transition in tooth development.

机构信息

Center for Regenerative and Developmental Biology, The Forsyth Institute, Cambridge, MA 02142, USA.

出版信息

Development. 2013 Jul;140(13):2697-702. doi: 10.1242/dev.088393. Epub 2013 May 29.

DOI:10.1242/dev.088393
PMID:23720046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3678339/
Abstract

Bmp4 expression is tightly regulated during embryonic tooth development, with early expression in the dental epithelial placode leading to later expression in the dental mesenchyme. Msx1 is among several transcription factors that are induced by epithelial Bmp4 and that, in turn, are necessary for the induction and maintenance of dental mesenchymal Bmp4 expression. Thus, Msx1(-/-) teeth arrest at early bud stage and show loss of Bmp4 expression in the mesenchyme. Ectopic expression of Bmp4 rescues this bud stage arrest. We have identified Tbx2 expression in the dental mesenchyme at bud stage and show that this can be induced by epithelial Bmp4. We also show that endogenous Tbx2 and Msx1 can physically interact in mouse C3H10T1/2 cells. In order to ascertain a functional relationship between Msx1 and Tbx2 in tooth development, we crossed Tbx2 and Msx1 mutant mice. Our data show that the bud stage tooth arrest in Msx1(-/-) mice is partially rescued in Msx1(-/-);Tbx2(+/-) compound mutants. This rescue is accompanied by formation of the enamel knot (EK) and by restoration of mesenchymal Bmp4 expression. Finally, knockdown of Tbx2 in C3H10T1/2 cells results in an increase in Bmp4 expression. Together, these data identify a novel role for Tbx2 in tooth development and suggest that, following their induction by epithelial Bmp4, Msx1 and Tbx2 in turn antagonistically regulate odontogenic activity that leads to EK formation and to mesenchymal Bmp4 expression at the key bud-to-cap stage transition.

摘要

Bmp4 的表达在胚胎牙齿发育过程中受到严格调控,早期在牙上皮嵴中的表达导致后期在牙间质中的表达。Msx1 是几个转录因子之一,这些转录因子被上皮 Bmp4 诱导,反过来又对牙间质 Bmp4 的诱导和维持是必需的。因此,Msx1(-/-)牙齿在早期芽期停滞,并且在间质中显示出 Bmp4 表达的丧失。Bmp4 的异位表达可挽救这种芽期阻滞。我们在芽期发现 Tbx2 在牙间质中的表达,并表明上皮 Bmp4 可以诱导其表达。我们还表明,内源性 Tbx2 和 Msx1 可以在小鼠 C3H10T1/2 细胞中物理相互作用。为了确定 Msx1 和 Tbx2 在牙齿发育中的功能关系,我们对 Tbx2 和 Msx1 突变小鼠进行了杂交。我们的数据表明,Msx1(-/-)小鼠的芽期牙齿阻滞在 Msx1(-/-);Tbx2(+/-)复合突变体中部分得到挽救。这种挽救伴随着牙结的形成和间质 Bmp4 表达的恢复。最后,在 C3H10T1/2 细胞中敲低 Tbx2 导致 Bmp4 表达增加。总之,这些数据确定了 Tbx2 在牙齿发育中的新作用,并表明,在它们被上皮 Bmp4 诱导后,Msx1 和 Tbx2 依次拮抗调节牙原性活性,导致 EK 形成和间质 Bmp4 表达在芽期到帽期的关键过渡。