Center for Regenerative and Developmental Biology, The Forsyth Institute, Cambridge, MA 02142, USA.
Development. 2013 Jul;140(13):2697-702. doi: 10.1242/dev.088393. Epub 2013 May 29.
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.
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。