Zhang Zunyi, Song Yiqiang, Zhang Xiaoyun, Tang Jean, Chen Jinkun, Chen YiPing
Department of Cell and Molecular Biology, Tulane University, 2000 Stern Hall, 6400 Freret St, New Orleans, LA 70118, USA. zzhang
Mech Dev. 2003 Dec;120(12):1469-79. doi: 10.1016/j.mod.2003.09.002.
In the developing mammalian tooth, the cranial neural crest derived dental mesenchyme consists of the dental papilla and dental follicle. The dental papilla gives rise to odontoblasts and dental pulp and the dental follicle gives rise to the periodontium, including the osteoblasts that contribute to the alveolar process. The alveolar process is a specialized intramembranous bone that forms the primary support structure for the dentition. The Msx1 gene controls many aspects of craniofacial development, as evidenced by craniofacial abnormalities seen in Msx1(-/-) mice, including the arrest of tooth development and the absence of the alveolar bone. Previous studies demonstrated that ectopic expression of Bmp4, a downstream target of Msx1, in the Msx1(-/-) dental mesenchyme rescued alveolar bone formation. Here we confirm an early requirement of BMP activity for alveolar bone formation. We show that the expression of Cbfa1 and Dlx5, two genes encode transcription factors that are critical for bone differentiation, overlaps with that of Msx1 and Bmp4 in the developing tooth and alveolar process. We have demonstrated that Dlx5 and Cbfa1 expression is down-regulated in Msx1(-/-) dental mesenchyme and that Msx1 and Bmp4 expression are unaltered in Cbfa1(-/-) mice. These data place Dlx5 and Cbfa1 downstream from the Msx1/Bmp4 in the genetic pathway that regulates tooth development. Ectopic expression of Bmp4 in Msx1 mutants restores the expression of Dlx5, but not Cbfa1, in the dental mesenchyme, and rescues the expression of both Dlx5 and Cbfa1 in the developing alveolar bone. Therefore, the early expression of Cfba1 in the dental mesenchyme appears dispensable for the development of the alveolar bone. Taken together with in vitro gene induction studies, our results demonstrate that BMP4 controls Dlx5 expression in dental mesenchyme, and functions upstream to both Dlx5 and Cbfa1 to regulate alveolar bone formation during tooth development.
在发育中的哺乳动物牙齿中,源自颅神经嵴的牙间充质由牙乳头和牙囊组成。牙乳头产生成牙本质细胞和牙髓,牙囊产生牙周组织,包括对牙槽突有贡献的成骨细胞。牙槽突是一种特殊的膜内骨,形成牙列的主要支撑结构。Msx1基因控制颅面发育的许多方面,Msx1(-/-)小鼠出现的颅面异常证明了这一点,包括牙齿发育停滞和牙槽骨缺失。先前的研究表明,Msx1的下游靶点Bmp4在Msx1(-/-)牙间充质中的异位表达挽救了牙槽骨的形成。在这里,我们证实了BMP活性对牙槽骨形成的早期需求。我们表明,Cbfa1和Dlx5这两个编码对骨分化至关重要的转录因子的基因的表达,与Msx1和Bmp4在发育中的牙齿和牙槽突中的表达重叠。我们已经证明,Dlx5和Cbfa1的表达在Msx1(-/-)牙间充质中下调,而Msx1和Bmp4的表达在Cbfa1(-/-)小鼠中未改变。这些数据表明,在调节牙齿发育的遗传途径中,Dlx5和Cbfa1位于Msx1/Bmp4的下游。Bmp4在Msx1突变体中的异位表达恢复了牙间充质中Dlx5的表达,但没有恢复Cbfa1的表达,并挽救了发育中的牙槽骨中Dlx5和Cbfa1的表达。因此,Cbfa1在牙间充质中的早期表达似乎对牙槽骨的发育是可有可无的。结合体外基因诱导研究,我们的结果表明,BMP4控制牙间充质中Dlx5的表达,并在Dlx5和Cbfa1的上游发挥作用,以调节牙齿发育过程中的牙槽骨形成。