Gritli-Linde Amel
Department of Oral Biochemistry, Sahlgrenska Academy at Göteborg University, Medicinaregatan 12F, Göteborg, Sweden.
Dev Biol. 2007 Jan 15;301(2):309-26. doi: 10.1016/j.ydbio.2006.07.042. Epub 2006 Aug 5.
Compared with the embryonic development of other organs, development of the secondary palate is seemingly simple. However, each step of palatogenesis, from initiation until completion, is subject to a tight molecular control that is governed by epithelial-mesenchymal interactions. The importance of a rigorous molecular regulation of palatogenesis is reflected when loss of function of a single protein generates cleft palate, a frequent malformation with a complex etiology. Genetic studies in humans and targeted mutations in mice have identified numerous factors that play key roles during palatogenesis. This review highlights the current understanding of the molecular and cellular mechanisms involved in normal and abnormal palate development with special respect to recent advances derived from studies of mouse models.
与其他器官的胚胎发育相比,次生腭的发育看似简单。然而,从起始到完成的腭发生的每一步都受到上皮-间充质相互作用所支配的严格分子控制。当单一蛋白质的功能丧失导致腭裂(一种病因复杂的常见畸形)时,就体现了腭发生严格分子调控的重要性。人类的遗传学研究和小鼠的靶向突变已经确定了许多在腭发生过程中起关键作用的因素。本综述着重介绍了目前对正常和异常腭发育所涉及的分子和细胞机制的理解,特别关注了来自小鼠模型研究的最新进展。