Clouthier David E, Gray Josie, Artinger Kristin Bruk
Department of Craniofacial Biology, University of Colorado Denver, Aurora, CO 80045, USA.
Perspect Speech Sci Orofac Disord. 2008 Oct 1;18(2):62-72. doi: 10.1044/ssod18.2.62.
Development of the facial skeleton is one of the most intriguing and intricate events that occur during human development. Most of the bone, cartilage and connective tissue that compose the face and neck arise from a class of cells, referred to as neural crest cells, which are initially located at some distance from the facial primordium. A complex set of events regulated by specific gene products direct the formation, migration and differentiation of these cells, leading to what is viewed as "prototypical" adult facial features. These basic developmental processes are recapitulated during the formation of the palate, termed palatogenesis. In this review, we summarize the basic embryology leading to palate formation, discuss mechanisms that can lead to palatal dysmorphologies and highlight a new interaction that has recently been demonstrated to play a role in palate development. This interaction, involving small non-coding RNAs referred to as microRNAs, not only establishes a new level of regulation to cellular development, but may also serve as attractive targets for future efforts directed at clinical treatment of birth defect syndromes.
面部骨骼的发育是人类发育过程中最引人入胜且错综复杂的事件之一。构成面部和颈部的大部分骨骼、软骨及结缔组织均起源于一类被称为神经嵴细胞的细胞,这些细胞最初位于距面部原基有一定距离之处。由特定基因产物调控的一系列复杂事件指导着这些细胞的形成、迁移和分化,最终形成被视为“典型”的成人面部特征。在腭部形成过程中,即腭发生过程中,会重现这些基本的发育过程。在本综述中,我们总结了导致腭形成的基本胚胎学知识,讨论了可能导致腭部畸形的机制,并着重介绍了最近被证明在腭部发育中起作用的一种新的相互作用。这种相互作用涉及被称为微小RNA的小非编码RNA,它不仅为细胞发育建立了一个新的调控层面,而且可能成为未来针对出生缺陷综合征进行临床治疗的有吸引力的靶点。