Laboratory of Molecular Cell Biology, College of Pharmacy and Nutrition, University of Saskatchewan Saskatoon, SK, Canada.
Front Physiol. 2013 Jan 7;3:488. doi: 10.3389/fphys.2012.00488. eCollection 2012.
Cleft palate is a common congenital birth defect in humans. In mammals, the palatal tissue can be distinguished into anterior bony hard palate and posterior muscular soft palate that have specialized functions in occlusion, speech or swallowing. Regulation of palate development appears to be the result of distinct signaling and genetic networks in the anterior and posterior regions of the palate. Development and maintenance of expression of these region-specific genes is crucial for normal palate development. Numerous transcription factors and signaling pathways are now recognized as either anterior- (e.g., Msx1, Bmp4, Bmp2, Shh, Spry2, Fgf10, Fgf7, and Shox2) or posterior-specific (e.g., Meox2, Tbx22, and Barx1). Localized expression and function clearly highlight the importance of regional patterning and differentiation within the palate at the molecular level. Here, we review how these molecular pathways and networks regulate the anterior-posterior patterning and development of secondary palate. We hypothesize that the anterior palate acts as a signaling center in setting up development of the secondary palate.
腭裂是人类常见的先天性出生缺陷。在哺乳动物中,腭组织可分为前部骨性硬腭和后部肌肉软腭,它们在咬合、言语或吞咽方面具有专门的功能。腭的发育受调控似乎是腭前区和后区独特信号和遗传网络的结果。这些区域特异性基因的表达的发育和维持对于正常的腭发育至关重要。许多转录因子和信号通路现在被认为是前(例如,Msx1、Bmp4、Bmp2、Shh、Spry2、Fgf10、Fgf7 和 Shox2)或后特异性(例如,Meox2、Tbx22 和 Barx1)。局部表达和功能清楚地突出了腭在分子水平上的区域模式和分化的重要性。在这里,我们回顾了这些分子途径和网络如何调节次级腭的前-后模式形成和发育。我们假设前腭作为信号中心在建立次级腭的发育中起作用。