Yu Kai, Deng Mei, Naluai-Cecchini Theresa, Glass Ian A, Cox Timothy C
Department of Pediatrics, Division of Craniofacial Medicine, University of WashingtonSeattle, WA, USA; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research InstituteSeattle, WA, USA.
Birth Defects Research Laboratory, Department of Pediatrics, University of Washington Seattle, WA, USA.
Front Physiol. 2017 Mar 15;8:154. doi: 10.3389/fphys.2017.00154. eCollection 2017.
Clefting of the secondary palate is one of the most common human birth defects and results from failure of the palatal shelves to fuse during embryonic development. Palatogenesis is traditionally considered to be a highly conserved developmental process among mammalian species. However, cleft palate phenotypes in humans are considerably more variable than those seen in mice, the most common animal model for studying palatal development and pathogenesis of cleft palate. In this investigation, we utilized macroscopic observations, histology and 3D imaging techniques to directly compare palate morphology and the oral-nasal cavity during palate closure in mouse embryos and human conceptuses. We showed that mouse and human palates display distinct morphologies attributable to the structural differences of the oral-nasal cavity. We further showed that the palatal shelves interact differently with the primary palate and nasal septum in the hard palate region and with pharyngeal walls in the soft palate region during palate closure in mice and humans. Knowledge of these morphological differences is important for improved translation of findings in mouse models of human cleft lip/palate and, as such, should ultimately enhance our understanding of human palatal morphogenesis and the pathogenesis of cleft lip/palate in humans.
继发腭裂开是人类最常见的出生缺陷之一,是胚胎发育过程中腭突未能融合所致。传统上认为腭的形成在哺乳动物物种中是一个高度保守的发育过程。然而,人类腭裂的表型比小鼠(研究腭发育和腭裂发病机制最常用的动物模型)的腭裂表型变化大得多。在本研究中,我们利用宏观观察、组织学和三维成像技术,直接比较了小鼠胚胎和人类胎儿腭部闭合过程中腭的形态以及口腔鼻腔情况。我们发现,小鼠和人类的腭呈现出不同的形态,这归因于口腔鼻腔的结构差异。我们还进一步表明,在小鼠和人类腭部闭合过程中,腭突在硬腭区域与原发腭和鼻中隔、在软腭区域与咽壁的相互作用方式不同。了解这些形态差异对于更好地将人类唇腭裂小鼠模型的研究结果进行转化非常重要,因此最终应能增进我们对人类腭形态发生以及人类唇腭裂发病机制的理解。