Bornert Fabien, Choquet Philippe, Gros Catherine I, Aubertin Gaelle, Perrin-Schmitt Fabienne, Clauss François, Lesot Hervé, Constantinesco André, Schmittbuhl Matthieu
Institut National de la Santé et de la Recherche Médicale, INSERM UMR 977, University of Strasbourg Strasbourg, France.
Front Physiol. 2011 Apr 20;2:15. doi: 10.3389/fphys.2011.00015. eCollection 2011.
X-linked hypohidrotic ectodermal dysplasia (XLHED) is a genetic disorder due to a mutation of the EDA gene and is mainly characterized by an impaired formation of hair, teeth and sweat glands, and craniofacial dysmorphologies. Although tooth abnormalities in Tabby (Ta) mutant mice - the murine model of XLHED - have been extensively studied, characterization of the craniofacial complex, and more specifically the mandibular morphology has received less attention. From 3D micro-CT reconstructions of the left mandible, the mandibular outline observed in lateral view, was quantified using 2D elliptical Fourier analysis. Comparisons between Ta specimens and their wild-type controls were carried out showing significant shape differences between mouse strains enabling a clear distinction between hemizygous Ta specimens and the other mouse groups (WT and heterozygous Eda(Ta/+) specimens). Morphological differences associated with HED correspond not only to global mandibular features (restrained development of that bone along dorsoventral axis), but also to subtle aspects such as the marked backward projection of the coronoid process or the narrowing of the mandibular condylar neck. These modifications provide for the first time, evidence of a predominant effect of the Ta mutation on the mandibular morphology. These findings parallel the well described abnormalities of jugal tooth row and skeletal defects in Ta mice, and underline the role played by EDA-A in the reciprocal epithelial-mesenchymal interactions that are of critical importance in normal dental and craniofacial development.
X连锁低汗性外胚层发育不良(XLHED)是一种由EDA基因突变引起的遗传性疾病,主要特征为毛发、牙齿和汗腺形成受损以及颅面部畸形。尽管作为XLHED小鼠模型的虎斑(Ta)突变小鼠的牙齿异常已得到广泛研究,但颅面部复合体,尤其是下颌形态的特征描述却较少受到关注。通过对左下颌骨的三维显微CT重建,利用二维椭圆傅里叶分析对侧视图中观察到的下颌轮廓进行了量化。对Ta标本与其野生型对照进行了比较,结果显示小鼠品系之间存在显著的形状差异,从而能够明确区分半合子Ta标本与其他小鼠组(野生型和杂合子Eda(Ta/+)标本)。与低汗性外胚层发育不良相关的形态学差异不仅对应于整体下颌特征(该骨沿背腹轴的发育受限),还对应于细微方面,如冠状突明显向后突出或下颌髁突颈部变窄。这些改变首次提供了Ta突变对下颌形态具有主要影响的证据。这些发现与Ta小鼠中描述详尽的颧牙列异常和骨骼缺陷相平行,并强调了EDA-A在正常牙齿和颅面发育中至关重要的上皮-间充质相互作用中所起的作用。