Department of Anatomy and Cell Biology, Faculty of Medicine, Osaka Medical College, Takatsuki 569-8686, Japan.
Biomed Res Int. 2013;2013:760236. doi: 10.1155/2013/760236. Epub 2013 Feb 12.
Palatogenesis is directed by epithelial-mesenchymal interactions and results partly from remodeling of the extracellular matrix (ECM) of the palatal shelves. Here, we assessed heparanase distribution in developing mouse palates. No heparanase was observed in the vertically oriented palatal shelves in early stages of palate formation. As palate formation progressed, the palatal shelves were reorganized and arranged horizontally above the tongue, and heparanase localized to the epithelial cells of these shelves. When the palatal bilateral shelves first made contact, the heparanase localized to epithelial cells at the tips of shelves. Later in fusing palatal shelves, the cells of the medial epithelial seam (MES) were labeled with intense heparanase signal. In contrast, the basement membrane heparan sulfate (HS) was scarcely observed in the palatal shelves in contact. Moreover, perlecan labeling was sparse in the basement membrane of the MES, on which laminin and type IV collagen were observed. Moreover, we assessed the distribution of matrix metalloproteinase- (MMP-) 9, MMP-2, and MMP-3 in developing mouse palates and these MMPs were observed in the MES. Our findings indicated that heparanase was important for palate formation because it mediated degradation of the ECM of palatal shelves. Heparanase may, in concert with other proteases, participate in the regression of the MES.
腭发生是由上皮-间充质相互作用指导的,部分是由于腭褶细胞外基质 (ECM) 的重塑。在这里,我们评估了肝素酶在发育中的小鼠腭中的分布。在腭形成的早期,垂直定向的腭褶中没有观察到肝素酶。随着腭形成的进展,腭褶被重新组织并水平排列在舌上方,肝素酶定位于这些褶的上皮细胞上。当腭双侧褶首次接触时,肝素酶定位于褶尖端的上皮细胞上。在融合的腭褶中,内侧上皮缝 (MES) 的细胞被强烈的肝素酶信号标记。相比之下,接触的腭褶中几乎没有观察到基底膜硫酸乙酰肝素 (HS)。此外,在 MES 的基底膜上,层粘连蛋白和 IV 型胶原观察到,而 perlecan 标记稀疏。此外,我们评估了基质金属蛋白酶- (MMP-) 9、MMP-2 和 MMP-3 在发育中的小鼠腭中的分布,这些 MMP 在 MES 中观察到。我们的研究结果表明,肝素酶对于腭形成很重要,因为它介导了腭褶 ECM 的降解。肝素酶可能与其他蛋白酶一起参与 MES 的退化。