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Hyaluronic acid is required for palatal shelf movement and its interaction with the tongue during palatal shelf elevation

机译:腭架运动需要透明质酸及其与腭架高度舌头的相互作用

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Palatal shelf elevation is an essential morphogenetic process that results from palatal shelf movement caused by an intrinsic elevating force. The nature of the elevating force remains unclear, but the accumulation of hyaluronic acid (HA) in the extracellular matrix (ECM) of the palatal shelves may play a pivotal role in developing the elevating force. In mammals, HA is synthesized by hyaluronic acid synthases (HAS) that are encoded by three genes (Has1-3). Here, we used the Wnt1-Cre driver to conditionally disrupt hyaluronic acid synthase 2 (Has2) in cranial neural crest cell lineages. All Has2 conditional knockout (cko) mice had cleft palate due to failed shelf elevation during palate development. The HA content was significantly reduced in the craniofacial mesenchyme of Has2 cko mutants. Reduced HA content affected the ECM space and shelf expansion to result in a reduced shelf area and an increased mesenchymal cell density in the palatal shelves of Has2 cko mutants. We examined palatal shelf movement by removal of the tongue and mandible from unfixed E13.5 and early E14.5 embryonic heads. Reduced shelf expansion in Has2 cko mutants altered palatal shelf movement in the medial direction resulting in a larger gap between the palatal shelves than that of littermate controls. We further examined palatal shelf movement in the intact oral cavity by culturing explants containing the maxilla, palate, mandible and tongue (MPMT explants). The palatal shelves elevated alongside morphological changes in the tongue after 24-h culture in MPMT explants of early E14.5 wild type embryos. On the contrary, shelf elevation failed to occur in MPMT explants of age-matched Has2 cko mutants because the tongue obstructs palatal shelf movement, suggesting that reduced shelf expansion could be essential for the palatal shelves to interact with the tongue and overcome tongue obstruction during shelf elevation. Has2 cko mutants also showed micrognathia due to reduced HA content in the mandibular mesenchyme including Meckel’s cartilage. Through 3D imaging and morphometric analysis, we demonstrate that mandibular growth results in a significant increase in the vertical dimension of the common oral-nasal cavity that facilitates palatal shelf movement and its interaction with the tongue during shelf elevation.
机译:腭架升高是一种基本的形态发生过程,由内在升降力引起的腭架运动产生。升降力的性质仍然不清楚,但是腭架的细胞外基质(ECM)中的透明质酸(HA)的积累可能在显影提升力方面发挥枢转作用。在哺乳动物中,通过透明质酸合成(具有)由三种基因(Hase1-3)编码的合成。这里,我们使用WNT1-CRE驱动器在颅神经嵴细胞谱系中有条件地破坏透明质酸合成酶2(HAS2)。所有Hase2有条件淘汰局(CKO)小鼠由于口感开发期间的架子高度而导致腭裂。 HAS2 CKO突变体的颅面间充质细分中,HA含量显着降低。降低的HA含量影响了ECM空间和架子膨胀,以导致具有2 CKO突变体的腭架中的置物面积和增加的间充质细胞密度。我们通过除去舌头和未固定的E13.5和早期的E14.5胚胎头来检查腭架运动。在HAS2 CKO突变体中降低的架子膨胀改变了腭架在内侧方向上的运动,导致腭架与窝夹的较大差距。我们通过培养含有颌骨,腭,下颌骨和舌头(MPMT外植体)的外植体进一步检查了腭架运动。腭架与舌头植物早期E14.5野生型胚胎的MPMT外植体后24小时培养后的形态变化升高。相反,架子抬高未能发生在匹配的Hase2 CKO突变体的MPMT外植物中,因为舌头阻碍了腭架运动,这表明普拉特架子可能是腭架与舌头相互作用并克服舌头障碍物海拔。 Hase2 CKO突变体还显示出MicrognAthia,因为在包括Meckel的软骨的下颌间表单中降低了HA含量。通过3D成像和形态学分析,我们证明下颌生长导致普通口腔腔腔的垂直尺寸的显着增加,这促进了腭架运动及其与钢管抬高期间舌头的相互作用。

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