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小鼠腭发育模型中舌体影响腭板抬升模式的表征分析

Characterization of the Effect of Tongue on Palatal Shelf Elevation Patterns in a Mouse Model of Palatogenesis

  • 摘要:
    目的 研究哺乳动物的腭发育中腭板抬升模式在前后区域差异的决定机制。
    方法 以小鼠腭发育为模型,将抬升前(E13.5早期)、抬升中(E13.5晚期)和抬升后(E14.5早期)的腭板进行冠状向多平面切片,HE染色对比腭和舌的形态变化及空间关联,肌球蛋白重链1(myosin heavy chain 1, MYH1,存在于慢肌纤维中,负责肌肉的收缩和运动)免疫荧光染色观察腭不同抬升阶段舌肌发育成熟特征;通过腭器官体外培养试验,HE染色观察E13.5早期无舌情况下腭板抬升模式变化;通过胞外基质肌腱蛋白C(Tenascin-C)表达检测(免疫荧光染色),验证舌对前后份腭板抬升模式差异的影响。
    结果 切片HE染色结果显示,在腭抬升期从后到前份,舌冠状向高度下降,侧向倾斜加强且变扁平,但舌矢状向伸长,腭板的抬升模式从缓慢重塑转变为快速翻折,MYH1在此时期大量表达于舌内外肌束。体外腭器官培养发现:无舌条件下,腭板后份抬升未形成新的舌侧凸起,Tenascin-C的区域表达与上抬前一致,腭后份抬升类似于前份抬升模式。
    结论 舌体可能是腭板后份形态重塑抬升模式形成的重要影响因素。

     

    Abstract:
    Objective To investigate the mechanisms underlying regional heterogeneity in the elevating patterns of palatal shelf during mammalian craniofacial development.
    Methods Using a mouse model of embryonic palatal development, we acquired coronal multi-plane slices of the palatal shelves before elevation (early E13.5), during elevation (late E13.5), and after elevation (early E14.5). Hematoxylin and eosin (HE) staining was performed to compare the morphological changes and spatial correlations between the palate and tongue. Immunofluorescence staining of myosin heavy chain 1 (MYH1), a marker found in slow muscle fibers and responsible for muscle contraction and movement, was performed to observe the tongue muscle development characteristics at different stages. We also observed changes in the palatal shelf elevating patterns at early E13.5 in the absence of the tongue through HE-stained in vitro palate organ culture. Further immunofluorescence staining of tenascin-C, an extracellular matrix protein, was performed to evaluate the effect of the tongue on the elevating pattern of the palatal shelf along the anterior-posterior axis.
    Results HE staining results of the coronal multi-plane slices showed that during the elevation period, from the posterior toward anterior, the coronal height of the tongue decreased, lateral inclination and flattening increased, but the sagittal length of the tongue increased. The elevating pattern of the palatal shelf changed from slow remodeling to rapid flipping, and MYH1 was abundantly expressed in both the internal and external muscle bundles of the tongue during this period. According to findings from in vitro cultivation of palatal organs, the posterior part of the palatal shelf elevated without forming new lateral lingual protrusions in the absence of the tongue. The regional expression pattern of tenascin-C was consistent with that observed before elevation. The posterior palate exhibited an elevation pattern similar to that of the anterior region.
    Conclusion The tongue may play a crucial role in shaping the posterior morphological remodeling and distinct elevation patterns of the palatal shelf.

     

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