Takigawa Toshiya, Shiota Kohei
Department of Anatomy and Developmental Biology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Int J Dev Biol. 2004 Jun;48(4):307-17. doi: 10.1387/ijdb.041840tt.
During fusion of the mammalian secondary palate, it has been suggested that palatal medial edge epithelial (MEE) cells disappear by means of apoptosis, epithelial-mesenchymal transformation (EMT) and epithelial cell migration. However, it is widely believed that MEE cells never differentiate unless palatal shelves make contact and the midline epithelial seam is formed. In order to clarify the potential of MEE cells to differentiate, we cultured single (unpaired) palatal shelves of ICR mouse fetuses by using suspension and static culture methods with two kinds of gas-mixtures. We thereby found that MEE cells can disappear throughout the medial edge even without contact and adhesion to the opposing MEE in suspension culture with 95% O2/5% CO2. Careful examination of MEE cell behavior in the culture revealed that apoptosis, EMT, and epithelial cell migration all occurred at various stages of MEE cell disappearance, including the transient formation and disappearance of epithelial triangles and islets. In contrast, MEE cells showed poor differentiation in static culture in a CO2 incubator. Furthermore, mouse and human amniotic fluids were found to prevent MEE cell differentiation in the cultured single palatal shelf, although paired palatal shelves fused successfully even in the presence of amniotic fluid. We therefore conclude that terminal differentiation of MEE cells is not necessarily dependent on palatal shelf contact and midline epithelial seam formation, but such MEE cell differentiation appears to be prevented in utero by amniotic fluid unless palatal shelves make close contact and the midline epithelial seam is formed.
在哺乳动物次生腭融合过程中,有人提出腭内侧边缘上皮(MEE)细胞通过凋亡、上皮-间充质转化(EMT)和上皮细胞迁移而消失。然而,人们普遍认为,除非腭突相互接触并形成中线上皮缝,MEE细胞不会分化。为了阐明MEE细胞分化的潜力,我们采用悬浮培养和静态培养方法,使用两种气体混合物,对ICR小鼠胎儿的单个(未配对)腭突进行培养。由此我们发现,在含95% O2/5% CO2的悬浮培养中,即使没有与相对的MEE细胞接触和黏附,MEE细胞也能在整个内侧边缘消失。对培养中MEE细胞行为的仔细观察表明,凋亡、EMT和上皮细胞迁移均发生在MEE细胞消失的各个阶段,包括上皮三角形和小岛的短暂形成和消失。相比之下,在二氧化碳培养箱中的静态培养中,MEE细胞分化较差。此外,发现小鼠和人类羊水可阻止培养的单个腭突中MEE细胞的分化,尽管即使存在羊水,配对的腭突也能成功融合。因此,我们得出结论,MEE细胞的终末分化不一定依赖于腭突接触和中线上皮缝的形成,但除非腭突紧密接触并形成中线上皮缝,否则这种MEE细胞分化似乎在子宫内会被羊水阻止。