Koyama Hiroshi, Shi Dongbo, Suzuki Makoto, Ueno Naoto, Uemura Tadashi, Fujimori Toshihiko
Division of Embryology, National Institute for Basic Biology, Okazaki, Aichi, Japan; SOKENDAI (The Graduate University for Advanced Studies), Hayama, Kanagawa, Japan.
Division of Embryology, National Institute for Basic Biology, Okazaki, Aichi, Japan; Graduate School of Biostudies, Kyoto University, Kyoto, Japan.
Biophys J. 2016 Aug 9;111(3):650-665. doi: 10.1016/j.bpj.2016.06.032.
Epithelia exhibit various three-dimensional morphologies linked to organ function in animals. However, the mechanisms of three-dimensional morphogenesis remain elusive. The luminal epithelium of the mouse oviduct forms well-aligned straight folds along the longitudinal direction of the tubes. Disruption of the Celsr1 gene, a planar cell polarity-related gene, causes ectopically branched folds. Here, we evaluated the mechanical contributions of the epithelium to the fold pattern formation. In the mutant oviduct, the epithelium was more intricate along the longitudinal direction than in the wild-type, suggesting a higher ratio of the longitudinal length of the epithelial layer to that of the surrounding smooth muscle (SM) layer (L-Epi/SM ratio). Our mathematical modeling and computational simulations suggested that the L-Epi/SM ratio could explain the differences in fold branching between the two genotypes. Longitudinal epithelial tensions were increased in well-aligned folds compared with those in disorganized folds both in the simulations and in experimental estimations. Artificially increasing the epithelial tensions suppressed the branching in simulations, suggesting that the epithelial tensions can regulate fold patterning. The epithelial tensions could be explained by the combination of line tensions along the epithelial cell-cell boundaries with the polarized cell arrays observed in vivo. These results suggest that the fold pattern is associated with the polarized cell array through the longitudinal epithelial tension. Further simulations indicated that the L-Epi/SM ratio could contribute to fold pattern diversity, suggesting that the L-Epi/SM ratio is a critical parameter in the fold patterning in tubular organs.
上皮组织呈现出与动物器官功能相关的各种三维形态。然而,三维形态发生的机制仍然不清楚。小鼠输卵管的管腔上皮沿管的纵向形成排列良好的直褶。Celsr1基因(一种与平面细胞极性相关的基因)的破坏会导致异位分支褶皱。在这里,我们评估了上皮组织对褶皱模式形成的力学贡献。在突变的输卵管中,上皮组织沿纵向比野生型更复杂,这表明上皮层的纵向长度与周围平滑肌(SM)层的纵向长度之比(L-Epi/SM比)更高。我们的数学建模和计算模拟表明,L-Epi/SM比可以解释两种基因型之间褶皱分支的差异。在模拟和实验估计中,排列良好的褶皱中的纵向上皮张力都比杂乱褶皱中的高。在模拟中人为增加上皮张力会抑制分支,这表明上皮张力可以调节褶皱模式。上皮张力可以通过沿上皮细胞-细胞边界的线张力与体内观察到的极化细胞阵列的组合来解释。这些结果表明,褶皱模式通过纵向上皮张力与极化细胞阵列相关联。进一步的模拟表明,L-Epi/SM比可能有助于褶皱模式的多样性,这表明L-Epi/SM比是管状器官褶皱模式形成中的一个关键参数。