Ishida Sumire, Tanaka Ryosuke, Yamaguchi Naoya, Ogata Genki, Mizutani Takeomi, Kawabata Kazushige, Haga Hisashi
Transdisciplinary Life Science Course, Faculty of Advanced Life Science, Hokkaido University, Sapporo, Japan.
Transdisciplinary Life Science Course, Faculty of Advanced Life Science, Hokkaido University, Sapporo, Japan; Research Center for Cooperative Projects, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
PLoS One. 2014 Aug 29;9(8):e99655. doi: 10.1371/journal.pone.0099655. eCollection 2014.
Lumen formation is important for morphogenesis; however, an unanswered question is whether it involves the collective migration of epithelial cells. Here, using a collagen gel overlay culture method, we show that Madin-Darby canine kidney cells migrated collectively and formed a luminal structure in a collagen gel. Immediately after the collagen gel overlay, an epithelial sheet folded from the periphery, migrated inwardly, and formed a luminal structure. The inhibition of integrin-β1 or Rac1 activity decreased the migration rate of the peripheral cells after the sheets folded. Moreover, lumen formation was perturbed by disruption of apical-basolateral polarity induced by transforming growth factor-β1. These results indicate that cell migration and cell polarity play an important role in folding. To further explore epithelial sheet folding, we developed a computer-simulated mechanical model based on the rigidity of the extracellular matrix. It indicated a soft substrate is required for the folding movement.
管腔形成对形态发生很重要;然而,一个尚未解决的问题是它是否涉及上皮细胞的集体迁移。在这里,我们使用胶原凝胶覆盖培养方法,证明了Madin-Darby犬肾细胞在胶原凝胶中集体迁移并形成管腔结构。在胶原凝胶覆盖后,上皮片层立即从周边折叠,向内迁移,并形成管腔结构。整合素-β1或Rac1活性的抑制降低了片层折叠后周边细胞的迁移速率。此外,转化生长因子-β1诱导的顶-基极性破坏扰乱了管腔形成。这些结果表明细胞迁移和细胞极性在折叠过程中起重要作用。为了进一步探索上皮片层折叠,我们基于细胞外基质的刚性开发了一个计算机模拟力学模型。结果表明折叠运动需要柔软的底物。