1 Nanoscience and Nanotechnology Research Center, Osaka Prefecture University , Osaka, Japan .
2 Department of Biological Science, Osaka Prefecture University , Osaka, Japan .
Tissue Eng Part C Methods. 2017 Jun;23(6):323-332. doi: 10.1089/ten.TEC.2017.0126. Epub 2017 May 24.
Lung branching morphogenesis has been studied for decades, but the underlying developmental mechanisms are still not fully understood. Cellular movements dynamically change during the branching process, but it is difficult to observe long-term cellular dynamics by in vivo or tissue culture experiments. Therefore, developing an in vitro experimental model of bronchial tree would provide an essential tool for developmental biology, pathology, and systems biology. In this study, we succeeded in reconstructing a bronchial tree in vitro by using primary human bronchial epithelial cells. A high concentration gradient of bronchial epithelial cells was required for branching initiation, whereas homogeneously distributed endothelial cells induced the formation of successive branches. Subsequently, the branches grew in size to the order of millimeter. The developed model contains only two types of cells and it facilitates the analysis of lung branching morphogenesis. By taking advantage of our experimental model, we carried out long-term time-lapse observations, which revealed self-assembly, collective migration with leader cells, rotational motion, and spiral motion of epithelial cells in each developmental event. Mathematical simulation was also carried out to analyze the self-assembly process and it revealed simple rules that govern cellular dynamics. Our experimental model has provided many new insights into lung development and it has the potential to accelerate the study of developmental mechanisms, pattern formation, left-right asymmetry, and disease pathogenesis of the human lung.
肺分支形态发生已经研究了几十年,但潜在的发育机制仍不完全清楚。在分支过程中,细胞的运动是动态变化的,但通过体内或组织培养实验很难观察到长期的细胞动态。因此,开发支气管树的体外实验模型将为发育生物学、病理学和系统生物学提供重要工具。在这项研究中,我们成功地使用原代人支气管上皮细胞在体外重建了支气管树。分支起始需要高浓度的支气管上皮细胞梯度,而均匀分布的内皮细胞则诱导连续分支的形成。随后,分支的大小增长到毫米级。所开发的模型仅包含两种类型的细胞,便于分析肺分支形态发生。利用我们的实验模型,我们进行了长期的延时观察,揭示了上皮细胞在每个发育事件中的自我组装、具有先导细胞的集体迁移、旋转运动和螺旋运动。还进行了数学模拟来分析自组装过程,揭示了控制细胞动力学的简单规则。我们的实验模型为肺发育提供了许多新的见解,并有可能加速人类肺的发育机制、模式形成、左右不对称和疾病发病机制的研究。