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首页> 外文期刊>Tissue engineering, Part C. Methods >In Vitro Experimental Model for the Long-Term Analysis of Cellular Dynamics During Bronchial Tree Development from Lung Epithelial Cells
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In Vitro Experimental Model for the Long-Term Analysis of Cellular Dynamics During Bronchial Tree Development from Lung Epithelial Cells

机译:肺上皮细胞支气管树发育期间蜂窝动力学长期分析的体外实验模型

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摘要

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.
机译:几十年来研究了肺部分枝形态发生,但潜在的发展机制仍未完全明白。蜂窝运动在分支过程中动态地改变,但是难以通过体内或组织培养实验观察长期蜂窝动态。因此,开发支气管树的体外实验模型将为发育生物学,病理和系统生物学提供必要的工具。在这项研究中,我们通过使用原发性人支气管上皮细胞成功地重建了支气管树。支气管上皮细胞的高浓度梯度是支气管上皮细胞的支气管上皮细胞,而均匀分布的内皮细胞诱导连续分支的形成。随后,该分支成长为毫米的顺序。开发模型只包含两种类型的细胞,它有助于分析肺分支的形态发生。通过利用我们的实验模型,我们进行了长期延期的观察,揭示了在每个发育事件中的上皮细胞的领导细胞,旋转运动和螺旋运动的自组装,集体迁移。还进行了数学仿真来分析自组装过程,并揭示了控制蜂窝动态的简单规则。我们的实验模型为肺部发展提供了许多新的见解,并且有可能加速人肺的发育机制,模式形成,左右不对称性和疾病发病机制的研究。

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