Cardiovascular Research Institute, University of California, San Francisco, San Francisco, United States.
Elife. 2020 May 12;9:e53688. doi: 10.7554/eLife.53688.
Alveolar formation increases the surface area for gas-exchange and is key to the physiological function of the lung. Alveolar epithelial cells, myofibroblasts and endothelial cells undergo coordinated morphogenesis to generate epithelial folds (secondary septa) to form alveoli. A mechanistic understanding of alveologenesis remains incomplete. We found that the planar cell polarity (PCP) pathway is required in alveolar epithelial cells and myofibroblasts for alveologenesis in mammals. Our studies uncovered a cascade that endows cellular properties and novel mechanisms of alveologenesis. This includes PDGF secretion from alveolar type I and type II cells, cell shape changes of type I cells and migration of myofibroblasts. All these cellular properties are conferred by changes in the cytoskeleton and represent a new facet of PCP function. These results extend our current model of PCP signaling from polarizing a field of epithelial cells to conferring new properties at subcellular levels to regulate collective cell behavior.
肺泡形成增加了气体交换的表面积,是肺生理功能的关键。肺泡上皮细胞、肌成纤维细胞和内皮细胞通过协调的形态发生产生上皮褶皱(次级隔膜),形成肺泡。肺泡发生的机制理解仍不完整。我们发现,在哺乳动物中,肺泡上皮细胞和肌成纤维细胞中需要平面细胞极性(PCP)途径才能进行肺泡发生。我们的研究揭示了一个级联反应,赋予了细胞特性和肺泡发生的新机制。这包括 PDGF 从 I 型和 II 型肺泡细胞分泌、I 型细胞形状变化和肌成纤维细胞迁移。所有这些细胞特性都是由细胞骨架的变化赋予的,代表了 PCP 功能的一个新方面。这些结果将我们目前的 PCP 信号模型从极化一个上皮细胞场扩展到赋予亚细胞水平的新特性,以调节细胞的集体行为。