Department of Pediatrics, Division of Newborn Medicine, Boston Children's Hospital, Boston, MA, 02115, USA.
Department of Pediatrics, Division of Hematology/Oncology, Stem Cell Program; Boston Children's Hospital, Boston, MA, 02115, USA.
Sci Rep. 2019 Apr 23;9(1):6479. doi: 10.1038/s41598-019-42819-1.
Lung epithelial cell damage and dysfunctional repair play a role in the development of lung disease. Effective repair likely requires the normal functioning of alveolar stem/progenitor cells. For example, we have shown in a mouse model of bronchopulmonary dysplasia (BPD) that mesenchymal stem cells (MSC) protect against hyperoxic lung injury at least in part by increasing the number of Epcam Sca-1 distal lung epithelial cells. These cells are capable of differentiating into both small airway (CCSP) and alveolar (SPC) epithelial cells in three-dimensional (3D) organoid cultures. To further understand the interactions between MSC and distal lung epithelial cells, we added MSC to lung progenitor 3D cultures. MSC stimulated Epcam Sca-1 derived organoid formation, increased alveolar differentiation and decreased self-renewal. MSC-conditioned media was sufficient to promote alveolar organoid formation, demonstrating that soluble factors secreted by MSC are likely responsible for the response. This work provides strong evidence of a direct effect of MSC-secreted factors on lung progenitor cell differentiation.
肺上皮细胞损伤和功能障碍修复在肺部疾病的发展中起作用。有效的修复可能需要肺泡干细胞/祖细胞的正常功能。例如,我们在支气管肺发育不良(BPD)的小鼠模型中表明,间充质干细胞(MSC)通过增加 Epcam Sca-1 远端肺上皮细胞的数量来至少部分保护免受高氧肺损伤。这些细胞能够在三维(3D)类器官培养物中分化为小气道(CCSP)和肺泡(SPC)上皮细胞。为了进一步了解 MSC 和远端肺上皮细胞之间的相互作用,我们将 MSC 添加到肺祖细胞 3D 培养物中。MSC 刺激 Epcam Sca-1 衍生的类器官形成,增加肺泡分化并减少自我更新。MSC 条件培养基足以促进肺泡类器官的形成,表明 MSC 分泌的可溶性因子可能是导致这种反应的原因。这项工作为 MSC 分泌因子对肺祖细胞分化的直接影响提供了强有力的证据。