Busch Shana M, Lorenzana Zareeb, Ryan Amy L
Hastings Center for Pulmonary Research, Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Southern California, Los Angeles, CA, United States.
Department of Stem Cell Biology and Regenerative Medicine, University of Southern California, Los Angeles, CA, United States.
Front Pharmacol. 2021 May 12;12:645858. doi: 10.3389/fphar.2021.645858. eCollection 2021.
The extracellular matrix (ECM) is not simply a quiescent scaffold. This three-dimensional network of extracellular macromolecules provides structural, mechanical, and biochemical support for the cells of the lung. Throughout life, the ECM forms a critical component of the pulmonary stem cell niche. Basal cells (BCs), the primary stem cells of the airways capable of differentiating to all luminal cell types, reside in close proximity to the basolateral ECM. Studying BC-ECM interactions is important for the development of therapies for chronic lung diseases in which ECM alterations are accompanied by an apparent loss of the lung's regenerative capacity. The complexity and importance of the native ECM in the regulation of BCs is highlighted as we have yet to create an culture model that is capable of supporting the long-term expansion of multipotent BCs. The interactions between the pulmonary ECM and BCs are, therefore, a vital component for understanding the mechanisms regulating BC stemness during health and disease. If we are able to replicate these interactions in airway models, we could significantly improve our ability to maintain basal cell stemness for use in models and with prospects for cellular therapies. Furthermore, successful, and sustained airway regeneration in an aged or diseased lung by small molecules, novel compounds or via cellular therapy will rely upon both manipulation of the airway stem cells and their immediate niche within the lung. This review will focus on the current understanding of how the pulmonary ECM regulates the basal stem cell function, how this relationship changes in chronic disease, and how replicating native conditions poses challenges for cell culture.
细胞外基质(ECM)并非仅仅是一个静止的支架。这种由细胞外大分子构成的三维网络为肺细胞提供结构、机械和生化支持。在整个生命过程中,ECM构成了肺干细胞微环境的关键组成部分。基底细胞(BCs)是气道的主要干细胞,能够分化为所有腔面细胞类型,它们紧邻基底外侧的ECM。研究BC与ECM的相互作用对于开发慢性肺病的治疗方法很重要,在慢性肺病中,ECM改变伴随着肺再生能力的明显丧失。由于我们尚未创建出能够支持多能BC长期扩增的培养模型,因此天然ECM在调节BC中的复杂性和重要性凸显出来。因此,肺ECM与BC之间的相互作用是理解健康和疾病状态下调节BC干性机制的重要组成部分。如果我们能够在气道模型中复制这些相互作用,我们就能显著提高在模型中维持基底细胞干性以及用于细胞治疗的能力。此外,通过小分子、新型化合物或细胞疗法在衰老或患病肺中成功且持续地实现气道再生将依赖于对气道干细胞及其在肺内直接微环境的操控。本综述将聚焦于目前对肺ECM如何调节基底干细胞功能、这种关系在慢性疾病中如何变化以及复制天然条件对细胞培养带来哪些挑战的理解。