Nizamoglu Mehmet, Burgess Janette K
University of Groningen, University Medical Center Groningen, Department of Pathology and Medical Biology, Groningen, Netherlands.
University of Groningen, University Medical Center Groningen, Groningen Research Institute for Asthma and COPD (GRIAC), Groningen, Netherlands.
Front Pharmacol. 2023 Mar 9;14:1154193. doi: 10.3389/fphar.2023.1154193. eCollection 2023.
Disruption of the complex interplay between cells and extracellular matrix (ECM), the scaffold that provides support, biochemical and biomechanical cues, is emerging as a key element underlying lung diseases. We readily acknowledge that the lung is a flexible, relatively soft tissue that is three dimensional (3D) in structure, hence a need exists to develop model systems that reflect these properties. Lung ECM-derived hydrogels have recently emerged as a model system that mimics native lung physiology; they contain most of the plethora of biochemical components in native lung, as well as reflecting the biomechanics of native tissue. Research investigating the contribution of cell:matrix interactions to acute and chronic lung diseases has begun adopting these models but has yet to harness their full potential. This perspective article provides insight about the latest advances in the development, modification, characterization and utilization of lung ECM-derived hydrogels. We highlight some opportunities for expanding research incorporating lung ECM-derived hydrogels and potential improvements for the current approaches. Expanding the capabilities of investigations using lung ECM-derived hydrogels is positioned at a cross roads of disciplines, the path to new and innovative strategies for unravelling disease underlying mechanisms will benefit greatly from interdisciplinary approaches. While challenges need to be addressed before the maximum potential can be unlocked, with the rapid pace at which this field is evolving, we are close to a future where faster, more efficient and safer drug development targeting the disrupted 3D microenvironment is possible using lung ECM-derived hydrogels.
细胞与细胞外基质(ECM)之间复杂的相互作用遭到破坏,而细胞外基质是提供支持、生化和生物力学信号的支架,这正成为肺部疾病的一个关键潜在因素。我们欣然承认,肺是一种结构上三维(3D)的、柔软且具有弹性的组织,因此需要开发能够反映这些特性的模型系统。源自肺ECM的水凝胶最近作为一种模拟天然肺生理的模型系统出现;它们包含天然肺中大量的生化成分,同时也反映了天然组织的生物力学特性。研究细胞与基质相互作用对急性和慢性肺部疾病的影响已开始采用这些模型,但尚未充分发挥其潜力。这篇观点文章阐述了源自肺ECM的水凝胶在开发、修饰、表征和应用方面的最新进展。我们强调了一些扩展利用源自肺ECM的水凝胶进行研究的机会以及对当前方法的潜在改进。扩展使用源自肺ECM的水凝胶进行研究的能力处于多学科的交叉点,采用跨学科方法将极大地有助于找到揭示疾病潜在机制的新的创新策略。虽然在释放其最大潜力之前还需要应对一些挑战,但鉴于该领域的快速发展,我们已接近这样一个未来:利用源自肺ECM的水凝胶有可能实现针对破坏的3D微环境更快、更高效且更安全的药物开发。