Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, The Davis Heart and Lung Research Institute, The Ohio State University, Wexner Medical Center, 473 West 12th Avenue, Columbus, OH 43210.
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, The Davis Heart and Lung Research Institute, The Ohio State University, Wexner Medical Center, 473 West 12th Avenue, Columbus, OH 43210; Department of Biomedical Engineering, The Ohio State University, 2124N Fontana Labs, 140 West 19th Avenue, Columbus, OH 43210.
J Biomech Eng. 2021 Nov 1;143(11). doi: 10.1115/1.4051118.
Cells within the lung micro-environment are continuously subjected to dynamic mechanical stimuli which are converted into biochemical signaling events in a process known as mechanotransduction. In pulmonary diseases, the abrogated mechanical conditions modify the homeostatic signaling which influences cellular phenotype and disease progression. The use of in vitro models has significantly expanded our understanding of lung mechanotransduction mechanisms. However, our ability to match complex facets of the lung including three-dimensionality, multicellular interactions, and multiple simultaneous forces is limited and it has proven difficult to replicate and control these factors in vitro. The goal of this review is to (a) outline the anatomy of the pulmonary system and the mechanical stimuli that reside therein, (b) describe how disease impacts the mechanical micro-environment of the lung, and (c) summarize how existing in vitro models have contributed to our current understanding of pulmonary mechanotransduction. We also highlight critical needs in the pulmonary mechanotransduction field with an emphasis on next-generation devices that can simulate the complex mechanical and cellular environment of the lung. This review provides a comprehensive basis for understanding the current state of knowledge in pulmonary mechanotransduction and identifying the areas for future research.
肺部微环境中的细胞不断受到动态机械刺激,这些刺激在一个称为机械转导的过程中转化为生化信号事件。在肺部疾病中,机械条件的改变会改变稳态信号,从而影响细胞表型和疾病进展。体外模型的使用极大地扩展了我们对肺机械转导机制的理解。然而,我们匹配肺部包括三维结构、多细胞相互作用和多个同时力等复杂方面的能力有限,并且在体外复制和控制这些因素一直具有挑战性。本篇综述的目的是:(a)概述肺部系统的解剖结构和存在于其中的机械刺激;(b)描述疾病如何影响肺部的机械微环境;(c)总结现有的体外模型如何促进我们对肺机械转导的理解。我们还强调了肺部机械转导领域的关键需求,重点介绍了能够模拟肺部复杂机械和细胞环境的下一代设备。这篇综述为理解肺机械转导的现有知识状态以及确定未来研究领域提供了全面的基础。