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在生理微流控肺气道模型中闭塞气道再开放过程中上皮损伤与保护。

Epithelium damage and protection during reopening of occluded airways in a physiologic microfluidic pulmonary airway model.

机构信息

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Biomed Microdevices. 2011 Aug;13(4):731-42. doi: 10.1007/s10544-011-9543-5.

Abstract

Airways of the peripheral lung are prone to closure at low lung volumes. Deficiency or dysfunction of pulmonary surfactant during various lung diseases compounds this event by destabilizing the liquid lining of small airways and giving rise to occluding liquid plugs in airways. Propagation of liquid plugs in airways during inflation of the lung exerts large mechanical forces on airway cells. We describe a microfluidic model of small airways of the lung that mimics airway architecture, recreates physiologic levels of pulmonary pressures, and allows studying cellular response to repeated liquid plug propagation events. Substantial cellular injury happens due to the propagation of liquid plugs devoid of surfactant. We show that addition of a physiologic concentration of a clinical surfactant, Survanta, to propagating liquid plugs protects the epithelium and significantly reduces cell death. Although the protective role of surfactants has been demonstrated in models of a propagating air finger in liquid-filled airways, this is the first time to study the protective role of surfactants in liquid plugs where fluid mechanical stresses are expected to be higher than in air fingers. Our parallel computational simulations revealed a significant decrease in mechanical forces in the presence of surfactant, confirming the experimental observations. The results support the practice of providing exogenous surfactant to patients in certain clinical settings as a protective mechanism against pathologic flows. More importantly, this platform provides a useful model to investigate various surface tension-mediated lung diseases at the cellular level.

摘要

外周肺气道在低肺容量时容易关闭。在各种肺部疾病中,肺表面活性物质的缺乏或功能障碍会通过使小气道的液体衬里不稳定并导致气道中闭塞的液体栓子产生,从而使这种情况更加复杂。在肺充气过程中,气道中液体栓子的传播会对气道细胞施加很大的机械力。我们描述了一种模拟气道结构、再现生理水平肺压的肺小气道的微流控模型,并允许研究细胞对反复液体栓子传播事件的反应。由于缺乏表面活性剂的液体栓子的传播,会导致大量细胞损伤。我们表明,向传播的液体栓子中添加生理浓度的临床用表面活性剂 Surfactant(固尔苏)可以保护上皮细胞并显著减少细胞死亡。尽管表面活性剂在充满液体的气道中传播的空气指模型中已经证明了其保护作用,但这是首次研究表面活性剂在液体栓子中的保护作用,因为在液体栓子中预计会比空气指中存在更高的流体力学应力。我们的并行计算模拟显示,在存在表面活性剂的情况下,机械力显著降低,这证实了实验观察结果。这些结果支持在某些临床情况下向患者提供外源性表面活性剂作为针对病理性流动的保护机制的做法。更重要的是,该平台为在细胞水平上研究各种表面张力介导的肺部疾病提供了有用的模型。

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