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Alveolar Fluid Clearance in Pathologically Relevant Conditions: In Vitro and In Vivo Models of Acute Respiratory Distress Syndrome

机译:病理相关情况下的肺泡液清除:急性呼吸窘迫综合征的体外和体内模型。

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摘要

Critically ill patients with respiratory failure from acute respiratory distress syndrome (ARDS) have reduced ability to clear alveolar edema fluid. This reduction in alveolar fluid clearance (AFC) contributes to the morbidity and mortality in ARDS. Thus, it is important to understand why AFC is reduced in ARDS in order to design targeted therapies. In this review, we highlight experiments that have advanced our understanding of ARDS pathogenesis, with particular reference to the alveolar epithelium. First, we review how vectorial ion transport drives the clearance of alveolar edema fluid in the uninjured lung. Next, we describe how alveolar edema fluid is less effectively cleared in lungs affected by ARDS and describe selected in vitro and in vivo experiments that have elucidated some of the molecular mechanisms responsible for the reduced AFC. Finally, we describe one potential therapy that targets this pathway: bone marrow-derived mesenchymal stem (stromal) cells (MSCs). Based on preclinical studies, MSCs enhance AFC and promote the resolution of pulmonary edema and thus may offer a promising cell-based therapy for ARDS.
机译:患有急性呼吸窘迫综合征(ARDS)的呼吸衰竭的重症患者清除肺泡水肿液的能力降低。肺泡液清除率(AFC)的下降有助于ARDS的发病率和死亡率。因此,重要的是要理解为什么ARDS中的AFC减少才能设计出针对性的疗法。在这篇综述中,我们重点介绍了对ARDS发病机制有更深入了解的实验,特别是针对肺泡上皮的实验。首先,我们回顾了矢量离子传输如何驱动未损伤肺中肺泡水肿液的清除。接下来,我们描述了如何在受ARDS影响的肺部清除肺泡水肿液的效率降低,并描述了选定的体外和体内实验,这些实验阐明了导致AFC降低的某些分子机制。最后,我们描述了一种靶向该途径的潜在疗法:骨髓来源的间充质干(基质)细胞(MSC)。根据临床前研究,MSC可增强AFC并促进肺水肿的消退,因此可能为ARDS提供有希望的基于细胞的疗法。

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