Matthay M A, Folkesson H G, Verkman A S
Cardiovascular Research Institute, University of California, San Francisco 94143-0130, USA.
Am J Physiol. 1996 Apr;270(4 Pt 1):L487-503. doi: 10.1152/ajplung.1996.270.4.L487.
Substantial progress has been made in understanding the role of the distal airway and alveolar epithelial barriers in regulating lung fluid balance. Molecular, cellular, and whole animal studies have demonstrated that reabsorption of fluid from the distal air spaces of the lung is driven by active sodium transport. Several different in vivo, in situ, and isolated lung preparations have been used to study the mechanisms that regulate fluid transport in the normal and injured lung. Catecholamine-dependent and -independent regulatory mechanisms have been identified that modulate fluid transport, probably by acting on apical sodium channel uptake or the activity of the Na, K-ATPase pumps. Recently, a family of molecular water channels (aquaporins) has been identified that are small (approximately 30 kDa) integral membrane proteins expressed widely in fluid-transporting epithelia and endothelia. At present, four different water channels have been identified in trachea and lung. Measurements of osmotic water permeability in in situ perfused lung and isolated perfused airways suggest a significant contribution of these molecular water channels to measured water permeability. However, further studies are required to determine the role of these water channels in normal pulmonary physiology and disease. Recent studies have provided new insights into the role of the alveolar epithelial barrier in clinical and experimental acute lung injury. Unlike the lung endothelium, the alveolar epithelium is resistant to several clinically relevant types of injury, including endotoxemia and bacteremia as well as aspiration of hyperosmolar solutions. In addition, even when the alveolar barrier has been injured, its capacity to transport edema fluid from the distal air spaces of the lung recovers rapidly. Future studies need to integrate new insights into the molecular mechanisms of alveolar epithelial sodium and water transport with functional studies in the normal and injured lung.
在理解远端气道和肺泡上皮屏障在调节肺液体平衡中的作用方面已取得了重大进展。分子、细胞和整体动物研究表明,肺远端气腔中液体的重吸收是由主动钠转运驱动的。已使用多种不同的体内、原位和离体肺制备方法来研究调节正常和损伤肺中液体转运的机制。已确定了儿茶酚胺依赖性和非依赖性调节机制,这些机制可能通过作用于顶端钠通道摄取或钠钾ATP酶泵的活性来调节液体转运。最近,已鉴定出一个分子水通道家族(水通道蛋白),它们是小的(约30 kDa)整合膜蛋白,广泛表达于液体转运上皮和内皮中。目前,在气管和肺中已鉴定出四种不同的水通道。对原位灌注肺和离体灌注气道中渗透水通透性的测量表明,这些分子水通道对测得的水通透性有重要贡献。然而,需要进一步研究以确定这些水通道在正常肺生理学和疾病中的作用。最近的研究为肺泡上皮屏障在临床和实验性急性肺损伤中的作用提供了新的见解。与肺内皮不同,肺泡上皮对几种临床相关类型的损伤具有抵抗力,包括内毒素血症、菌血症以及高渗溶液的吸入。此外,即使肺泡屏障已受损,其从肺远端气腔转运水肿液的能力也会迅速恢复。未来的研究需要将关于肺泡上皮钠和水转运分子机制的新见解与正常和损伤肺中的功能研究相结合。