Johnson Meshell D, Widdicombe Jonathan H, Allen Lennell, Barbry Pascal, Dobbs Leland G
Department of Medicine, University of California, San Francisco, CA 94143, USA.
Proc Natl Acad Sci U S A. 2002 Feb 19;99(4):1966-71. doi: 10.1073/pnas.042689399. Epub 2002 Feb 12.
Transport of lung liquid is essential for both normal pulmonary physiologic processes and for resolution of pathologic processes. The large internal surface area of the lung is lined by alveolar epithelial type I (TI) and type II (TII) cells; TI cells line >95% of this surface, TII cells <5%. Fluid transport is regulated by ion transport, with water movement following passively. Current concepts are that TII cells are the main sites of ion transport in the lung. TI cells have been thought to provide only passive barrier, rather than active, functions. Because TI cells line most of the internal surface area of the lung, we hypothesized that TI cells could be important in the regulation of lung liquid homeostasis. We measured both Na(+) and K(+) (Rb(+)) transport in TI cells isolated from adult rat lungs and compared the results to those of concomitant experiments with isolated TII cells. TI cells take up Na(+) in an amiloride-inhibitable fashion, suggesting the presence of Na(+) channels; TI cell Na(+) uptake, per microgram of protein, is approximately 2.5 times that of TII cells. Rb(+) uptake in TI cells was approximately 3 times that in TII cells and was inhibited by 10(-4) M ouabain, the latter observation suggesting that TI cells exhibit Na(+)-, K(+)-ATPase activity. By immunocytochemical methods, TI cells contain all three subunits (alpha, beta, and gamma) of the epithelial sodium channel ENaC and two subunits of Na(+)-, K(+)-ATPase. By Western blot analysis, TI cells contain approximately 3 times the amount of alphaENaC/microg protein of TII cells. Taken together, these studies demonstrate that TI cells not only contain molecular machinery necessary for active ion transport, but also transport ions. These results modify some basic concepts about lung liquid transport, suggesting that TI cells may contribute significantly in maintaining alveolar fluid balance and in resolving airspace edema.
肺液的转运对于正常的肺生理过程以及病理过程的消退都至关重要。肺的巨大内表面积由肺泡I型(TI)和II型(TII)上皮细胞覆盖;TI细胞覆盖该表面的>95%,TII细胞<5%。液体转运由离子转运调节,水随之被动移动。目前的观点认为TII细胞是肺中离子转运的主要部位。TI细胞一直被认为仅提供被动屏障功能,而非主动功能。由于TI细胞覆盖肺的大部分内表面积,我们推测TI细胞在肺液稳态调节中可能很重要。我们测量了从成年大鼠肺中分离出的TI细胞中的Na(+)和K(+)(Rb(+))转运,并将结果与同时进行的分离TII细胞实验的结果进行比较。TI细胞以氨氯地平可抑制的方式摄取Na(+),表明存在Na(+)通道;每微克蛋白质的TI细胞Na(+)摄取量约为TII细胞的2.5倍。TI细胞中的Rb(+)摄取量约为TII细胞的3倍,并被10(-4) M哇巴因抑制,后一观察结果表明TI细胞表现出Na(+)-、K(+)-ATP酶活性。通过免疫细胞化学方法,TI细胞含有上皮钠通道ENaC的所有三个亚基(α、β和γ)以及Na(+)-、K(+)-ATP酶的两个亚基。通过蛋白质印迹分析,TI细胞中每微克蛋白质的αENaC含量约为TII细胞的3倍。综上所述,这些研究表明TI细胞不仅含有主动离子转运所需的分子机制,而且还能转运离子。这些结果改变了一些关于肺液转运的基本概念,表明TI细胞可能在维持肺泡液平衡和消退肺泡水肿方面发挥重要作用。