Alveolar type 1 cells express the alpha2 Na,K-ATPase, which contributes to lung liquid clearance

Circ Res. 2003 Mar 7;92(4):453-60. doi: 10.1161/01.RES.0000059414.10360.F2. Epub 2003 Jan 30.

Abstract

The alveolar epithelium is composed of alveolar type 1 (AT1) and alveolar type 2 (AT2) cells, which represent approximately 95% and approximately 5% of the alveolar surface area, respectively. Lung liquid clearance is driven by the osmotic gradient generated by the Na,K-ATPase. AT2 cells have been shown to express the alpha1 Na,K-ATPase. We postulated that AT1 cells, because of their larger surface area, should be important in the regulation of active Na+ transport. By immunofluorescence and electron microscopy, we determined that AT1 cells express both the alpha1 and alpha2 Na,K-ATPase isoforms. In isolated, ouabain-perfused rat lungs, the alpha2 Na,K-ATPase in AT1 cells mediated 60% of the basal lung liquid clearance. The beta-adrenergic agonist isoproterenol increased lung liquid clearance by preferentially upregulating the alpha2 Na,K-ATPase protein abundance in the plasma membrane and activity in alveolar epithelial cells (AECs). Rat AECs and human A549 cells were infected with an adenovirus containing the rat Na,K-ATPase alpha2 gene (Adalpha2), which resulted in the overexpression of the alpha2 Na,K-ATPase protein and caused a 2-fold increase in Na,K-ATPase activity. Spontaneously breathing rats were also infected with Adalpha2, which increased alpha2 protein abundance and resulted in a approximately 250% increase in lung liquid clearance. These studies provide the first evidence that alpha2 Na,K-ATPase in AT1 cells contributes to most of the active Na+ transport and lung liquid clearance, which can be further increased by stimulation of the beta-adrenergic receptor or by adenovirus-mediated overexpression of the alpha2 Na,K-ATPase.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cells, Cultured
  • Humans
  • In Situ Hybridization
  • In Vitro Techniques
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Isoproterenol / pharmacology
  • Lung / drug effects
  • Lung / enzymology
  • Lung / metabolism*
  • Male
  • Mice
  • Microscopy, Immunoelectron
  • Ouabain / pharmacology
  • Pulmonary Alveoli / cytology
  • Pulmonary Alveoli / enzymology*
  • Pulmonary Alveoli / ultrastructure
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sodium-Potassium-Exchanging ATPase / genetics
  • Sodium-Potassium-Exchanging ATPase / metabolism*
  • Specific Pathogen-Free Organisms
  • Tumor Cells, Cultured

Substances

  • Isoenzymes
  • RNA, Messenger
  • Ouabain
  • Sodium-Potassium-Exchanging ATPase
  • Isoproterenol