Extracellular hypotonicity increases Na,K-ATPase cell surface expression via enhanced Na+ influx in cultured renal collecting duct cells

J Am Soc Nephrol. 2004 Oct;15(10):2537-47. doi: 10.1097/01.ASN.0000139931.81844.10.

Abstract

In the renal collecting duct (CD), the Na,K-ATPase, which provides the driving force for Na+ absorption, is under tight multifactorial control. Because CD cells are physiologically exposed to variations of interstitial and tubular fluid osmolarities, the effects of extracellular anisotonicity on Na,K-ATPase cell surface expression were studied. Results show that hypotonic conditions increased, whereas hypertonic conditions had no effect on Na,K-ATPase cell surface expression in confluent mpkCCDcl4 cells. Incubating cells with amphotericin B, which increases [Na+]i, under isotonic or anisotonic conditions, revealed that Na,K-ATPase recruitment to the cell surface was not directly related to variations of cell volume and osmolarity. The effects of amphotericin B and extracellular hypotonicity were not additive, and both were prevented by protein kinase A and proteasome inhibitors, suggesting a common mechanism of action. In line with this hypothesis, extracellular hypotonicity induced a sustained stimulation of the amiloride-sensitive short-circuit current, indicating increased Na+ influx through the apical epithelial Na+ channel. Moreover, inhibiting apical Na+ entry by amiloride, a blocker of epithelial Na+ channel, or incubating cells in Na+ -free medium prevented the cell surface recruitment of Na,K-ATPase in response to extracellular hypotonicity. Altogether, these findings strongly suggest that extracellular hypotonicity stimulates apical Na+ influx leading to increased [Na+]i, protein kinase A activation, and recruitment of Na,K-ATPase units to the cell surface of mpkCCDcl4 cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Biological Transport, Active / physiology*
  • Cation Transport Proteins
  • Cell Membrane / physiology
  • Cell Membrane Permeability
  • Cells, Cultured
  • Enzyme Activation
  • Extracellular Fluid / metabolism*
  • Extracellular Space / metabolism
  • Kidney Tubules, Collecting / cytology
  • Kidney Tubules, Collecting / enzymology*
  • Mice
  • Osmolar Concentration
  • Probability
  • Sensitivity and Specificity
  • Sodium Channels / physiology
  • Sodium-Potassium-Exchanging ATPase / metabolism*
  • Statistics, Nonparametric

Substances

  • Cation Transport Proteins
  • Sodium Channels
  • Adenosine Triphosphatases
  • potassium transporting ATPase
  • Sodium-Potassium-Exchanging ATPase