Renal epithelial protein (Apx) is an actin cytoskeleton-regulated Na+ channel

J Biol Chem. 1996 Jul 26;271(30):18045-53. doi: 10.1074/jbc.271.30.18045.

Abstract

Apx, the amphibian protein associated with renal amiloride-sensitive Na+ channel activity and with properties consistent with the pore-forming 150-kDa subunit of an epithelial Na+ channel complex initially purified by Benos et al. (Benos, D. J., Saccomani, G., and Sariban-Sohraby, S.(1987) J. Biol. Chem. 262, 10613-10618), has previously failed to generate amiloride-sensitive Na+ currents (Staub, O., Verrey, F., Kleyman, T. R., Benos, D. J., Rossier, B. C., and Kraehenbuhl, J.-P.(1992) J. Cell Biol. 119, 1497-1506). Renal epithelial Na+ channel activity is tonically inhibited by endogenous actin filaments (Cantiello, H. F., Stow, J., Prat, A. G., and Ausiello, D. A.(1991) Am. J. Physiol. 261, C882-C888). Thus, Apx was expressed and its function examined in human melanoma cells with a defective actin-based cytoskeleton. Apx-transfection was associated with a 60-900% increase in amiloride-sensitive (Ki = 3 microM) Na+ currents. Single channel Na+ currents had a similar functional fingerprint to the vasopressin-sensitive, and actin-regulated epithelial Na+ channel of A6 cells, including a 6-7 pS single channel conductance and a perm-selectivity of Na+:K+ of 4:1. Na+ channel activity was either spontaneous, or induced by addition of actin or protein kinase A plus ATP to the bathing solution of excised inside-out patches. Therefore, Apx may be responsible for the ionic conductance involved in the vasopressin-activated Na+ reabsorption in the amphibian kidney.

Publication types

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

MeSH terms

  • Actins / metabolism*
  • Amiloride / pharmacology
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Biological Transport
  • Cytoskeleton / metabolism*
  • Dose-Response Relationship, Drug
  • Electric Conductivity
  • Epithelium
  • Humans
  • Kidney / metabolism
  • Melanoma
  • Molecular Sequence Data
  • Protein Binding
  • Recombinant Proteins / metabolism
  • Sodium Channels / drug effects
  • Sodium Channels / genetics
  • Sodium Channels / metabolism*
  • Tumor Cells, Cultured
  • Xenopus Proteins*
  • Xenopus laevis

Substances

  • Actins
  • Recombinant Proteins
  • Shroom1 protein, Xenopus
  • Sodium Channels
  • Xenopus Proteins
  • Amiloride