The NHE1 Na+/H+ exchanger recruits ezrin/radixin/moesin proteins to regulate Akt-dependent cell survival

J Biol Chem. 2004 Jun 18;279(25):26280-6. doi: 10.1074/jbc.M400814200. Epub 2004 Apr 19.

Abstract

Apoptosis results in cell shrinkage and intracellular acidification, processes opposed by the ubiquitously expressed NHE1 Na(+)/H(+) exchanger. In addition to mediating Na(+)/H(+) transport, NHE1 interacts with ezrin/radixin/moesin (ERM), which tethers NHE1 to cortical actin cytoskeleton to regulate cell shape, adhesion, motility, and resistance to apoptosis. We hypothesize that apoptotic stress activates NHE1-dependent Na(+)/H(+) exchange, and NHE1-ERM interaction is required for cell survival signaling. Apoptotic stimuli induced NHE1-regulated Na(+)/H(+) transport, as demonstrated by ethyl-N-isopropyl-amiloride-inhibitable, intracellular alkalinization. Ectopic NHE1, but not NHE3, expression rescued NHE1-null cells from apoptosis induced by staurosporine or N-ethylmaleimide-stimulated KCl efflux. When cells were subjected to apoptotic stress, NHE1 and phosphorylated ERM physically associated within the cytoskeleton-enriched fraction, resulting in activation of the pro-survival kinase, Akt. NHE1-associated Akt activity and cell survival were inhibited in cells expressing ERM binding-deficient NHE1, dominant negative ezrin constructs, or ezrin mutants with defective binding to phosphoinositide 3-kinase, an upstream regulator of Akt. We conclude that NHE1 promotes cell survival by dual mechanisms: by defending cell volume and pH(i) through Na(+)/H(+) exchange and by functioning as a scaffold for recruitment of a signalplex that includes ERM, phosphoinositide 3-kinase, and Akt.

Publication types

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

MeSH terms

  • Apoptosis
  • Blood Proteins / metabolism*
  • Cell Adhesion
  • Cell Line
  • Cell Survival
  • Cytoskeletal Proteins / metabolism*
  • Cytoskeleton / metabolism
  • Cytosol / metabolism
  • Dose-Response Relationship, Drug
  • Ethylmaleimide / pharmacology
  • Humans
  • Hydrogen-Ion Concentration
  • Immunoblotting
  • Membrane Proteins / metabolism*
  • Microfilament Proteins / metabolism*
  • Models, Biological
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Plasmids / metabolism
  • Potassium Chloride / pharmacology
  • Precipitin Tests
  • Protein Binding
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-akt
  • RNA Interference
  • Signal Transduction
  • Sodium-Hydrogen Exchangers / metabolism
  • Sodium-Hydrogen Exchangers / physiology*
  • Time Factors
  • Transfection
  • Up-Regulation

Substances

  • Blood Proteins
  • Cytoskeletal Proteins
  • Membrane Proteins
  • Microfilament Proteins
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • Sodium-Hydrogen Exchangers
  • ezrin
  • growth factor-activatable Na-H exchanger NHE-1
  • moesin
  • radixin
  • Potassium Chloride
  • AKT1 protein, human
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Ethylmaleimide