Ceramide-activated protein kinases A and C zeta inhibit kidney proximal tubule cell Na(+)-ATPase

Arch Biochem Biophys. 2010 Jun 1;498(1):57-61. doi: 10.1016/j.abb.2010.04.004. Epub 2010 Apr 11.

Abstract

The basolateral membranes of kidney proximal tubule cells have (Na(+)+K(+))-ATPase and Na(+)-ATPase activities, involved in Na(+) reabsorption. We showed that ceramide (Cer) modulates protein kinase A (PKA) and protein kinase C (PKC), which are involved in regulating ion transporters. Here we show that ceramide, promotes 60% inhibition of Na(+)-ATPase activity (I(50) approximately 100nM). This effect was completely reversed by inhibiting PKA but did not involve the classic PKC signaling pathway. In these membranes we found the Cer-activated atypical PKC zeta (PKCzeta) isoform. When PKCzeta is inhibited, Cer ceases to inhibit the Na(+)-ATPase, allowing the cAMP/PKA signaling pathway to recover its stimulatory effect on the pump. There were no effects on the (Na(+)+K(+))-ATPase. These results reveal Cer as a potent physiological modulator of the Na(+)-ATPase, participating in a regulatory network in kidney cells and counteracting the stimulatory effect of PKA via PKCzeta.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / antagonists & inhibitors*
  • Animals
  • Cation Transport Proteins / antagonists & inhibitors*
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Ceramides / pharmacology*
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Enzyme Activation / drug effects
  • Kidney Tubules, Proximal / cytology
  • Kidney Tubules, Proximal / drug effects*
  • Kidney Tubules, Proximal / enzymology
  • Kidney Tubules, Proximal / metabolism*
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism*
  • Signal Transduction / drug effects
  • Swine

Substances

  • Cation Transport Proteins
  • Ceramides
  • protein kinase C zeta
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C
  • Adenosine Triphosphatases
  • sodium-translocating ATPase