The interaction between endogenous calcineurin and the plasma membrane calcium-dependent ATPase is isoform specific in breast cancer cells

FEBS Lett. 2007 Aug 21;581(21):4115-9. doi: 10.1016/j.febslet.2007.07.054. Epub 2007 Jul 31.

Abstract

Plasma membrane calcium/calmodulin-dependent ATPases (PMCAs) are high affinity calcium pumps that extrude calcium from the cell. Emerging evidence suggests a novel role for PMCAs as regulators of calcium/calmodulin-dependent signal transduction pathways via interaction with specific partner proteins. In this work, we demonstrate that endogenous human PMCA2 and -4 both interact with the signal transduction phosphatase, calcineurin, whereas, no interaction was detected with PMCA1. The strongest interaction was observed between PMCA2 and calcineurin. The domain of PMCA2 involved in the interaction is equivalent to that reported for PMCA4b. PMCA2-calcineurin interaction results in inhibition of the calcineurin/nuclear factor of activated T-cells signalling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / enzymology*
  • Calcineurin / metabolism*
  • Calmodulin / metabolism
  • Cell Line, Tumor
  • Cell Membrane / enzymology*
  • Humans
  • Isoenzymes / metabolism
  • NFATC Transcription Factors / metabolism
  • Neoplasm Proteins / metabolism*
  • Plasma Membrane Calcium-Transporting ATPases / metabolism*
  • Protein Binding
  • Protein Structure, Tertiary
  • Signal Transduction*

Substances

  • Calmodulin
  • Isoenzymes
  • NFATC Transcription Factors
  • Neoplasm Proteins
  • Calcineurin
  • Plasma Membrane Calcium-Transporting ATPases