Inhibitory effect of several sphingolipid metabolites on calcineurin

Neurosci Lett. 2018 Apr 23:673:132-135. doi: 10.1016/j.neulet.2018.03.010. Epub 2018 Mar 7.

Abstract

Neurons have well-developed membrane microdomains called "rafts" that are recovered as a detergent-resistant membrane microdomain fraction (DRM). NAP-22 is one of the major protein components of neuronal DRM. In a previous study, we showed that DRM-derived NAP-22 binds ganglioside and the inhibitory effect of ganglioside to calcineurin (CaN), a neuron-enriched calmodulin-regulated phosphoprotein phosphatase. Considering the important roles of CaN in neurons, identification of other cellular regulators of CaN could be a good clue to understand the molecular background of neuronal function. In this study, we screened the effect of several membrane lipid-derived molecules on the CaN activity and found sphingosine and some sphingosine-derived metabolites such as sphingosylphosphorylcholine, galactosylsphingosine (psychosine), and glucosylsphingosine, have inhibitory effect on CaN through the interaction with calmodulin.

Keywords: Calcineurin; Calmodulin; Glucosylsphingosine; Psychosine; Sphingosylphosphorylcholine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcineurin / metabolism*
  • Calcineurin / pharmacology
  • Calcineurin Inhibitors / metabolism*
  • Calcineurin Inhibitors / pharmacology
  • Escherichia coli
  • Membrane Microdomains / metabolism
  • Sphingolipids / metabolism*
  • Sphingolipids / pharmacology

Substances

  • Calcineurin Inhibitors
  • Sphingolipids
  • Calcineurin