The calcineurin-dynamin 1 complex as a calcium sensor for synaptic vesicle endocytosis

J Biol Chem. 1999 Sep 10;274(37):25963-6. doi: 10.1074/jbc.274.37.25963.

Abstract

Exocytosis of synaptic vesicles is calcium-dependent, with synaptotagmin serving as the calcium sensor. Endocytosis of synaptic vesicles has also been postulated as a calcium-dependent process; however, an endocytic calcium sensor has not been found. We now report a physical association between the calcium-dependent phosphatase calcineurin and dynamin 1, a component of the synaptic endocytic machinery. The calcineurin-dynamin 1 interaction is calcium-dependent, with an EC(50) for calcium in the range of 0.1-0. 4 microM. Disruption of the calcineurin-dynamin 1 interaction inhibits clathrin-mediated endocytosis. Thus, the calcium-dependent formation of the calcineurin-dynamin 1 complex, delivered to the other endocytic coat proteins, provides a calcium-sensing mechanism that facilitates endocytosis.

Publication types

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

MeSH terms

  • Animals
  • Calcineurin / metabolism*
  • Calcium / metabolism*
  • Clathrin / antagonists & inhibitors
  • Clathrin / metabolism
  • Dynamin I
  • Dynamins
  • Endocytosis*
  • GTP Phosphohydrolases / metabolism*
  • Glutathione Transferase / metabolism
  • Humans
  • Immunophilins / metabolism
  • Rats
  • Recombinant Fusion Proteins / metabolism
  • Synaptic Vesicles / metabolism*
  • Tacrolimus Binding Proteins

Substances

  • Clathrin
  • Recombinant Fusion Proteins
  • Glutathione Transferase
  • Calcineurin
  • Dynamin I
  • GTP Phosphohydrolases
  • Dynamins
  • Tacrolimus Binding Proteins
  • Immunophilins
  • Calcium