Cyclin-dependent kinase 5 associated with p39 promotes Munc18-1 phosphorylation and Ca(2+)-dependent exocytosis

J Biol Chem. 2004 Jul 9;279(28):29534-41. doi: 10.1074/jbc.M312711200. Epub 2004 Apr 26.

Abstract

Cyclin-dependent kinase 5 (Cdk5) is a proline-directed serine/threonine protein kinase that requires association with a regulatory protein, p35 or p39, to form an active enzyme. Munc18-1 plays an essential role in membrane fusion, and its function is regulated by phosphorylation. We report here that both p35 and p39 were expressed in insulin-secreting beta-cells, where they exhibited individual subcellular distributions and associated with membranous organelles of different densities. Overexpression of Cdk5, p35, or p39 showed that Cdk5 and p39 augmented Ca(2+)-induced insulin exocytosis. Suppression of p39 and Cdk5, but not of p35, by antisense oligonucleotides selectively inhibited insulin exocytosis. Transient transfection of primary beta-cells with Munc18-1 templates mutated in potential Cdk5 or PKC phosphorylation sites, in combination with Cdk5 and the different Cdk5 activators, suggested that Cdk5/p39-promoted Ca(2+)-dependent insulin secretion from primary beta-cells by phosphorylating Munc18-1 at a biochemical step immediately prior to vesicle fusion.

Publication types

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

MeSH terms

  • Animals
  • Brain / metabolism
  • Calcium / metabolism*
  • Cells, Cultured
  • Cyclin-Dependent Kinase 5
  • Cyclin-Dependent Kinases / genetics
  • Cyclin-Dependent Kinases / metabolism*
  • Enzyme Activation
  • Exocytosis / physiology*
  • Female
  • Human Growth Hormone / metabolism
  • Humans
  • Insulin / metabolism
  • Islets of Langerhans / cytology
  • Islets of Langerhans / metabolism
  • Membrane Potentials / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • Munc18 Proteins
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Oligonucleotides, Antisense / metabolism
  • Patch-Clamp Techniques
  • Phosphorylation
  • Subcellular Fractions / metabolism
  • Vesicular Transport Proteins / genetics
  • Vesicular Transport Proteins / metabolism*

Substances

  • Cdk5 activator p39
  • Insulin
  • Munc18 Proteins
  • Nerve Tissue Proteins
  • Oligonucleotides, Antisense
  • STXBP1 protein, human
  • Stxbp1 protein, mouse
  • Vesicular Transport Proteins
  • neuronal Cdk5 activator (p25-p35)
  • Human Growth Hormone
  • Cyclin-Dependent Kinase 5
  • CDK5 protein, human
  • Cdk5 protein, mouse
  • Cyclin-Dependent Kinases
  • Calcium