The regulation of neurotransmitter secretion by protein kinase C

Mol Neurobiol. 1998 Oct;18(2):125-55. doi: 10.1007/BF02914269.

Abstract

The effect of protein kinase C (PKC) on the release of neurotransmitters from a number preparations, including sympathetic nerve endings, brain slices, synaptosomes, and neuronally derived cell lines, is considered. A comparison is drawn between effects of activation of PKC on neurotransmitter release from small synaptic vesicles and large dense-cored vesicles. The enhancement of neurotransmitter release is discussed in relation to the effect of PKC on: 1. Rearrangement of the F-actin-based cytoskeleton, including the possible role of MARCKS in this process, to allow access of large dense-cored vesicles to release sites on the plasma membrane. 2. Phosphorylation of key components in the SNAP/SNARE complex associated with the docking and fusion of vesicles at site of secretion. 3. Ion channel activity, particularly Ca2+ channels.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Brain / physiology*
  • Cell Line
  • Cytoskeleton / physiology
  • Homeostasis
  • Humans
  • Intracellular Signaling Peptides and Proteins*
  • Ion Channels / physiology
  • Membrane Proteins*
  • Myristoylated Alanine-Rich C Kinase Substrate
  • Neurons / physiology*
  • Neurotransmitter Agents / metabolism*
  • Protein Kinase C / metabolism*
  • Proteins / metabolism
  • Sympathetic Nervous System / physiology*
  • Synaptosomes / physiology*

Substances

  • Intracellular Signaling Peptides and Proteins
  • Ion Channels
  • MARCKS protein, human
  • Membrane Proteins
  • Neurotransmitter Agents
  • Proteins
  • Myristoylated Alanine-Rich C Kinase Substrate
  • Protein Kinase C