Spines and neurite branches function as geometric attractors that enhance protein kinase C action. Academic Article uri icon

Overview

abstract

  • Ca2+ and diacylglycerol-regulated protein kinase Cs (PKCs; conventional PKC isoforms, such as PKCgamma) are multifunctional signaling molecules that undergo reversible plasma membrane translocation as part of their mechanism of activation. In this article, we investigate PKCgamma translocation in hippocampal neurons and show that electrical or glutamate stimulation leads to a striking enrichment of PKCgamma in synaptic spines and dendritic branches. Translocation into spines and branches was delayed when compared with the soma plasma membrane, and PKCgamma remained in these structures for a prolonged period after the response in the soma ceased. We have developed a quantitative model for the translocation process by measuring the rate at which PKCgamma crossed the neck of spines, as well as cytosolic and membrane diffusion coefficients of PKCgamma. Our study suggests that neurons make use of a high surface-to-volume ratio of spines and branches to create a geometric attraction process for PKC that imposes a delayed enhancement of PKC action at synapses and in peripheral processes.

publication date

  • September 26, 2005

Research

keywords

  • Dendritic Spines
  • Neurites
  • Protein Kinase C

Identity

PubMed Central ID

  • PMC2171530

Scopus Document Identifier

  • 25444521521

Digital Object Identifier (DOI)

  • 10.1083/jcb.200503118

PubMed ID

  • 16186260

Additional Document Info

volume

  • 170

issue

  • 7