Protein kinase Cepsilon binds peripherin and induces its aggregation, which is accompanied by apoptosis of neuroblastoma cells

J Biol Chem. 2008 Jun 13;283(24):16653-64. doi: 10.1074/jbc.M710436200. Epub 2008 Apr 11.

Abstract

A hallmark of the afflicted nervous tissue in amyotrophic lateral sclerosis is the presence of protein aggregates, which to a large extent contain the intermediate filament protein peripherin. Here we show that activation of protein kinase C (PKC) or overexpression of PKCepsilon induces the aggregation of peripherin in cultured neuroblastoma cells with elevated amounts of peripherin. The formation of aggregates was coupled to an increased apoptosis, suggesting a functional link between these events. Both induction of aggregates and apoptosis were suppressed in cells that had been transfected with small interfering RNAs targeting PKCepsilon. PKCepsilon and peripherin associate as shown by co-immunoprecipitation, and the interaction is dependent on and mediated by the C1b domain of PKCepsilon. The interaction was specific for PKCepsilon since corresponding structures from other isoforms did not co-precipitate peripherin, with the exception for PKCeta and -, which pulled down minute amounts. PKCepsilon interacts with vimentin through the same structures but does not induce its aggregation. When the PKCepsilon C1b domain is expressed in neuroblastoma cells together with peripherin, both phorbol ester-induced peripherin aggregation and apoptosis are abolished, supporting a model in which PKCepsilon through its interaction with peripherin facilitates its aggregation and subsequent cell death. These events may be prevented by expressing molecules that bind peripherin at the same site as PKCepsilon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Cell Differentiation
  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Intermediate Filament Proteins / chemistry
  • Intermediate Filament Proteins / metabolism*
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / metabolism*
  • Microscopy, Confocal
  • Models, Biological
  • Nerve Tissue Proteins / chemistry
  • Nerve Tissue Proteins / metabolism*
  • Neuroblastoma / metabolism*
  • Peripherins
  • Plasmids / metabolism
  • Protein Binding
  • Protein Isoforms
  • Protein Kinase C-epsilon / metabolism*
  • Transfection
  • Vimentin / metabolism

Substances

  • Intermediate Filament Proteins
  • Membrane Glycoproteins
  • Nerve Tissue Proteins
  • PRPH protein, human
  • Peripherins
  • Protein Isoforms
  • Vimentin
  • Protein Kinase C-epsilon