Influence of MPP+ on the state of tubulin polymerisation in NGF-differentiated PC12 cells

J Neurosci Res. 1999 Apr 1;56(1):28-35. doi: 10.1002/(SICI)1097-4547(19990401)56:1<28::AID-JNR4>3.0.CO;2-2.

Abstract

Cytoskeletal proteins have been reported as constituents of cytoplasmic inclusions typical of degenerated neurones in Parkinson's disease and, in addition, the involvement of cytoskeleton in the mechanism of action of the parkinsonism-producing neurotoxin MPP+ is emerging. Here we investigate the influence of MPP+ on the dynamic behaviour of microtubules. Neurone-like cells derived from a rat pheochromocytoma cell line (PC12) and differentiated with nerve growth factor are used as a model system. We found that sublethal doses of the neurotoxin markedly affect the state of tubulin polymerisation: polymerised tubulins significantly decreased, whereas an increase of unpolymerised alpha-tubulin was observed. Since the concentration of unassembled tubulin directly regulates tubulin synthesis by a feedback mechanism, we studied alpha- and beta-tubulin synthesis by metabolic labelling of PC12 cells with [35S] methionine and following immunoprecipitations. The results showed the significant decrease of labelling in both the microtubule subunits in cells exposed to the neurotoxin. We suggest that the MPP+-induced imbalance of tubulin polymerisation and synthesis represents a novel early step in the mechanism of action of the neurotoxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenylpyridinium / pharmacology*
  • Animals
  • Cell Differentiation / physiology*
  • Fluorescent Antibody Technique, Indirect
  • Kinetics
  • Macromolecular Substances
  • Microtubules / drug effects*
  • Microtubules / physiology
  • Nerve Growth Factors / pharmacology
  • Neurotoxins / pharmacology
  • PC12 Cells
  • Rats
  • Tubulin / biosynthesis
  • Tubulin / drug effects*
  • Tubulin / metabolism

Substances

  • Macromolecular Substances
  • Nerve Growth Factors
  • Neurotoxins
  • Tubulin
  • 1-Methyl-4-phenylpyridinium