nm23 influences proliferation and differentiation of PC12 cells in response to nerve growth factor

Cell Growth Differ. 1996 Dec;7(12):1689-95.

Abstract

The nm23 genes codify nucleoside diphosphate kinases, which have been shown to be involved in the regulation of microtubule dynamics. We have demonstrated previously that the association between the Nm23-M1 protein and cytoskeletal beta-tubulin correlates with cell differentiation. It is known that microtubules and microtubule-associated proteins are fundamental elements regulating neuronal differentiation. In the present study, we have investigated the ability of nm23 to influence nerve growth factor-induced PC12 cell differentiation. To this end, we have altered PC12 intracellular levels of nm23-M1 by means of sense and antisense transfections. In the presence of nerve growth factor, overexpression of nm23 delays cell cycle transition, rapidly induces neurite outgrowth, and increases the expression of neurofilament and microtubule proteins. On the contrary, down-regulation of nm23 enhances cell proliferation and inhibits neuronal differentiation. These findings indicate that neuronal cell proliferation and differentiation can be modulated by nm23 expression levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Cycle / drug effects
  • Cell Cycle / physiology
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cell Division / drug effects
  • Cell Division / physiology
  • Cytoskeleton / chemistry
  • Cytoskeleton / metabolism
  • DNA / metabolism
  • DNA, Complementary / genetics
  • Flow Cytometry
  • Gene Expression Regulation, Enzymologic / physiology
  • Kinetics
  • Monomeric GTP-Binding Proteins*
  • NM23 Nucleoside Diphosphate Kinases
  • Nerve Growth Factors / pharmacology*
  • Neurites / drug effects
  • Neurites / physiology
  • Neurofilament Proteins / analysis
  • Neurofilament Proteins / metabolism
  • Nucleoside-Diphosphate Kinase / genetics*
  • Nucleoside-Diphosphate Kinase / metabolism
  • PC12 Cells / cytology
  • PC12 Cells / enzymology
  • PC12 Cells / ultrastructure
  • RNA, Antisense
  • Rats
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transfection
  • Tubulin / analysis
  • Tubulin / metabolism

Substances

  • DNA, Complementary
  • NM23 Nucleoside Diphosphate Kinases
  • Nerve Growth Factors
  • Neurofilament Proteins
  • RNA, Antisense
  • Transcription Factors
  • Tubulin
  • DNA
  • Nucleoside-Diphosphate Kinase
  • Monomeric GTP-Binding Proteins