Sustained tyrosine phosphorylation of p140trkA in PC12h-R cells responding rapidly to NGF

Brain Res. 1994 Oct 24;661(1-2):137-46. doi: 10.1016/0006-8993(94)91190-8.

Abstract

The PC12h cell, a subclone of PC12 cells, has considerable activities of tyrosine hydroxylase (TH) and choline acetyltransferase (ChAT) and shows an NGF-induced increase in both enzyme activities. The TH activity and its inducibility by NGF in PC12h cells were stably maintained in the passage of > 200 generations whereas the ChAT activity was not. We isolated a new cell line, PC12h-R (originally clone 8), from a long-term culture of PC12h cells. PC12h-R cells still showed the considerable TH activity, but not the ChAT activity, and maintained the inducibility of TH activity by NGF. Thus, the responses of PC12h-R cells to NGF were similar to those of chromaffin cells and sympathetic neurons. PC12h-R cells were found to extend neurites and differentiate into sympathetic neuron-like cells in response to NGF much more rapidly than PC12h cells. In addition, PC12h-R cells showed sustained NGF-induced tyrosine phosphorylation of p140trkA and several cellular proteins, including 42-, 44- and 54-kDa proteins, in comparison with PC12h cells. We suggest that the NGF-induced sustained tyrosine phosphorylation signal in PC12h-R cells may be correlated closely with their rapid NGF-induced differentiation into neuron-like cells.

Publication types

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

MeSH terms

  • Animals
  • Choline O-Acetyltransferase / metabolism*
  • Clone Cells
  • Electrophoresis, Polyacrylamide Gel
  • Immunoblotting
  • Kinetics
  • Molecular Weight
  • Nerve Growth Factors / pharmacology*
  • Neurites / drug effects
  • Neurites / physiology
  • PC12 Cells
  • Phosphoproteins / isolation & purification
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Phosphotyrosine
  • Proto-Oncogene Proteins / metabolism*
  • Rats
  • Receptor Protein-Tyrosine Kinases / metabolism*
  • Receptor, trkA
  • Receptors, Nerve Growth Factor / metabolism*
  • Tyrosine / analogs & derivatives*
  • Tyrosine / metabolism
  • Tyrosine 3-Monooxygenase / metabolism*

Substances

  • Nerve Growth Factors
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • Receptors, Nerve Growth Factor
  • Phosphotyrosine
  • Tyrosine
  • Tyrosine 3-Monooxygenase
  • Choline O-Acetyltransferase
  • Receptor Protein-Tyrosine Kinases
  • Receptor, trkA