Intrastriatal transforming growth factor alpha delivery to a model of Parkinson's disease induces proliferation and migration of endogenous adult neural progenitor cells without differentiation into dopaminergic neurons

J Neurosci. 2004 Oct 13;24(41):8924-31. doi: 10.1523/JNEUROSCI.2344-04.2004.

Abstract

We examined the cell proliferative, neurogenic, and behavioral effects of transforming growth factor alpha (TGFalpha) in a 6-OHDA Parkinson's disease model when compared with naive rats. Intrastriatal TGFalpha infusion induced significant proliferation, hyperplastic nodules, and substantial migratory waves of nestin-positive progenitor cells from the adult subventricular zone (SVZ) of dopamine-denervated rats. Interestingly, SVZ cells in naive rats displayed proliferation but minimal migration in response to the TGFalpha infusion. The cells in the expanded SVZ accumulated cytoplasmic beta-catenin, indicating activation of classical Wnt signaling. However, no evidence of any neuronal differentiation was found of these recruited progenitor cells anywhere examined in the brain. Consequently, no evidence of dopaminergic (DA) neurogenesis was found in the striatum or substantia nigra in any experimental group, and amphetamine-induced behavioral rotations did not improve. In summary, the cells in the TGFalpha-induced migratory cellular wave remain undifferentiated and do not differentiate into midbrain-like DA neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Bromodeoxyuridine
  • Cell Movement / drug effects*
  • Cell Proliferation / drug effects
  • Corpus Striatum / drug effects*
  • Corpus Striatum / pathology
  • Cytoskeletal Proteins / metabolism
  • Disease Models, Animal
  • Dopamine / metabolism
  • Drug Administration Routes
  • Intermediate Filament Proteins / biosynthesis
  • Lateral Ventricles / cytology
  • Lateral Ventricles / drug effects
  • Lateral Ventricles / metabolism
  • Male
  • Nerve Tissue Proteins / biosynthesis
  • Nestin
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / pathology
  • Oxidopamine
  • Parkinsonian Disorders / chemically induced
  • Parkinsonian Disorders / drug therapy*
  • Parkinsonian Disorders / pathology
  • Rats
  • Rats, Sprague-Dawley
  • Stem Cells / drug effects*
  • Stem Cells / pathology
  • Trans-Activators / metabolism
  • Transforming Growth Factor alpha / administration & dosage*
  • Tyrosine 3-Monooxygenase / biosynthesis
  • beta Catenin

Substances

  • Ctnnb1 protein, rat
  • Cytoskeletal Proteins
  • Intermediate Filament Proteins
  • Nerve Tissue Proteins
  • Nes protein, rat
  • Nestin
  • Trans-Activators
  • Transforming Growth Factor alpha
  • beta Catenin
  • Oxidopamine
  • Tyrosine 3-Monooxygenase
  • Bromodeoxyuridine
  • Dopamine