Regulation of alpha-synuclein by bFGF in cultured ventral midbrain dopaminergic neurons

J Neurochem. 2003 Feb;84(4):803-13. doi: 10.1046/j.1471-4159.2003.01574.x.

Abstract

Alpha-synuclein is a neuronal protein that is implicated in the control of synaptic vesicle function and in Parkinson's disease (PD). Consequently, alterations of alpha-synuclein levels may play a role in neurotransmission and in PD pathogenesis. However, the factors that regulate alpha-synuclein levels are unknown. Growth factors mediate neurotrophic and plasticity effects in CNS neurons, and may play a role in disease states. Here we examine the regulation of alpha-synuclein levels in primary CNS neurons, with particular emphasis on dopaminergic neurons. E18 rat cortical neurons and dopaminergic neurons of E14 rat ventral midbrain showed an induction of alpha-synuclein protein levels with maturation in culture. Application of basic Fibroblast growth factor (bFGF) promoted alpha-synuclein expression selectively within dopaminergic, and not GABAergic or cortical neurons. This induction was blocked by actinomycin D, but not by inhibition of bFGF-induced glial proliferation. alpha-Synuclein levels were not altered by glial-derived neurotrophic factor (GDNF), or by apoptotic stimuli. We conclude that bFGF promotes alpha-synuclein expression in cultured ventral midbrain dopaminergic neurons through a direct transcriptional effect. These results suggest that distinct growth factors may thus mediate plasticity responses or influence disease states in ventral midbrain dopaminergic neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenylpyridinium / toxicity
  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Cell Division / drug effects
  • Cells, Cultured
  • Dopamine / metabolism*
  • Dose-Response Relationship, Drug
  • Fibroblast Growth Factor 2 / pharmacology*
  • Gene Expression Regulation, Developmental
  • Mesencephalon / cytology
  • Mesencephalon / drug effects
  • Mesencephalon / metabolism*
  • Mice
  • Nerve Tissue Proteins / antagonists & inhibitors
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Neuroglia / cytology
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism*
  • RNA, Messenger / metabolism
  • Rats
  • Substantia Nigra / cytology
  • Substantia Nigra / drug effects
  • Substantia Nigra / metabolism
  • Synucleins
  • Transcription, Genetic / physiology
  • Up-Regulation / drug effects
  • alpha-Synuclein
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Antibodies, Monoclonal
  • Nerve Tissue Proteins
  • RNA, Messenger
  • Snca protein, mouse
  • Snca protein, rat
  • Synucleins
  • alpha-Synuclein
  • Fibroblast Growth Factor 2
  • gamma-Aminobutyric Acid
  • 1-Methyl-4-phenylpyridinium
  • Dopamine