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Bone morphogenetic proteins but not growth differentiation factors induce dopaminergic differentiation in mesencephalic precursors.

Abstract
Bone morphogenetic proteins (BMPs) and growth differentiation factors (GDFs) are potential therapeutic molecules for the treatment of Parkinson's disease (PO). Here we compare the effects of BMP3, 5, 6, and 7 and GDF5 and 6 in a rat mesencephalic cell culture system that reflects the developmental stage of neurons around birth. High concentrations of BMP5, 6, and 7 and GDF5 and 6 induced astroglial cell fate and a depletion of oligodendrocytes. Only BMP5, 6, and 7, however, significantly increased the number of tyrosine hydroxylase (TH)-positive neurons and induced nuclear translocation of the phosphorylated BMP-restricted Smad in a substantial number of TH- and microtubule-associated protein 2(MAP2ab)-positive cells. None of the proteins protected TH-positive cells against 6-hydroxydopamine-induced oxidative stress. BMP3 was without any effect throughout the studies. We conclude that BMP5, 6, and 7 act directly and independently on precursors of the dopaminergic and astroglial lineage and induce their differentiation. In contrast, GDF5 and 6 primarily affect nonneuronal cells in mesencephalic cultures of this stage.
AuthorsA Brederlau, R Faigle, P Kaplan, P Odin, K Funa
JournalMolecular and cellular neurosciences (Mol Cell Neurosci) Vol. 21 Issue 3 Pg. 367-78 (Nov 2002) ISSN: 1044-7431 [Print] United States
PMID12498780 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Bone Morphogenetic Proteins
  • Growth Substances
  • Neuroprotective Agents
  • Oxidopamine
  • Tyrosine 3-Monooxygenase
  • Dopamine
Topics
  • Animals
  • Bone Morphogenetic Proteins (pharmacology, therapeutic use)
  • Brain Tissue Transplantation
  • Cell Differentiation (drug effects, physiology)
  • Cell Survival (drug effects, physiology)
  • Cells, Cultured
  • Dopamine (metabolism)
  • Dose-Response Relationship, Drug
  • Fetus
  • Graft Survival (drug effects, physiology)
  • Growth Substances (pharmacology, therapeutic use)
  • Neurons (cytology, drug effects, metabolism)
  • Neuroprotective Agents (pharmacology)
  • Oligodendroglia (cytology, drug effects, metabolism)
  • Oxidopamine (pharmacology)
  • Parkinson Disease (therapy)
  • Rats
  • Rats, Sprague-Dawley
  • Stem Cells (cytology, drug effects, metabolism)
  • Substantia Nigra (cytology, drug effects, embryology)
  • Tyrosine 3-Monooxygenase (metabolism)

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