GDNF applied to the MPTP-lesioned nigrostriatal system requires TGF-β for its neuroprotective action

Abstract

GDNF is a potent neurotrophic factor for nigrostriatal dopaminergic neurons in vitro and in animal models of Parkinson's disease (PD), but has largely failed when tested in therapeutic applications in human PD. We report here that GDNF requires transforming growth factor-β (TGF-β) to elicit its neurotrophic activity. Lesioning the mouse nigrostriatal system with MPTP significantly upregulates striatal TGF-β2 mRNA levels. As expected, GDNF protects against the destructive effects of MPTP, including losses of TH-ir nigral neurons, striatal dopamine and TH-ir fibers. Application of antibodies neutralizing all three TGF-β isoforms to the MPTP-lesioned striatum abolishes the neurotrophic effect of GDNF. We show that TGF-β antibodies are not toxic and do not interfere with retrograde transport of iodinated GDNF, suggesting that TGF-β antibodies do not impair internalization and retrograde trafficking of GDNF. We conclude that striatal TGF-β may be essential for permitting exogenous GDNF to act as a neuroprotective factor.

Keywords

• Parkinson's disease
• Neurotrophic factors
• Dopaminergic neurons
• Cell death
• Engrailed-1
• Retrograde transport