Induction of A9 dopaminergic neurons from neural stem cells improves motor function in an animal model of Parkinsons disease
Neural stem cells (NSCs) are widely endorsed as a cell source for replacement strategies in neurodegenerative disease. However, their usefulness is currently limited by the inability to induce specific neurotransmitter phenotypes in these cells. In order to direct dopaminergic neuronal fate, we overexpressed Pitx3 in NSCs that were then exposed to EII developing ventral mesencephalon (VM) in explant culture. This resulted in a significant potentiation of dopaminergic differentiation of the cells. When transplanted into the 6-hydroxydopamine lesioned Parkinsonian rats, these cografts of VM and Pitx3 overexpressing NSCs resulted in a significant restitution of motor function. In addition, there were greater numbers of Girk2 positive A9 neurons in the periphery of the transplants that were NSC derived. This demonstrates that given the correct signals, NSCs can be induced to become dopaminergic neurons that can differentiate into the correct nigrastriatal phenotype required for the treatment of Parkinsons disease.
Keywords: Parkinson's disease ; neural stem cells ; transcription factors ; dopamine neurons ; Expanded Mesencephalic Precursors ; Fetal Ventral Mesencephalon ; Substantia-Nigra ; In-Vitro ; Pitx3 ; Transplantation ; Mice ; Differentiation ; Proliferation ; Survival
Record created on 2010-11-30, modified on 2016-08-09