4.6 Review

Combined cell-based therapy strategies for the treatment of Parkinson's disease: focus on mesenchymal stromal cells

Journal

NEURAL REGENERATION RESEARCH
Volume 18, Issue 3, Pages 478-484

Publisher

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/1673-5374.350193

Keywords

brain repair; cell replacement; co-grafts; dopaminergic neurons; fetal ventral mesencephalic tissue; mesenchymal stem cells; neural grafting; neural transplantation; neuroblasts; neurotrophic factors

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Parkinson's disease is characterized by motor impairments caused by the loss of dopaminergic neurons. Levodopa provides symptomatic improvements but has side effects. Cell-based replacement offers hope for treating Parkinson's disease. Factors like mechanical trauma and neuroinflammation can cause low survival rate of grafted cells. Co-transplanting neurotrophic factor-secreting cells, such as mesenchymal stromal cells, with dopaminergic neurons can increase cell survival and improve graft outcomes.
Parkinson's disease is a neurodegenerative condition characterized by motor impairments caused by the selective loss of dopaminergic neurons in the substantia nigra. Levodopa is an effective and well-tolerated dopamine replacement agent. However, levodopa provides only symptomatic improvements, without affecting the underlying pathology, and is associated with side effects after long-term use. Cell-based replacement is a promising strategy that offers the possibility to replace lost neurons in Parkinson's disease treatment. Clinical studies of transplantation of human fetal ventral mesencephalic tissue have provided evidence that the grafted dopaminergic neurons can reinnervate the striatum, release dopamine, integrate into the host neural circuits, and improve motor functions. One of the limiting factors for cell therapy in Parkinson's disease is the low survival rate of grafted dopaminergic cells. Different factors could cause cell death of dopaminergic neurons after grafting such as mechanical trauma, growth factor deprivation, hypoxia, and neuroinflammation. Neurotrophic factors play an essential role in the survival of grafted cells. However, direct, timely, and controllable delivery of neurotrophic factors into the brain faces important limitations. Different types of cells secrete neurotrophic factors constitutively and co-transplantation of these cells with dopaminergic neurons represents a feasible strategy to increase neuronal survival. In this review, we provide a general overview of the pioneering studies on cell transplantation developed in patients and animal models of Parkinson's disease, with a focus on neurotrophic factor-secreting cells, with a particular interest in mesenchymal stromal cells; that co-implanted with dopaminergic neurons would serve as a strategy to increase cell survival and improve graft outcomes.

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