Cografting of carotid body cells improves the long-term survival, fiber outgrowth and functional effects of grafted dopaminergic neurons

Regen Med. 2012 May;7(3):309-22. doi: 10.2217/rme.12.22.

Abstract

Aims: A major limiting factor for cell therapy in Parkinson's disease is that the survival of grafted dopaminergic neurons is very poor, which may be improved by administration of GDNF, for which the carotid body is a good source.

Materials & methods: Rats with total unilateral dopaminergic denervation were grafted with a cell suspension of rat dopaminergic neuroblasts with or without cell aggregates from the rat carotid body. At 1, 2 and 3 months after grafting, the rats were tested in the cylinder and the rotometer and killed 4 months after grafting.

Results: We observed that the survival of dopaminergic neurons and graft-derived dopaminergic innervation were higher in rats that received mixed grafts. Both grafted groups showed complete recovery in the amphetamine-induced rotation test. However, rats with cografts performed significantly better in the cylinder test.

Conclusion: Cografting of carotid body cells may constitute a useful strategy for cell therapy in Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphetamine
  • Animals
  • Carotid Body / cytology*
  • Carotid Body / transplantation*
  • Cell Aggregation
  • Cell Survival
  • Dopaminergic Neurons / cytology
  • Dopaminergic Neurons / physiology*
  • Dopaminergic Neurons / transplantation*
  • Female
  • Glial Cell Line-Derived Neurotrophic Factor / metabolism
  • Mesencephalon / cytology
  • Mesencephalon / transplantation
  • Motor Activity / physiology
  • Neostriatum / cytology
  • Neostriatum / transplantation
  • Nerve Fibers / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Reproducibility of Results
  • Rotation
  • Substantia Nigra / cytology
  • Time Factors
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Glial Cell Line-Derived Neurotrophic Factor
  • Amphetamine
  • Tyrosine 3-Monooxygenase