Adipose-derived human mesenchymal stem cells induce long-term neurogenic and anti-inflammatory effects and improve cognitive but not motor performance in a rat model of Parkinson's disease

Regen Med. 2015 May;10(4):431-46. doi: 10.2217/rme.15.17.

Abstract

Background: Mesenchymal stem cells (MSC) are easily harvested, and possess anti-inflammatory and trophic properties. Furthermore, MSC promote neuroprotection and neurogenesis, which could greatly benefit neurodegenerative disorders, such as Parkinson's disease.

Methods: MSC were transplanted one week after 6-hydroxydopamine lesioning and effects were evaluated after 6 months.

Results: MSC localized around the substantia nigra and the arachnoid mater, expressing pericyte and endothelial markers. MSC protected dopamine levels and upregulated peripheral anti-inflammatory cytokines. Furthermore, adipose-derived MSC increased neurogenesis in hippocampal and subventricular regions, and boosted memory functioning.

Conclusion: Considering that hyposmia and loss of memory function are two major nonmotor symptoms in Parkinson's disease, transplants with modulatory effects on the hippocampus and subventricular zone could provide a disease-modifying therapy.

Keywords: Parkinson's disease; adipose-derived mesenchymal stem cells; adult stem cells; neurogenesis; plasticity; regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / cytology*
  • Amphetamine
  • Animals
  • Anti-Inflammatory Agents / metabolism*
  • Cognition*
  • Disease Models, Animal
  • Dopaminergic Neurons / pathology
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Hippocampus / pathology
  • Humans
  • Male
  • Maze Learning
  • Memory, Short-Term
  • Mesenchymal Stem Cell Transplantation
  • Mesenchymal Stem Cells / cytology*
  • Motor Activity*
  • Nerve Degeneration / pathology
  • Neurogenesis*
  • Parkinson Disease / pathology
  • Parkinson Disease / physiopathology*
  • Parkinson Disease / therapy*
  • Rats, Wistar
  • Rotation
  • Substantia Nigra / pathology
  • Time Factors
  • Tyrosine 3-Monooxygenase / metabolism
  • Young Adult

Substances

  • Anti-Inflammatory Agents
  • Amphetamine
  • Tyrosine 3-Monooxygenase