Adipose-derived stem cells decreased microglia activation and protected dopaminergic loss in rat lipopolysaccharide model

J Cell Physiol. 2019 Aug;234(8):13762-13772. doi: 10.1002/jcp.28055. Epub 2019 Jan 13.

Abstract

Adult stem cell therapy is being used extensively to rejuvenate damaged tissue. One important tissue source to obtain these cells is adipose, which contains cells called adipose-derived stem cells (ADSCs). These cells have a great therapeutic potential not only for their multipotent properties as well as for immunomodulatory effects on the immune system. Parkinson's disease is characterized as neurodegenerative disorder which etiology is undoubtedly related to neuroinflammation process. The properties of ADSCs can be used as a new tool in stem cells therapy to treat neurodegenerative disorders. However, their efficacies are still controversial. Some authors have reported neuroprotection effects, while others did not find differences or stem cells increased the damage. Our previous study showed that ADSCs can survive long time after transplantation, suggesting us some biological effects could need more time to be repaired. In this study, we assessed the neuroprotection 6 months after transplantation. Our results suggest ADSCs can protect the dopaminergic loss after lipopolysaccharide (LPS) injection both reducing the microglia activation and differentiating into dopaminergic cells.

Keywords: Parkinson; adipose tissue stem cells; adult stem cells; engraftment; mesenchymal stem cells; neuroprotection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival
  • Disease Models, Animal
  • Dopaminergic Neurons / pathology*
  • Lipopolysaccharides / toxicity*
  • Male
  • Mesenchymal Stem Cell Transplantation / methods*
  • Mesenchymal Stem Cells
  • Microglia / drug effects
  • Microglia / immunology
  • Microglia / metabolism*
  • Nerve Degeneration / chemically induced
  • Nerve Degeneration / pathology
  • Rats
  • Rats, Wistar
  • Substantia Nigra / pathology*

Substances

  • Lipopolysaccharides