Timing and dose regimens of marrow mesenchymal stem cell transplantation affect the outcomes and neuroinflammatory response after ischemic stroke.

Abstract

AIMS:

Intravenous transplantation of bone marrow mesenchymal stem cells (BMSCs) had been documented to improve functional outcome after ischemic stroke. However, the timing and appropriate cell number of transplantation to achieve better outcome after an episode of stroke remain further to be optimized.

METHODS:

To determine the optimal conditions, we transplanted different concentrations of BMSCs at different time points in a rat model of ischemic stroke. Infarction volume and neurological behavioral tests were performed after ischemia.

RESULTS:

We found that transplantation of BMSCs at 3 and 24 h, but not 7 days after focal ischemia, significantly reduced the lesion volume and improved motor deficits. We also found that transplanted cells at 1 × 10(6) to 10(7) , but not at 1 × 10(4) to 10(5) , significantly improved functional outcome after stroke. In addition to inhibiting macrophages/microglia activation in the ischemic brain, BMSC transplantation profoundly reduced infiltration of gamma delta T (γδT) cells, which are detrimental to the ischemic brain, and significantly increased regulatory T cells (Tregs), along with altered Treg-associated cytokines in the ischemic brain.

CONCLUSIONS:

Our data suggest that timing and cell dose of transplantation determine the therapeutic effects after focal ischemia by modulating poststroke neuroinflammation.

• Authors: Liu-Qing Wang, Zhen-Zhen Lin, Hong-Xia Zhang, Bei Shao, Li Xiao, Hui-Gang Jiang, Qi-Chuan Zhuge, Luo-Kun Xie, Brian Wang, Dong-Ming Su, Kun-Lin Jin
• Journal: CNS neuroscience & therapeutics (CNS Neurosci Ther) Vol. 20 Issue 4 Pg. 317-26 (Apr 2014) ISSN: 1755-5949 [Electronic] England
• PMID: 24393245 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
• Copyright: © 2014 John Wiley & Sons Ltd.

Chemical References

• Cytokines

Topics

• Adult
• Animals
• Brain (immunology, pathology, surgery)
• Brain Ischemia (immunology, pathology, surgery)
• Cells, Cultured
• Cytokines (metabolism)
• Disease Models, Animal
• Humans
• Infarction, Middle Cerebral Artery (immunology, pathology, surgery)
• Macrophages (physiology)
• Mesenchymal Stem Cell Transplantation (methods)
• Microglia (physiology)
• Middle Aged
• Rats
• Rats, Sprague-Dawley
• Recovery of Function
• Stroke (immunology, pathology, surgery)
• T-Lymphocytes (physiology)
• Time Factors
• Treatment Outcome