Reporter gene-expressing bone marrow-derived stromal cells are immune-tolerated following implantation in the central nervous system of syngeneic immunocompetent mice
2009

Bone Marrow-Derived Cells are Accepted in the Brain of Mice

Sample size: 90 publication 10 minutes Evidence: moderate

Author Information

Author(s): Irene Bergwerf, Nathalie De Vocht, Bart Tambuyzer, Jacob Verschueren, Kristien Reekmans, Jasmijn Daans, Abdelilah Ibrahimi, Viggo Van Tendeloo, Shyama Chatterjee, Herman Goossens, Philippe G. Jorens, Veerle Baekelandt, Dirk Ysebaert, Eric Van Marck, Zwi N. Berneman, Annemie Van Der Linden, Peter Ponsaerts

Primary Institution: University of Antwerp

Hypothesis

Can genetically modified bone marrow-derived stromal cells survive and be tolerated in the central nervous system of immunocompetent mice?

Conclusion

The study shows that reporter gene-modified bone marrow-derived stromal cells are immune-tolerated when implanted in the central nervous system of syngeneic immunocompetent mice.

Supporting Evidence

  • BMSC-Luc and BMSC-Luc/eGFP/Pac showed high engraftment capacity in the CNS.
  • Real-time bioluminescence imaging confirmed the survival of implanted cells.
  • Histological analysis indicated the presence of BMSC at the implantation site.

Takeaway

Scientists found that special cells from bone marrow can be put into the brain of mice without being rejected by the immune system.

Methodology

The study involved cell implantation experiments in the CNS of immunocompetent mice using genetically modified bone marrow-derived stromal cells, followed by bioluminescence imaging and histological analysis.

Potential Biases

Potential bias in the interpretation of immune responses due to the use of specific mouse strains.

Limitations

The study primarily focused on syngeneic models, which may not fully represent allogeneic transplant scenarios.

Participant Demographics

Male ROSA26-L-S-L-Luciferase transgenic mice were used for the experiments.

Statistical Information

P-Value

<0.01

Statistical Significance

p<0.01

Digital Object Identifier (DOI)

10.1186/1472-6750-9-1

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