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Sertoli cells decrease microglial response and increase engraftment of human hNT neurons in the hemiparkinsonian rat
A E Willing1, J J Sudberry, A I Othberg
1Department of Neurosurgery, University of South Florida College of Medicine, Tampa 33612, USA.
Brain Research Bulletin
|June 5, 1999
Summary
Sertoli cells (SCs) demonstrated immunosuppressive abilities in the brain, enhancing neural graft survival and reducing microglial activation in a rat model of Parkinson's disease.
Area of Science:
- Neuroscience
- Immunology
- Cell Biology
Background:
- Sertoli cells (SCs) support germ cell development and have shown immunosuppressive properties in extra-testicular transplants.
- Microglial activation is a key factor in graft rejection within the central nervous system (CNS).
Purpose of the Study:
- To investigate the efficacy of Sertoli cells in mitigating microglial infiltration and activation within neural grafts in a hemiparkinsonian rat model.
- To assess the impact of Sertoli cells on xenograft survival and integration in the brain.
Main Methods:
- Human neuron-like (hNT) cells were implanted into the lesioned striatum of hemiparkinsonian rats, either alone or co-transplanted with rat SCs.
- Immunohistochemistry was employed to evaluate xenograft survival, size, and microglial infiltration/activation three months post-transplantation.
Main Results:
- Co-transplantation with SCs significantly increased the survival and size of the hNT neuron xenografts.
- Fewer microglia were observed in the grafted tissue of animals that received SCs, indicating reduced immune cell infiltration and activation.
- SCs maintained their immunosuppressive function within the brain environment.
Conclusions:
- Sertoli cells possess potent immunosuppressive capabilities that extend to the CNS, protecting neural xenografts from immune attack.
- The localized immunosuppression provided by SCs offers a promising strategy for improving the success of neural transplantation therapies for neurodegenerative diseases.
- SCs represent a potential alternative cell source for enhancing neural graft survival and therapeutic efficacy across species.