Abstract
The present study investigates the survival and
fate of neural stem cells/progenitor cells (NSC/NPCs) homografted
into the hippocampus of rats treated with trimethyltin
(TMT), a potent neurotoxicant considered a useful
tool to obtain a well characterized model of neurodegeneration,
to evaluate their possible role in the reparative
mechanisms that accompany neurodegenerative events.
NSC/NPCs expressing eGFP by lentivirus-mediated
infection were stereotaxically grafted into the hippocampus
of TMT-treated animals and controls. Two weeks after
transplantation surviving NSC/NPCs were detectable in
60% of TMT-treated animals and 30% of controls, while
30 days after transplantation only 40% of TMT-treated
animals showed surviving grafted cells, which were
undetectable in controls. At both times investigated, while
grafted NSC/NPCs differentiated into neurons or astrocytes
could be observed in addition to undifferentiated NSC/
NPCs, we did not find evidence of structural integration of
grafted cells into the main site of hippocampal lesion
leading to appreciable repair.
Lingua originale | English |
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pagine (da-a) | 2054-2061 |
Numero di pagine | 8 |
Rivista | Neurochemical Research |
Volume | 2007 |
Stato di pubblicazione | Pubblicato - 2007 |
Keywords
- hippocampus
- neural stem cells
- neurodegeneration
- transplantation
- trimethyltin