http://www.cnr.it/ontology/cnr/individuo/prodotto/ID37409
Expression of BCL-2 via adeno-associated virus vectors rescues thalamic neurons after visual cortex lesion in the adult rat (Articolo in rivista)
- Type
- Label
- Expression of BCL-2 via adeno-associated virus vectors rescues thalamic neurons after visual cortex lesion in the adult rat (Articolo in rivista) (literal)
- Anno
- 2002-01-01T00:00:00+01:00 (literal)
- Alternative label
Caleo M., Cenni M. C., Costa M., Menna E., Zentilin L., Giadrossi S., Giacca M., Maffei L. (2002)
Expression of BCL-2 via adeno-associated virus vectors rescues thalamic neurons after visual cortex lesion in the adult rat
in European journal of neuroscience (Print)
(literal)
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- Caleo M., Cenni M. C., Costa M., Menna E., Zentilin L., Giadrossi S., Giacca M., Maffei L. (literal)
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- Rivista
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- ISI Web of Science (WOS) (literal)
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- CNR Neuroscienze (literal)
- Titolo
- Expression of BCL-2 via adeno-associated virus vectors rescues thalamic neurons after visual cortex lesion in the adult rat (literal)
- Abstract
- Lesions of the mammalian visual cortex cause the retrograde degeneration
of the thalamic neurons projecting to the damaged cortex. The proto-
oncogene bcl-2 is known to inhibit neuronal apoptosis induced by a variety
of noxious stimuli and preserve the functional integrity of the injured
cells. Here we have tested whether the overexpression of bcl-2 via adeno-
associated virus (AAV) vectors is able to protect the neurons in the
lateral geniculate nucleus after visual cortex ablation in adult rats.
Recombinant AAV vectors encoding Bcl-2 (AAV-Bcl-2) or green fluorescent
protein (AAV-GFP) as a control were stereotaxically injected into the
geniculate. Three weeks after vector injection, the ipsilateral visual
cortex was removed by aspiration, and cell survival was assessed 2 weeks
later. We found that 20% of the geniculate neurons were transduced by the
Bcl-2 vector. These cells were completely protected from death following
cortical ablation. Delivery of AAV-GFP transduced an identical number of
geniculate neurons but had no effect on cell survival after lesion. The
total number of surviving geniculate neurons was found to be significantly
higher in animals injected with AAV-Bcl-2 than in rats injected with AAV-
GFP or in control lesioned rats. These data indicate that Bcl-2 gene
therapy with AAV vectors represents an effective treatment to promote
neuronal survival after central nervous system insults. (literal)
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