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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003069,
umls-concept:C0004112,
umls-concept:C0026336,
umls-concept:C0027752,
umls-concept:C0027754,
umls-concept:C0030567,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0376604,
umls-concept:C0391871,
umls-concept:C0521428,
umls-concept:C0542341,
umls-concept:C1527362,
umls-concept:C2349975
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pubmed:issue |
1-2
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pubmed:dateCreated |
1995-3-2
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pubmed:abstractText |
Previous studies have demonstrated that astrocytes genetically modified to express recombinant nerve growth factor (NGF) support the survival and neuronal transdifferentiation of intrastriatal adrenal chromaffin cell grafts at 2 weeks post-transplantation [15]. The present study was performed to determine whether these effects would be maintained at longer times post-transplantation and, if so, whether the co-grafts would reduce rotational behavior in the unilateral 6-hydroxydopamine-lesioned rat. In the present study, we have demonstrated that primary type I rat astrocytes infected with a replication-defective retrovirus conferring expression of a mouse beta-NGF cDNA sequence secrete NGF at a rate that is approximately 40-fold higher than that of controls (i.e., 8.0 vs. 0.2 pg NGF/h/10(5) cells, respectively). The genetically modified astrocytes were also found to express recombinant NGF following intrastriatal transplantation, as indicated by a 23% increase in striatal NGF content compared with controls, measured at 4 weeks post-transplantation. When NGF-producing astrocytes and adrenal chromaffin cells were co-grafted into the dopamine-denervated striatum of the unilateral 6-hydroxydopamine-lesioned rat, the chromaffin cells displayed extensive neurite outgrowth and a 5-12-fold increase in survival compared to controls at 10 weeks post-grafting. These effects were paralleled by a 60% reduction of apomorphine-induced rotational behavior, suggesting a partial normalization of striatal function. These results suggest that genetically modified astrocytes promote the prolonged survival and function of adrenal chromaffin cell grafts in a rat model of Parkinson's disease.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0006-8993
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
26
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pubmed:volume |
658
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
219-31
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:7834345-Adrenal Medulla,
pubmed-meshheading:7834345-Animals,
pubmed-meshheading:7834345-Animals, Genetically Modified,
pubmed-meshheading:7834345-Apomorphine,
pubmed-meshheading:7834345-Astrocytes,
pubmed-meshheading:7834345-Cells, Cultured,
pubmed-meshheading:7834345-Disease Models, Animal,
pubmed-meshheading:7834345-Male,
pubmed-meshheading:7834345-Motor Activity,
pubmed-meshheading:7834345-Neostriatum,
pubmed-meshheading:7834345-Nerve Growth Factors,
pubmed-meshheading:7834345-Parkinson Disease,
pubmed-meshheading:7834345-Rats,
pubmed-meshheading:7834345-Recombinant Proteins,
pubmed-meshheading:7834345-Rotation,
pubmed-meshheading:7834345-Transplantation, Heterotopic
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pubmed:year |
1994
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pubmed:articleTitle |
Nerve growth factor released by transgenic astrocytes enhances the function of adrenal chromaffin cell grafts in a rat model of Parkinson's disease.
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pubmed:affiliation |
Department of Neurobiology and Anatomy, University of Rochester School of Medicine, NY 14642.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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