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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1994-7-20
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pubmed:abstractText |
Brain tumors induced by transplacental application of ethyl-nitrosourea (ENU) in F344 rats were immunohistochemically demonstrated to consist of undifferentiated cells, astriocyte-like cells, oligodendroglia-like cells, and two distinct types of vimentin-expressing cell groupings termed as perivascular small cell nests (PSCNs) and large cell nests (LCNs). Co-distribution of vimentin and glial fibrillary acidic protein (GFAP) was sparsely observed in the astrocyte-like cells, which suggested an immature glial phenotype. PCSNs contained cells expressing GFAP, neuron-specific enolase (NSE), beta-tubulin isotype III, and low-affinity nerve growth factor receptors (LNGFRs). LCNs contained cells showing a neuronal phenotype with expression of low- and middle-molecular mass neurofilament proteins (NF-L and -M) as well as NSE, beta-tubulin isotype III and LNGFR. Double-labelling immunohistochemistry revealed the NF-L-expression in LNGFR-positive LCN-forming cells. Oligodendroglia-like cells and their intercellular neuropil-like structures expressed beta-tubulin isotype III, synaptophysin and NSE, in addition to the expressions of vimentin and GFAP. Electron microscopically, synapse-like structures were formed between these oligodendroglia-like cells and their dendritic processes. Topographically, bidirectional cell transitions from PSCNs to astrocytes and LCNs were indicated. The present study strongly suggests that so-called ENU-induced "gliomas" originate from pluripotent germinal neuroepithelium. Furthermore, LNGFR expression may be responsible for acquisition of neuronal phenotype in these tumors.
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pubmed:commentsCorrections | |
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:issn |
0001-6322
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
87
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
293-301
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pubmed:dateRevised |
2007-11-9
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pubmed:meshHeading |
pubmed-meshheading:8009961-Animals,
pubmed-meshheading:8009961-Cell Differentiation,
pubmed-meshheading:8009961-Cell Division,
pubmed-meshheading:8009961-Central Nervous System Neoplasms,
pubmed-meshheading:8009961-Epithelium,
pubmed-meshheading:8009961-Ethylnitrosourea,
pubmed-meshheading:8009961-Fetus,
pubmed-meshheading:8009961-Immunohistochemistry,
pubmed-meshheading:8009961-Injections,
pubmed-meshheading:8009961-Microscopy, Electron,
pubmed-meshheading:8009961-Nerve Tissue,
pubmed-meshheading:8009961-Neurofilament Proteins,
pubmed-meshheading:8009961-Neurons,
pubmed-meshheading:8009961-Rats,
pubmed-meshheading:8009961-Rats, Inbred F344
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pubmed:year |
1994
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pubmed:articleTitle |
Evidence for an origin of ethyl-nitrosourea-induced rat central nervous system tumors from pluripotent germinal neuroepithelium.
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pubmed:affiliation |
Division of Pathology, Biological Safety Research Center, National Institute of Health Sciences, Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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