pubmed-article:12811582 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0027651 | lld:lifeskim |
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pubmed-article:12811582 | lifeskim:mentions | umls-concept:C1510411 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0018270 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0205359 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C2246239 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0443211 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C1553412 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C1548328 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:12811582 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:12811582 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:12811582 | pubmed:dateCreated | 2003-8-11 | lld:pubmed |
pubmed-article:12811582 | pubmed:abstractText | Transplantable tumor (KE) and clone cell (KE-F11) lines were established from a spontaneous malignant schwannoma found in an aged F344 rat. The primary tumor and KE tumors consisted of oval or spindle cells arranged in ill-defined bundles. Cultured KE-F11 cells exhibited polygonal or spindle configurations. Immunohistochemically, neoplastic cells in KE and KE-F11 reacted to vimentin, S-100 protein, neuron-specific enolase, myelin basic protein, and glial fibrillary acidic protein in varying degrees, indicating neurogenic features; occasional cells reacted to alpha-smooth muscle actin. Cells positive for lysosomal enzymes (acid phosphatase and non-specific esterase), and ED1 (rat macrophage specific) were observed in KE-F11, and electron microscopically, cells with many lysosomes were frequently present, indicating expression of macrophage-like phenotypes. Bioassay analysis revealed that KE-F11 cells produced high levels of nerve growth factor. DNA synthesis was inhibited by addition of transforming growth factor-beta1 (TGF-beta1), and Northern blot analysis revealed that expression of c-myc, a cell cycle-related immediate early gene, was depressed by TGF-beta1. Likely, TGF-beta1 is a factor capable of inhibiting cellular growth of Schwann cells. mRNA expression of the low-density lipoprotein receptor-related protein (LRP) was seen in KE-F11 cells by Northern blot analysis, and the level was decreased by lipopolysaccharide (LPS) treatment. LRP may be attributable to regulation of Schwann cell functions. KE-F11 cells seeded on laminin-coated dishes exhibited more extended cytoplasmic projections than on collagen type I-coated dishes. The present study provides evidence that biological properties of malignant schwannoma-derived cells might be affected by exogenous factors such as TGF-beta1, LPS and laminin. These tumor lines may be useful for studies on pathobiological characteristics of Schwann cells. | lld:pubmed |
pubmed-article:12811582 | pubmed:language | eng | lld:pubmed |
pubmed-article:12811582 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12811582 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12811582 | pubmed:month | Sep | lld:pubmed |
pubmed-article:12811582 | pubmed:issn | 0001-6322 | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:TsukamotoYY | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:SakumaSS | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:YasuiHH | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:LaMarreJJ | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:YamateJJ | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:KuwamuraMM | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:ALIXDD | lld:pubmed |
pubmed-article:12811582 | pubmed:author | pubmed-author:KumagaiDD | lld:pubmed |
pubmed-article:12811582 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12811582 | pubmed:volume | 106 | lld:pubmed |
pubmed-article:12811582 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12811582 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12811582 | pubmed:pagination | 221-33 | lld:pubmed |
pubmed-article:12811582 | pubmed:dateRevised | 2007-11-9 | lld:pubmed |
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pubmed-article:12811582 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:12811582 | pubmed:articleTitle | Characterization of newly established tumor lines from a spontaneous malignant schwannoma in F344 rats: nerve growth factor production, growth inhibition by transforming growth factor-beta1, and macrophage-like phenotype expression. | lld:pubmed |
pubmed-article:12811582 | pubmed:affiliation | Laboratories of Veterinary Pathology and Anatomy, Graduate School of Agriculture and Biological Sciences, Osaka Prefecture University, Gakuencho 1-1, Sakai, 599-8531 Osaka, Japan. yamate@vet.osakafu-u.ac.jp | lld:pubmed |
pubmed-article:12811582 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12811582 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:12811582 | pubmed:publicationType | In Vitro | lld:pubmed |
pubmed-article:12811582 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |