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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1995-4-10
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pubmed:abstractText |
The permeation of macromolecular FITC-labeled dextran (molecular weight 70,000) through bovine aortic endothelial cells (BAEC) monolayer, which were cultured for 5 days with conditioned medium prepared from mouse melanoma B16, was increased. However, when BAEC, which were cultured with normal medium until confluent, were treated with B16 conditioned medium (B16-CM) for 30 min, the permeability did not increase. The B16-CM also increased the permeability of the endothelial monolayers of bovine veins and the human umbilical vein, but did not increase that of the epithelial monolayer. The B16-CM did not alter the distribution or content of F-actin on the BAEC. BAEC cultured in the presence of B16-CM for 5 days were detached from the dish, and then seeded into a chamber at one-fifth of confluent cell density. After 5 days of culture in normal medium, the BAEC were grown to confluence and their permeability was increased. These findings suggest that B16-CM increased the endothelial permeability irreversibly without the decrease of F-actin, and that soluble factor(s) which were secreted from the tumor cells participate in the construction of the hyperpermeable structure of tumor vessels in vivo.
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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 |
Feb
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pubmed:issn |
0304-3835
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
10
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pubmed:volume |
89
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7-14
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:7882304-Actins,
pubmed-meshheading:7882304-Animals,
pubmed-meshheading:7882304-Cattle,
pubmed-meshheading:7882304-Cell Membrane Permeability,
pubmed-meshheading:7882304-Culture Media, Conditioned,
pubmed-meshheading:7882304-Dogs,
pubmed-meshheading:7882304-Endothelium, Vascular,
pubmed-meshheading:7882304-Humans,
pubmed-meshheading:7882304-Liver Neoplasms, Experimental,
pubmed-meshheading:7882304-Macromolecular Substances,
pubmed-meshheading:7882304-Melanoma, Experimental,
pubmed-meshheading:7882304-Mice,
pubmed-meshheading:7882304-Rats,
pubmed-meshheading:7882304-Tumor Cells, Cultured
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pubmed:year |
1995
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pubmed:articleTitle |
Tumor-conditioned medium increases macromolecular permeability of endothelial cell monolayer.
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pubmed:affiliation |
Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Osaka University, Japan.
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pubmed:publicationType |
Journal Article
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