Linked Life Data

11103793

Source:http://linkedlifedata.com/resource/pubmed/id/11103793

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
22
pubmed:dateCreated
2000-12-4
pubmed:abstractText
Expression of inducible nitric oxide synthase (iNOS) has been reported to be involved in certain organs of potential tumorigenesis, including the stomach and colon. The mechanisms for iNOS expression in epithelial cells, however, are not fully understood. In the present study, we investigated the role of macrophages in epithelial iNOS expression by coculturing a stimulated murine macrophage-like cell line, RAW 264.7, with either tumor promoter-sensitive (P+) or promoter-resistant (P-) JB6 murine epidermal cells. After monoculture, treatment of RAW 264.7 cells with IFN-gamma for 24 h generated a large amount of nitrite (NO2-), as reported previously, whereas no increase in NO2- concentration was observed in the IFN-gamma-treated P+ or P-subclones. Interestingly, when IFN-gamma-treated RAW 264.7 cells were cocultured with P+ but not P- cells, we observed a marked increase in NO2- concentration (30.8+/-3.6 microM), which significantly exceeded (P < 0.01) the sum of the concentrations (20.0+/-2.3 microM) added from each cell line monoculture. Western blotting analysis revealed that, after coculture, iNOS protein was up-regulated 55-fold more than the control in JB6 P+ but not in P- cells. IFN-gamma-treated RAW 264.7 cells secreted proinflammatory cytokines, including tumor necrosis factor (TNF)-alpha and interleukin (IL)-1beta. The addition of IFN-gamma-treated RAW 264.7 cell-conditioned media to P+ subclones led to a significant enhancement of NO2- formation that was diminished by the TNF-alpha-specific but not IL-1beta-specific antibody. When combined with IFN-gamma, the recombinant TNF-alpha (1-100 ng/ml) enhanced NO2- formation in JB6 P+ cells, whereas IL-1beta (1-100 ng/ml) did not. These results led us to conclude that IFN-gamma-treated RAW 264.7 cells release TNF-alpha to induce iNOS expression in promoter-sensitive JB6 cells. Thus, we propose the hypothesis that macrophages stimulate neoplastic cells with TNF-alpha via a paracrine loop to induce epithelial iNOS protein expression.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0008-5472
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
60
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6326-31
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:11103793-Animals, pubmed-meshheading:11103793-Carcinogens, pubmed-meshheading:11103793-Cell Communication, pubmed-meshheading:11103793-Cell Line, pubmed-meshheading:11103793-Cell Transformation, Neoplastic, pubmed-meshheading:11103793-Coculture Techniques, pubmed-meshheading:11103793-Culture Media, Conditioned, pubmed-meshheading:11103793-Disease Susceptibility, pubmed-meshheading:11103793-Enzyme Induction, pubmed-meshheading:11103793-Epidermis, pubmed-meshheading:11103793-Gene Expression Regulation, Enzymologic, pubmed-meshheading:11103793-Interferon-gamma, pubmed-meshheading:11103793-Interleukin-1, pubmed-meshheading:11103793-Macrophage Activation, pubmed-meshheading:11103793-Macrophages, pubmed-meshheading:11103793-Mice, pubmed-meshheading:11103793-Nitric Oxide Synthase, pubmed-meshheading:11103793-Nitric Oxide Synthase Type II, pubmed-meshheading:11103793-Nitrites, pubmed-meshheading:11103793-Recombinant Proteins, pubmed-meshheading:11103793-Tumor Necrosis Factor-alpha, pubmed-meshheading:11103793-Up-Regulation
pubmed:year
2000
pubmed:articleTitle
Nitric oxide synthase is induced in tumor promoter-sensitive, but not tumor promoter-resistant, JB6 mouse epidermal cells cocultured with interferon-gamma-stimulated RAW 264.7 cells: the role of tumor necrosis factor-alpha.
pubmed:affiliation
Department of Biotechnological Science, Faculty of Biology-Oriented Science and Technology, Kinki University, Wakayama, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't