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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1992-9-24
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pubmed:abstractText |
During liver fibrogenesis, fat-storing cells transform into myofibroblast-like cells and produce increasing amounts of extracellular matrix proteins. Because fat-storing cells produce alpha 2-macroglobulin, an important serine protease inhibitor (serpin), we investigated whether fat-storing cells also synthesize C1-esterase inhibitor, another important serpin. C1-esterase inhibitor synthesis was studied in rat fat-storing cells at day 0, 3 and 7 after isolation by biosynthetic labeling, immunoprecipitation and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Messenger RNA was examined by Northern-blot analysis. C1-esterase inhibitor gene expression and synthesis were detectable in freshly isolated fat-storing cells and increased distinctly during the time in culture. The cellular source of C1-esterase inhibitor in fat-storing cell cultures was also identified by in situ hybridization of cells at different times after isolation. By inhibition of the N-glycosylation using tunicamycin, rat C1-esterase inhibitor was identified as a glycoprotein. The time course of C1-esterase inhibitor secretion was determined by pulse-chase experiments. C1-esterase inhibitor synthesis was increased 6-fold to 10-fold by interferon-gamma. Specific messenger RNA levels were also raised distinctly by this cytokine. In contrast, interferon-alpha and dexamethasone did not alter C1-esterase inhibitor gene expression. Because C1-esterase inhibitor synthesis is increased by advancing culture time and by the inflammatory mediator interferon-gamma, we suggest that fat-storing cells may enhance the deposition of extracellular matrix proteins by inhibiting their degradation.
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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 |
Sep
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pubmed:issn |
0270-9139
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
794-802
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:1505923-Animals,
pubmed-meshheading:1505923-Base Sequence,
pubmed-meshheading:1505923-Blotting, Northern,
pubmed-meshheading:1505923-Cells, Cultured,
pubmed-meshheading:1505923-Complement C1 Inactivator Proteins,
pubmed-meshheading:1505923-Dexamethasone,
pubmed-meshheading:1505923-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:1505923-Female,
pubmed-meshheading:1505923-Interferon-gamma,
pubmed-meshheading:1505923-Lipid Metabolism,
pubmed-meshheading:1505923-Liver,
pubmed-meshheading:1505923-Molecular Sequence Data,
pubmed-meshheading:1505923-Nucleic Acid Hybridization,
pubmed-meshheading:1505923-RNA, Messenger,
pubmed-meshheading:1505923-Rats,
pubmed-meshheading:1505923-Rats, Inbred Strains,
pubmed-meshheading:1505923-Up-Regulation
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pubmed:year |
1992
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pubmed:articleTitle |
Fat-storing cells of the rat liver synthesize and secrete C1-esterase inhibitor; modulation by cytokines.
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pubmed:affiliation |
Department of Internal Medicine, University of Mainz, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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