pubmed-article:9212746 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C0225336 | lld:lifeskim |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C0063695 | lld:lifeskim |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C1749467 | lld:lifeskim |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C0041904 | lld:lifeskim |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C0162493 | lld:lifeskim |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C0175630 | lld:lifeskim |
pubmed-article:9212746 | lifeskim:mentions | umls-concept:C0443199 | lld:lifeskim |
pubmed-article:9212746 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:9212746 | pubmed:dateCreated | 1997-7-31 | lld:pubmed |
pubmed-article:9212746 | pubmed:abstractText | Although circulating levels of soluble intercellular adhesion molecule-1 (sICAM-1) are frequently used as an indicator of the severity of different immune, inflammatory, or neoplastic diseases, little is known about the factors that govern plasma sICAM-1 concentration and its relationship to the membranous form of ICAM-1 (mICAM-1) expressed on vascular endothelial cells. Plasma sICAM-1 concentration (measured by enzyme-linked immunosorbent assay) and mICAM-1 expression (measured using the dual radiolabeled monoclonal antibody technique) in different vascular beds (eg, lung, small intestine, and spleen) were monitored in wild-type (C57BL) and ICAM-1-deficient mice, before and after administration of tumor necrosis factor (TNF)-alpha. In wild-type mice, TNF-alpha elicited time-dependent increases in lung and intestine mICAM-1 (plateau achieved at 12 hours), with a corresponding increase in plasma sICAM-1 (peaked at 5 hours and then declined). The initial increases in mICAM-1 and pulmonary leukocyte sequestration (measured as lung myeloperoxidase activity) induced by TNF-alpha preceded any detectable elevation in sICAM-1. In ICAM-1-deficient mice, plasma sICAM-1 was reduced by approximately 70%, with > 95% reductions of mICAM-1 in lung and intestine, and > 75% reduction in splenic accumulation of anti-ICAM-1 antibody. Although TNF-alpha doubled plasma sICAM-1 in ICAM-1-deficient mice, mICAM-1 was unaffected in all tissues. Either splenectomy or pretreatment with cycloheximide resulted in an attenuated TNF-induced increase in sICAM-1, without affecting mICAM-1 expression. These findings indicate that plasma sICAM-1 concentration does not accurately reflect the level of ICAM-1 expression on endothelial cells in different vascular beds. | lld:pubmed |
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pubmed-article:9212746 | pubmed:language | eng | lld:pubmed |
pubmed-article:9212746 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9212746 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:9212746 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9212746 | pubmed:month | Jul | lld:pubmed |
pubmed-article:9212746 | pubmed:issn | 0002-9440 | lld:pubmed |
pubmed-article:9212746 | pubmed:author | pubmed-author:GerritsenM... | lld:pubmed |
pubmed-article:9212746 | pubmed:author | pubmed-author:GrangerD NDN | lld:pubmed |
pubmed-article:9212746 | pubmed:author | pubmed-author:AndersonD CDC | lld:pubmed |
pubmed-article:9212746 | pubmed:author | pubmed-author:KomatsuSS | lld:pubmed |
pubmed-article:9212746 | pubmed:author | pubmed-author:FloreaAA | lld:pubmed |
pubmed-article:9212746 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9212746 | pubmed:volume | 151 | lld:pubmed |
pubmed-article:9212746 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9212746 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9212746 | pubmed:pagination | 205-14 | lld:pubmed |
pubmed-article:9212746 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:9212746 | pubmed:year | 1997 | lld:pubmed |
pubmed-article:9212746 | pubmed:articleTitle | Differential up-regulation of circulating soluble and endothelial cell intercellular adhesion molecule-1 in mice. | lld:pubmed |
pubmed-article:9212746 | pubmed:affiliation | Department of Molecular and Cellular Physiology, Louisiana State University Medical Center, Shreveport 71130-3932, USA. | lld:pubmed |
pubmed-article:9212746 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:9212746 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:9212746 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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