Source:http://linkedlifedata.com/resource/pubmed/id/15214047
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0010346,
umls-concept:C0017262,
umls-concept:C0021390,
umls-concept:C0021853,
umls-concept:C0023516,
umls-concept:C0033268,
umls-concept:C0040300,
umls-concept:C0079633,
umls-concept:C0185117,
umls-concept:C0282554,
umls-concept:C0333348,
umls-concept:C0527841,
umls-concept:C1332820,
umls-concept:C1366571,
umls-concept:C1705880,
umls-concept:C2911684
|
pubmed:issue |
7
|
pubmed:dateCreated |
2004-6-23
|
pubmed:abstractText |
Crohn's disease (CD) and ulcerative colitis (UC) are inflammatory bowel diseases (IBD) that are characterized by chronic intestinal inflammation and a constant influx of leukocytes mediated by pro-inflammatory cytokines and chemokines. The intestinal expression of the CXCR1-binding chemokines IL-8/CXCL8 and GCP-2/CXCL6 and the participation of immunocompetent cells in IBD were evaluated. IL-8 production by peripheral blood mononuclear cells (PBMC) from IBD patients, stimulated with endotoxin, plant lectin or double-stranded RNA, was significantly lowered in patients with CD, but not in UC patients or healthy subjects. The reduced chemokine production by PBMC from IBD patients was both IL-8 and CD specific, but not inducer dependent. In serum, most chemokines remained undetectable, while the levels of those that were measurable remained unaltered in IBD patients. GCP-2, but not ENA-78/CXCL5, nor IL-8, were highly expressed by endothelial cells in inflamed intestinal tissue of IBD patients. In contrast, stimulated endothelial cell cultures produced more IL-8 than GCP-2. The selective GCP-2 staining of endothelial cells at sites of ulcerations suggests that GCP-2, despite its low production capacity in vitro, plays a role in IBD that is different from that of structurally (ENA-78) and functionally (IL-8) related ELR(+) CXC chemokines. Thus, the chemokine network shows complementarity rather than redundancy.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CXCL6 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CXCL6,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CXC,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-8,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-8A
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0014-2980
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
34
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1992-2000
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:15214047-Chemokine CXCL6,
pubmed-meshheading:15214047-Chemokines, CXC,
pubmed-meshheading:15214047-Crohn Disease,
pubmed-meshheading:15214047-Down-Regulation,
pubmed-meshheading:15214047-Endothelial Cells,
pubmed-meshheading:15214047-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:15214047-Humans,
pubmed-meshheading:15214047-Immunohistochemistry,
pubmed-meshheading:15214047-Inflammation,
pubmed-meshheading:15214047-Intercellular Signaling Peptides and Proteins,
pubmed-meshheading:15214047-Interleukin-8,
pubmed-meshheading:15214047-Intestines,
pubmed-meshheading:15214047-Leukocytes,
pubmed-meshheading:15214047-Receptors, Interleukin-8A
|
pubmed:year |
2004
|
pubmed:articleTitle |
CXCR1-binding chemokines in inflammatory bowel diseases: down-regulated IL-8/CXCL8 production by leukocytes in Crohn's disease and selective GCP-2/CXCL6 expression in inflamed intestinal tissue.
|
pubmed:affiliation |
Laboratory of Molecular Immunology, Rega Institute for Medical Research, University of Leuven, Leuven, Belgium.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|