Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
16
pubmed:dateCreated
1991-9-18
pubmed:abstractText
Adherence of human eosinophils to cytokine-stimulated endothelial cells, which was only partially due to CD18-dependent pathways, was also mediated by binding to endothelial leukocyte adhesion molecule 1 (ELAM-1) and vascular cell adhesion molecule 1 (VCAM-1). Eosinophils bound specifically to both recombinant soluble ELAM-1 and recombinant soluble VCAM-1. Eosinophil binding to recombinant soluble VCAM-1 and to transfected CHO cells expressing VCAM-1 was inhibited with anti-VCAM-1 (4B9) and anti-very late activation antigen 4 (anti-VLA-4; HP1/2 or HP2/1) monoclonal antibodies. Eosinophils, but not neutrophils, expressed VLA-4 detected by cytofluorography. Eosinophil adherence to tumor necrosis factor alpha-stimulated human umbilical vein endothelial cells was partially blocked by monoclonal antibodies against ELAM-1 (BB11) and VCAM-1 (4B9) and against VLA-4 (HP2/1). Thus, while both eosinophils and neutrophils can bind to activated endothelial cells by adherence to ICAM-1 and ELAM-1, only eosinophils expressed VLA-4 and adhered to VCAM-1 on activated endothelial cells. Eosinophil adherence to VCAM-1 might provide a mechanism contributing to the selective recruitment of eosinophils into tissue sites of inflammation.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1689216, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1695647, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1697461, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1697486, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1697696, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1698865, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1702034, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1702804, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1702807, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1704191, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1711067, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1851800, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1967851, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1968426, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-1977836, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2116236, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2188667, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2196321, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2252260, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2428877, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2430809, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2460564, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2543245, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2688898, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2785856, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-2974055, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-3279115, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-3497921, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-3900232, http://linkedlifedata.com/resource/pubmed/commentcorrection/1714604-6644024
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
88
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7430-3
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1991
pubmed:articleTitle
Human eosinophil adherence to vascular endothelium mediated by binding to vascular cell adhesion molecule 1 and endothelial leukocyte adhesion molecule 1.
pubmed:affiliation
Department of Medicine, Charles A. Dana Research Institute, Beth Israel Hospital, Harvard Medical School, Boston, MA 02215.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't