Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
1997-6-3
pubmed:abstractText
P-selectin (CD62P) is a Ca2+-dependent endogenous lectin that can be expressed by vascular endothelium and platelets. The major ligand for P-selectin on leukocytes is P-selectin glycoprotein ligand-1 (PSGL-1). P-selectin can also bind to carcinoma cells, but the nature of the ligand(s) on these cells is unknown. Here we investigated the P-selectin binding to a breast and a small cell lung carcinoma cell line that are negative for PSGL-1. We report that CD24, a mucin-type glycosylphosphatidylinositol-linked cell surface molecule on human neutrophils, pre B lymphocytes, and many tumors can promote binding to P-selectin. Latex beads coated with purified CD24 from the two carcinoma cell lines but also neutrophils could bind specifically to P-selectin-IgG. The binding was dependent on divalent cations and was abolished by treatment with O-sialoglycoprotein endopeptidase but not endoglycosidase F or sialidase. The beads were stained with a monoclonal antibody (MoAb) to CD57 (HNK-1 carbohydrate epitope) but did not react with MoAbs against the sialylLe(x/a) epitope. The carcinoma cells and CD24-beads derived from these cells could bind to activated platelets or P-selectin transfected Chinese hamster ovary cells (P-CHO) in a P-selectin-dependent manner and this binding was blocked by soluble CD24. Transfection of human adenocarcinoma cells with CD24 enhanced the P-selectin-dependent binding to activated platelets. Treatment of the carcinoma cells or the CD24 transfectant with phosphatidylinositol-specific phospholipase C reduced CD24 expression and P-selectin-IgG binding concomitantly. These results establish a role of CD24 as a novel ligand for P-selectin on tumor cells. The CD24/P-selectin binding pathway could be important in the dissimination of tumor cells by facilitating the interaction with platelets or endothelial cells.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD24, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD57, http://linkedlifedata.com/resource/pubmed/chemical/CD24 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Epitopes, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G, http://linkedlifedata.com/resource/pubmed/chemical/Ligands, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Mucins, http://linkedlifedata.com/resource/pubmed/chemical/P-Selectin, http://linkedlifedata.com/resource/pubmed/chemical/P-selectin ligand protein
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0006-4971
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
89
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3385-95
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9129046-Amino Acid Sequence, pubmed-meshheading:9129046-Animals, pubmed-meshheading:9129046-Antibodies, Monoclonal, pubmed-meshheading:9129046-Antigens, CD, pubmed-meshheading:9129046-Antigens, CD24, pubmed-meshheading:9129046-Antigens, CD57, pubmed-meshheading:9129046-Base Sequence, pubmed-meshheading:9129046-Binding Sites, pubmed-meshheading:9129046-Blood Platelets, pubmed-meshheading:9129046-Breast Neoplasms, pubmed-meshheading:9129046-CHO Cells, pubmed-meshheading:9129046-Cell Adhesion, pubmed-meshheading:9129046-Chromatography, Affinity, pubmed-meshheading:9129046-Cricetinae, pubmed-meshheading:9129046-DNA Primers, pubmed-meshheading:9129046-Epitopes, pubmed-meshheading:9129046-Female, pubmed-meshheading:9129046-Humans, pubmed-meshheading:9129046-Immunoglobulin G, pubmed-meshheading:9129046-Ligands, pubmed-meshheading:9129046-Lung Neoplasms, pubmed-meshheading:9129046-Membrane Glycoproteins, pubmed-meshheading:9129046-Molecular Sequence Data, pubmed-meshheading:9129046-Mucins, pubmed-meshheading:9129046-Neutrophils, pubmed-meshheading:9129046-P-Selectin, pubmed-meshheading:9129046-Platelet Activation, pubmed-meshheading:9129046-Polymerase Chain Reaction, pubmed-meshheading:9129046-Sequence Homology, Amino Acid, pubmed-meshheading:9129046-Tumor Cells, Cultured
pubmed:year
1997
pubmed:articleTitle
CD24, a mucin-type glycoprotein, is a ligand for P-selectin on human tumor cells.
pubmed:affiliation
Tumor Immunology Programme, German Cancer Research Center, Heidelberg.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't