Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
14
pubmed:dateCreated
2011-6-24
pubmed:abstractText
The receptor (CXCR4) for the stromal-derived factor-1 (SDF1) and the urokinase-receptor (uPAR) are up-regulated in various tumors. We show that CXCR4-transfected cells migrate toward SDF1 on collagen (CG) and do not on vitronectin (VN). Co-expression of cell-surface uPAR, which is a VN receptor, impairs SDF1-induced migration on CG and allows migration on VN. Blocking fMLP receptors (fMLP-R), alpha-v integrins or the uPAR region capable to interact with fMLP-Rs, impairs migration of uPAR/CXCR4-transfected cells on VN and restores their migration on CG. uPAR co-expression also reduces the adherence of CXCR4-expressing cells to various components of the extracellular matrix (ECM) and influences the partitioning of beta1 and alpha-v integrins to membrane lipid-rafts, affecting ECM-dependent signaling. uPAR interference in CXCR4 activity has been confirmed in cells from prostate carcinoma. Our results demonstrate that uPAR expression regulates the adhesive and migratory ability of CXCR4-expressing cells through a mechanism involving fMLP receptors and alpha-v integrins.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CXCL12, http://linkedlifedata.com/resource/pubmed/chemical/Collagen, http://linkedlifedata.com/resource/pubmed/chemical/FPR3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Integrin alpha5beta1, http://linkedlifedata.com/resource/pubmed/chemical/MAPK1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 1, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 3, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CXCR4, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Formyl Peptide, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Urokinase Plasminogen..., http://linkedlifedata.com/resource/pubmed/chemical/Vitronectin
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1420-9071
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
68
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2453-67
pubmed:meshHeading
pubmed-meshheading:20972812-Blotting, Western, pubmed-meshheading:20972812-Cell Adhesion, pubmed-meshheading:20972812-Cell Line, Tumor, pubmed-meshheading:20972812-Cell Membrane, pubmed-meshheading:20972812-Cell Movement, pubmed-meshheading:20972812-Chemokine CXCL12, pubmed-meshheading:20972812-Collagen, pubmed-meshheading:20972812-Enzyme Activation, pubmed-meshheading:20972812-HEK293 Cells, pubmed-meshheading:20972812-Humans, pubmed-meshheading:20972812-Integrin alpha5beta1, pubmed-meshheading:20972812-Membrane Microdomains, pubmed-meshheading:20972812-Microscopy, Confocal, pubmed-meshheading:20972812-Mitogen-Activated Protein Kinase 1, pubmed-meshheading:20972812-Mitogen-Activated Protein Kinase 3, pubmed-meshheading:20972812-RNA Interference, pubmed-meshheading:20972812-Receptor Cross-Talk, pubmed-meshheading:20972812-Receptors, CXCR4, pubmed-meshheading:20972812-Receptors, Formyl Peptide, pubmed-meshheading:20972812-Receptors, Urokinase Plasminogen Activator, pubmed-meshheading:20972812-Transfection, pubmed-meshheading:20972812-Vitronectin
pubmed:year
2011
pubmed:articleTitle
The cross-talk between the urokinase receptor and fMLP receptors regulates the activity of the CXCR4 chemokine receptor.
pubmed:affiliation
Department of Cellular and Molecular Biology and Pathology, Federico II University, Naples, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't