Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2009-4-24
pubmed:abstractText
Microparticles are small vesicles playing a crucial role in cell communication by promoting prothrombotic and proinflammatory responses. However, the molecular mechanisms underlying their release are still elusive. We previously established that thrombin promoted the generation of endothelial microparticles (EMPs). In the present study, gene profiling identified TRAIL/Apo2L, a cytokine belonging to the tumor necrosis factor-alpha superfamily, as a target of thrombin. Thrombin increased the expression of cell-associated and soluble forms of TRAIL (sTRAIL) in HMEC-1 cells and human umbilical vein endothelial cells (HUVECs). Blocking TRAIL by specific antibodies or by small interfering RNA reduced both the number and the procoagulant activity of EMPs released by thrombin. Consistent with an involvement of sTRAIL in thrombin-induced EMP release, we showed that (1) exogenously added sTRAIL generated procoagulant EMPs; (2) supernatants from thrombin-stimulated endothelial cells induced EMP release by HMEC-1 cells and HUVECs, whereas those recovered from TRAIL knockdown endothelial cells displayed no effect. TRAIL/TRAIL-R2 complex mediated EMP release by initiating the recruitment of adaptor proteins and the activation of nuclear factor kappaB. Moreover, sTRAIL modulated intercellular adhesion molecule-1 and interleukin-8 expression induced by thrombin by a downstream pathway involving nuclear factor kappaB activation. Our data reveal a novel mechanism controlling EMP release and identify TRAIL as a key partner in the pathway linking coagulation and inflammation elicited by thrombin.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Culture Media, Conditioned, http://linkedlifedata.com/resource/pubmed/chemical/IL8 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Adhesion Molecule-1, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-8, http://linkedlifedata.com/resource/pubmed/chemical/RELA protein, human, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, TNF-Related..., http://linkedlifedata.com/resource/pubmed/chemical/TNF-Related Apoptosis-Inducing..., http://linkedlifedata.com/resource/pubmed/chemical/TNFRSF10B protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TNFSF10 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Thrombin, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor RelA
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1524-4571
pubmed:author
pubmed:issnType
Electronic
pubmed:day
24
pubmed:volume
104
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
943-51
pubmed:meshHeading
pubmed-meshheading:19265041-Blood Coagulation, pubmed-meshheading:19265041-Cell-Derived Microparticles, pubmed-meshheading:19265041-Cells, Cultured, pubmed-meshheading:19265041-Culture Media, Conditioned, pubmed-meshheading:19265041-Endothelial Cells, pubmed-meshheading:19265041-Gene Expression Profiling, pubmed-meshheading:19265041-Humans, pubmed-meshheading:19265041-Inflammation, pubmed-meshheading:19265041-Intercellular Adhesion Molecule-1, pubmed-meshheading:19265041-Interleukin-8, pubmed-meshheading:19265041-RNA, Small Interfering, pubmed-meshheading:19265041-RNA Interference, pubmed-meshheading:19265041-Receptors, TNF-Related Apoptosis-Inducing Ligand, pubmed-meshheading:19265041-Signal Transduction, pubmed-meshheading:19265041-TNF-Related Apoptosis-Inducing Ligand, pubmed-meshheading:19265041-Thrombin, pubmed-meshheading:19265041-Thrombosis, pubmed-meshheading:19265041-Time Factors, pubmed-meshheading:19265041-Transcription Factor RelA, pubmed-meshheading:19265041-Transfection, pubmed-meshheading:19265041-Up-Regulation
pubmed:year
2009
pubmed:articleTitle
TRAIL/Apo2L mediates the release of procoagulant endothelial microparticles induced by thrombin in vitro: a potential mechanism linking inflammation and coagulation.
pubmed:affiliation
Faculte de Pharmacie, Institut National de la Santé et de la Recherche Médicale UMR608, Physiopathologie de l'Endothelium, Universite Mediterranee, Marseille, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't