Linked Life Data

12427593

Source:http://linkedlifedata.com/resource/pubmed/id/12427593

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2002-11-12
pubmed:abstractText
Human immunodeficiency virus (HIV)-1 Tat released from HIV-1-infected monocytes is believed to enter other cells via an integrin-facilitated pathway, resulting in altered gene expression. Indeed, exogenous Tat protein can increase cell adhesion molecule gene expression in human endothelial cells. Signaling pathways initiated by Tat in endothelial cells are not known. We evaluated the ability of endogenous tat to stimulate monocyte adhesion via activation of nuclear factor-kappaB (NF-kappaB) within human umbilical vein endothelial cells. Transfection with pcTat, but not control vector DNA, increased NF-kappaB binding activity, NF-kappaB luciferase reporter activity, and monocyte adhesion. pcTat also increased kappaB-dependent HIV-1-LTR-CAT reporter activity 28-fold compared with a 3-fold increase produced by transfection with an equivalent amount of pcTax (from human leukemia virus). The pcTat-induced increase in pNF-kappaB-Luc activity and monocyte adhesion to endothelial cells was blocked by cotransfection with dominant-negative mutant IkappaBalpha and by incubation with 10 mM aspirin. We conclude that monocyte adhesion to human endothelial cells stimulated by pcTat is mediated via an NF-kappaB-dependent mechanism. Furthermore, inhibition studies using aspirin suggest that pcTat-stimulated NF-kappaB activation and monocyte adhesion occur via a redox-sensitive mechanism.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0363-6135
pubmed:author
pubmed:issnType
Print
pubmed:volume
283
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
H2315-21
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:12427593-Antioxidants, pubmed-meshheading:12427593-Aspirin, pubmed-meshheading:12427593-Cell Adhesion, pubmed-meshheading:12427593-Cell Line, pubmed-meshheading:12427593-Cell Nucleus, pubmed-meshheading:12427593-Electrophoretic Mobility Shift Assay, pubmed-meshheading:12427593-Endothelium, Vascular, pubmed-meshheading:12427593-Enzyme Activation, pubmed-meshheading:12427593-Gene Expression, pubmed-meshheading:12427593-Gene Products, tat, pubmed-meshheading:12427593-Genes, Reporter, pubmed-meshheading:12427593-Genetic Vectors, pubmed-meshheading:12427593-HIV-1, pubmed-meshheading:12427593-Humans, pubmed-meshheading:12427593-I-kappa B Proteins, pubmed-meshheading:12427593-Luciferases, pubmed-meshheading:12427593-Monocytes, pubmed-meshheading:12427593-NF-kappa B, pubmed-meshheading:12427593-Oxidation-Reduction, pubmed-meshheading:12427593-Peptides, pubmed-meshheading:12427593-Recombinant Fusion Proteins, pubmed-meshheading:12427593-Transfection, pubmed-meshheading:12427593-U937 Cells, pubmed-meshheading:12427593-tat Gene Products, Human Immunodeficiency Virus
pubmed:year
2002
pubmed:articleTitle
Transfection of human endothelial cells with HIV-1 tat gene activates NF-kappa B and enhances monocyte adhesion.
pubmed:affiliation
Division of Transplant Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee 53226, USA. gmpieper@mcw.edu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't