Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
1996-6-27
pubmed:abstractText
Atherogenesis involves cellular immune responses and altered vascular smooth muscle cell (SMC) function. Cytokines such as interleukin (IL)-1 alpha and interferon-gamma (IFN-gamma) may contribute to this process by activating SMC. To determine whether the anti-atherogenic mediator, nitric oxide (.NO), can modulate cytokine-induced SMC activation, we investigated the effects of various .NO-generating compounds on the expression of intercellular and vascular cell adhesion molecules (ICAM-1 and VCAM-1). Induction of ICAM-1 expression by IL-1 alpha and VCAM-1 expression by IFN-gamma was attenuated by .NO donors but not by cGMP analogues. Nuclear run-on assays and transfection studies using various VCAM-1 promoter constructs linked to the chloramphenicol acetyl-transferase reporter gene showed that .NO repressed IFN-gamma-induced VCAM-1 gene transcription, in part, through inhibition of nuclear factor-kappa B (NF-kappa B). Electrophoretic mobility shift assay revealed that SMC possess basal constitutive NF-kappa B activity, which was augmented by treatment with IL-1 alpha. In contrast, IFN-gamma induced and activated interferon regulatory factor (IRF)-1 but had little effect on basal constitutive NF-kappa B activity. .NO donors had no inhibitory effect on IRF-1 activation but did inhibit basal and IL-1 alpha-stimulated NF-kappa B activation. These findings suggest that the induction of ICAM-1 and VCAM-1 expression requires NF-kappa B activation and that .NO attenuates IFN-gamma-induced VCAM-1 expression primarily by inhibiting basal constitutive NF-kappa B activity in SMC.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/3-morpholino-sydnonimine, http://linkedlifedata.com/resource/pubmed/chemical/8-Bromo Cyclic Adenosine..., http://linkedlifedata.com/resource/pubmed/chemical/Chloramphenicol O-Acetyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Adhesion Molecule-1, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/Molsidomine, http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Nitroprusside, http://linkedlifedata.com/resource/pubmed/chemical/Oligodeoxyribonucleotides, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Vascular Cell Adhesion Molecule-1
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
10
pubmed:volume
271
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
11317-24
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:8626684-8-Bromo Cyclic Adenosine Monophosphate, pubmed-meshheading:8626684-Aorta, pubmed-meshheading:8626684-Base Sequence, pubmed-meshheading:8626684-Binding Sites, pubmed-meshheading:8626684-Blotting, Northern, pubmed-meshheading:8626684-Cell Nucleus, pubmed-meshheading:8626684-Chloramphenicol O-Acetyltransferase, pubmed-meshheading:8626684-Humans, pubmed-meshheading:8626684-Intercellular Adhesion Molecule-1, pubmed-meshheading:8626684-Interferon-gamma, pubmed-meshheading:8626684-Interleukin-1, pubmed-meshheading:8626684-Kinetics, pubmed-meshheading:8626684-Molecular Sequence Data, pubmed-meshheading:8626684-Molsidomine, pubmed-meshheading:8626684-Muscle, Smooth, Vascular, pubmed-meshheading:8626684-NF-kappa B, pubmed-meshheading:8626684-Nitric Oxide, pubmed-meshheading:8626684-Nitroprusside, pubmed-meshheading:8626684-Oligodeoxyribonucleotides, pubmed-meshheading:8626684-Promoter Regions, Genetic, pubmed-meshheading:8626684-RNA, Messenger, pubmed-meshheading:8626684-Recombinant Proteins, pubmed-meshheading:8626684-Saphenous Vein, pubmed-meshheading:8626684-Transcription, Genetic, pubmed-meshheading:8626684-Transcription Factors, pubmed-meshheading:8626684-Transfection, pubmed-meshheading:8626684-Tunica Media, pubmed-meshheading:8626684-Vascular Cell Adhesion Molecule-1
pubmed:year
1996
pubmed:articleTitle
Nitric oxide attenuates vascular smooth muscle cell activation by interferon-gamma. The role of constitutive NF-kappa B activity.
pubmed:affiliation
Cardiovascular Division, Brigham & Women's Hospital, Boston, Massachusetts, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't