Source:http://linkedlifedata.com/resource/pubmed/id/12669881
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-4-2
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pubmed:abstractText |
The increased release of prostaglandins (PG) within pulpal tissues is considered to play a pathogenic role during pulpal disease progression. The rate-limiting step in the formation of PG from arachidonic acid is catalyzed by cyclooxygenase (COX). COX-2 is an inducible enzyme believed to be responsible for PG synthesis at site of inflammation. The effect of proinflammatory cytokines on human pulp cells with special reference to COX-2 expression has not been reported earlier. The aim of the present study was to investigate the effects of interleukin (IL)-1alpha and tumor necrosis factor-alpha (TNF-alpha) on the expression of COX-2 mRNA gene and protein in cultured human pulp cells. Investigations of the time dependence of COX-2 mRNA expression in proinflammatory cytokines-treated human pulp cells revealed a rapid accumulation of the transcript, a significant signal first detectable 1 h after exposure. In addition, both IL-1alpha and TNF-alpha up-regulated COX-2 protein expression by human pulp cells. The kinetics of this response showed that COX-2 was detectable in cell lysates as early as 2 h post proinflammatory cytokines challenge and remained elevated throughout the 24-h incubation period. This suggests that one of the pathogenic mechanisms of pulpal inflammation in vivo may be the synthesis of COX-2 by resident cells in response to a proinflammatory cytokines challenge. COX-2 may play an important role in the regulation of prostanoid formation in the pathogenesis of pulpal inflammation. Taken together, we propose that the use of selective COX-2 inhibitors might provide a valuable tool in the control of pulpal inflammation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
D
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Inflammation Mediators,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PTGS2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Peroxidases,
http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandin-Endoperoxide Synthases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0099-2399
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
201-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12669881-Cell Culture Techniques,
pubmed-meshheading:12669881-Cyclooxygenase 2,
pubmed-meshheading:12669881-Dental Pulp,
pubmed-meshheading:12669881-Enzyme Induction,
pubmed-meshheading:12669881-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:12669881-Humans,
pubmed-meshheading:12669881-Inflammation Mediators,
pubmed-meshheading:12669881-Interleukin-1,
pubmed-meshheading:12669881-Isoenzymes,
pubmed-meshheading:12669881-Membrane Proteins,
pubmed-meshheading:12669881-Peroxidases,
pubmed-meshheading:12669881-Prostaglandin-Endoperoxide Synthases,
pubmed-meshheading:12669881-Pulpitis,
pubmed-meshheading:12669881-RNA, Messenger,
pubmed-meshheading:12669881-Time Factors,
pubmed-meshheading:12669881-Transcription, Genetic,
pubmed-meshheading:12669881-Tumor Necrosis Factor-alpha,
pubmed-meshheading:12669881-Up-Regulation
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pubmed:year |
2003
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pubmed:articleTitle |
Proinflammatory cytokines induce cyclooxygenase-2 mRNA and protein expression in human pulp cell cultures.
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pubmed:affiliation |
Institute of Stomatology, Chung Shan Medical University Hospital, Taichung, Taiwan.
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pubmed:publicationType |
Journal Article
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