Source:http://linkedlifedata.com/resource/pubmed/id/15760676
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2005-3-11
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pubmed:abstractText |
We have previously demonstrated that treatment of the human keratinocyte cell line NCTC 2544 with a UVB dose equivalent to 1h exposure (100 mJ/cm2) results in a significant increase of IL-8 production. In this study, we use specific inhibitors to investigate the role of both PKA- and PKC-mediated pathways in the regulation of UVB-induced IL-8 expression in NCTC 2544 cell line. We show here that the treatment of irradiated human keratinocytes with PKA inhibitors [H89 and PKA inhibitor (PKAi)] induced a significant decrease of IL-8 production at both mRNA and protein levels. However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Using PMA (a potent pharmacological activator of PKC) and calphostin C (a specific PKC inhibitor), we demonstrated an up-regulation of IL-8 in NCTC 2544 cells and a down-regulation of the cytokine in UVB-irradiated cells, respectively. We also observed that in our experimental conditions, staurosporine, an inhibitor of both PKC and PMA-stimulated cellular responses, does not involve PKC inhibition in irradiated cells and significantly decreased NF-kappa B activity in response to UVB radiation. Finally, we concluded that a cAMP-independent PKA activation and a PKC-associated pathway are probably involved in the regulation of UVB-induced IL-8 synthesis in human keratinocytes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cholera Toxin,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP-Dependent Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-8,
http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Staurosporine
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1043-4666
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
7
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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 |
197-207
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15760676-Cell Line,
pubmed-meshheading:15760676-Cholera Toxin,
pubmed-meshheading:15760676-Cyclic AMP,
pubmed-meshheading:15760676-Cyclic AMP-Dependent Protein Kinases,
pubmed-meshheading:15760676-Dinoprostone,
pubmed-meshheading:15760676-Gene Expression Regulation,
pubmed-meshheading:15760676-Humans,
pubmed-meshheading:15760676-Interleukin-8,
pubmed-meshheading:15760676-Keratinocytes,
pubmed-meshheading:15760676-NF-kappa B,
pubmed-meshheading:15760676-Protein Kinase C,
pubmed-meshheading:15760676-Protein Kinase Inhibitors,
pubmed-meshheading:15760676-Signal Transduction,
pubmed-meshheading:15760676-Staurosporine,
pubmed-meshheading:15760676-Ultraviolet Rays
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pubmed:year |
2005
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pubmed:articleTitle |
Contribution of protein kinase A and protein kinase C pathways in ultraviolet B-induced IL-8 expression by human keratinocytes.
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pubmed:affiliation |
Laboratoire d'Immunologie, Virologie et Bactériologie, UFR de Pharmacie, EA3796, IFR 53, 1 avenue du Maréchal Juin, 51100 Reims, France.
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pubmed:publicationType |
Journal Article
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