Source:http://linkedlifedata.com/resource/pubmed/id/18664717
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2008-11-17
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pubmed:abstractText |
Ultraviolet (UV) irradiation accelerates formation of ceramide through hydrolysis of sphingomyelin and de novo synthesis. Here, we investigated the effects of ceramide on UV-induced matrix metalloproteinase-1 (MMP-1) expression in human dermal fibroblasts. Our results showed that acidic-sphingomyelinase (aSMase) and MMP-1 mRNA expression were increased by UV irradiation. Treatment of D609 (aSMase inhibitor) decreased the level of basal and UV-induced MMP-1 expression. On the other hand, basal and UV-induced MMP-1 expression was increased through induction of intracellular ceramide by D-MAPP, a ceramidase inhibitor. Our results also showed that MMP-1 protein expression was dose-dependently increased by C(2)-ceramide or SMase treatment. The activation of ceramide pathway by C(2)-ceramide enhanced phosphorylation of signal transducer and activators of transcription-1 (STAT-1), whereas ceramide-induced MMP-1 expression was potently prevented by piceatannol; Janus kinase (JAK1) inhibtor; and WHI-P131, a specific inhibitor of JAK3; but not by AG490, JAK 2 inhbitor, in human dermal fibroblasts. We also found that UV induced the phosphorylation of STAT-1, and UV-induced MMP-1 expression was significantly decreased by JAK1 inhibitor, piceatannol. Overall, we demonstrate that induction of intracellular ceramide by UV may activate MMP-1 gene expression via JAK1/STAT-1 pathway. Therefore, we suggest that targeted modulation of the ceramide signaling pathway may offer a novel therapeutic approach for inhibiting MMP-1 expression, which is a causing gene of skin aging.
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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/Ceramidases,
http://linkedlifedata.com/resource/pubmed/chemical/Ceramides,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/JAK1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Janus Kinase 1,
http://linkedlifedata.com/resource/pubmed/chemical/Janus Kinase 3,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinase 1,
http://linkedlifedata.com/resource/pubmed/chemical/STAT1 Transcription Factor,
http://linkedlifedata.com/resource/pubmed/chemical/STAT1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Sphingomyelin Phosphodiesterase
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-2275
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2571-81
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:18664717-Adult,
pubmed-meshheading:18664717-Cells, Cultured,
pubmed-meshheading:18664717-Ceramidases,
pubmed-meshheading:18664717-Ceramides,
pubmed-meshheading:18664717-Dermis,
pubmed-meshheading:18664717-Enzyme Inhibitors,
pubmed-meshheading:18664717-Fibroblasts,
pubmed-meshheading:18664717-Humans,
pubmed-meshheading:18664717-Janus Kinase 1,
pubmed-meshheading:18664717-Janus Kinase 3,
pubmed-meshheading:18664717-Matrix Metalloproteinase 1,
pubmed-meshheading:18664717-Phosphorylation,
pubmed-meshheading:18664717-STAT1 Transcription Factor,
pubmed-meshheading:18664717-Signal Transduction,
pubmed-meshheading:18664717-Sphingomyelin Phosphodiesterase,
pubmed-meshheading:18664717-Ultraviolet Rays
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pubmed:year |
2008
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pubmed:articleTitle |
Ceramide accelerates ultraviolet-induced MMP-1 expression through JAK1/STAT-1 pathway in cultured human dermal fibroblasts.
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pubmed:affiliation |
Department of Dermatology, Seoul National University College of Medicine, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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