Source:http://linkedlifedata.com/resource/pubmed/id/18058311
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-12-6
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pubmed:abstractText |
Acute and chronic exposure to ultraviolet (UV) wavelengths in sunlight can cause adverse reactions in exposed areas of the skin and corneas. UV exposure up-regulates the synthesis of Matrix Metalloproteinses (MMPs) and evidence suggests these enzymes mediate tissue damage. Therefore MMP gene activity can serve as a surrogate marker for bioassays. In this study, we tested the possible utility for this purpose of two stably transfected cell lines (from mouse keratinocytes and rabbit epithelial-like corneal cells) and a transgenic mouse line (line 3445), each harboring a DNA construct containing a bacterial beta-galactosidase (LacZ) reporter gene driven by the rabbit MMP-9 transcriptional promoter. We observed only a weak 2-fold maximal induction of LacZ reporter gene expression in the mouse epidermal cell line after exposure to UV-B irradiation (5, 10, 40 mJ/cm2) and no significant expression of the reporter gene in the rabbit epithelial-like cell line. Similarly negative results were obtained when primary corneal epithelial cells from human and rabbit were exposed to different doses of UV-B irradiation and endogenous MMP-9 gene expression was assayed by zymography and immunoprecipitation analysis. In contrast, when skin from 3-day-old transgenic mouse line 3445 was exposed to UV-B and UV-A, a clear dose-dependent induction of the LacZ reporter gene occurred and the location of gene expression was dependent on the wave-length of irradiation. These results suggest that line 3445 transgenic mice may serve as a useful tool to quantitatively and qualitatively assess the biological effects of UV light and the efficacy of therapeutic agents.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1556-9535
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
383-97
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pubmed:dateRevised |
2009-11-17
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pubmed:meshHeading |
pubmed-meshheading:18058311-Animals,
pubmed-meshheading:18058311-Cell Line,
pubmed-meshheading:18058311-Epithelium, Corneal,
pubmed-meshheading:18058311-Gene Expression Regulation,
pubmed-meshheading:18058311-Genes, Reporter,
pubmed-meshheading:18058311-Lac Operon,
pubmed-meshheading:18058311-Matrix Metalloproteinase 9,
pubmed-meshheading:18058311-Mice,
pubmed-meshheading:18058311-Mice, Transgenic,
pubmed-meshheading:18058311-Promoter Regions, Genetic,
pubmed-meshheading:18058311-Rabbits,
pubmed-meshheading:18058311-Skin,
pubmed-meshheading:18058311-Ultraviolet Rays
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pubmed:year |
2007
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pubmed:articleTitle |
Cell lines and transgenic mice expressing a matrix metalloproteinase-9 promoter-driven reporter gene: potential for assay of ultraviolet light effects and light-inhibiting compounds.
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pubmed:affiliation |
Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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