Source:http://linkedlifedata.com/resource/pubmed/id/15598879
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007634,
umls-concept:C0038172,
umls-concept:C0040649,
umls-concept:C0086418,
umls-concept:C0205263,
umls-concept:C0458827,
umls-concept:C0521009,
umls-concept:C0871261,
umls-concept:C1521761,
umls-concept:C1548795,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1749467,
umls-concept:C2911692
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pubmed:issue |
3
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pubmed:dateCreated |
2005-2-11
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pubmed:abstractText |
To characterize the response of respiratory epithelium to infection by Staphylococcus aureus (S. aureus), human airway cells were incubated for 1 to 24 h with a supernatant of a S. aureus culture (bacterial supernatant), then profiled with a pangenomic DNA microarray. Because an upregulation of many genes was noticed around 3 h, three independent approaches were then used to characterize the host response to a 3-h contact either with bacterial supernatant or with live bacteria: 1) a DNA microarray containing 4,200 sequence-verified probes, 2) a semiquantitative RT-PCR with a set of 537 pairs of validated primers, or 3) ELISA assay of IL-8, IL-6, TNFalpha, and PGE(2). Among others, Fos, Jun, and EGR-1 were upregulated by the bacterial supernatant and by live bacteria. Increased expression of bhlhb2 and Mig-6, promoter regions which harbor HIF responding elements, was explained by an increased expression of the HIF-1alpha protein. Activation of the inducible form of cyclooxygenase, COX-2, and of the interleukins IL-1, IL-6, and IL-8, as well as of the NF-kappaB pathway, was observed preferentially in cells in contact with bacterial supernatant. Early infection was characterized by an upregulation of anti-apoptotic genes and a downregulation of pro-apoptotic genes. This correlated with a necrotic, rather than apoptotic cell death. Overall, this first global description of an airway epithelial infection by S. aureus demonstrates a larger global response to bacterial supernatant (in term of altered genes and variation factors) than to exponentially growing live bacteria.
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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:month |
Feb
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pubmed:issn |
1531-2267
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
10
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
244-55
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15598879-Cell Culture Techniques,
pubmed-meshheading:15598879-Cell Extracts,
pubmed-meshheading:15598879-Computational Biology,
pubmed-meshheading:15598879-DNA, Complementary,
pubmed-meshheading:15598879-Humans,
pubmed-meshheading:15598879-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:15598879-RNA,
pubmed-meshheading:15598879-Respiratory Mucosa,
pubmed-meshheading:15598879-Staphylococcus aureus,
pubmed-meshheading:15598879-Transcription, Genetic
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pubmed:year |
2005
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pubmed:articleTitle |
Live Staphylococcus aureus and bacterial soluble factors induce different transcriptional responses in human airway cells.
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pubmed:affiliation |
Institut de Pharmacologie Moléculaire et Cellulaire UMR 6097 Centre National de la Recherche Scientifique, Université de Nice-Sophia Antipolis, Valbonne, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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