Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
17
pubmed:dateCreated
2009-10-14
pubmed:abstractText
microRNA-155 (miR-155) has been implicated as a central regulator of the immune system, but its function during acute inflammatory responses is still poorly understood. Here we show that exposure of cultured macrophages and mice to lipopolysaccharide (LPS) leads to up-regulation of miR-155 and that the transcription factor c/ebp Beta is a direct target of miR-155. Interestingly, expression profiling of LPS-stimulated macrophages combined with overexpression and silencing of miR-155 in murine macrophages and human monocytic cells uncovered marked changes in the expression of granulocyte colony-stimulating factor (G-CSF), a central regulator of granulopoiesis during inflammatory responses. Consistent with these data, we show that silencing of miR-155 in LPS-treated mice by systemically administered LNA-antimiR results in derepression of the c/ebp Beta isoforms and down-regulation of G-CSF expression in mouse splenocytes. Finally, we report for the first time on miR-155 silencing in vivo in a mouse inflammation model, which underscores the potential of miR-155 antagonists in the development of novel therapeutics for treatment of chronic inflammatory diseases.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-10914502, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-11138333, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-11869895, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-11937564, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-1391942, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-14530280, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-15030314, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-15272075, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-16885212, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-16951705, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-17121185, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-17242365, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-1730090, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-17463289, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-17463290, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-17911593, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-17911624, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18055230, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18158304, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18199046, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18299402, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18323801, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18367535, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18368051, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18450484, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18455451, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18515182, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18536574, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-18551128, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-19359473, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-2112087, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-2462934, http://linkedlifedata.com/resource/pubmed/commentcorrection/19596814-8102674
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1362-4962
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5784-92
pubmed:dateRevised
2010-9-27
pubmed:meshHeading
pubmed-meshheading:19596814-Animals, pubmed-meshheading:19596814-CCAAT-Enhancer-Binding Protein-beta, pubmed-meshheading:19596814-Cell Line, pubmed-meshheading:19596814-Down-Regulation, pubmed-meshheading:19596814-Female, pubmed-meshheading:19596814-Gene Expression Regulation, pubmed-meshheading:19596814-Gene Silencing, pubmed-meshheading:19596814-Granulocyte Colony-Stimulating Factor, pubmed-meshheading:19596814-Humans, pubmed-meshheading:19596814-Inflammation, pubmed-meshheading:19596814-Lipopolysaccharides, pubmed-meshheading:19596814-Macrophages, pubmed-meshheading:19596814-Mice, pubmed-meshheading:19596814-Mice, Inbred C57BL, pubmed-meshheading:19596814-MicroRNAs, pubmed-meshheading:19596814-Protein Biosynthesis, pubmed-meshheading:19596814-Protein Isoforms, pubmed-meshheading:19596814-Spleen
pubmed:year
2009
pubmed:articleTitle
Silencing of microRNA-155 in mice during acute inflammatory response leads to derepression of c/ebp Beta and down-regulation of G-CSF.
pubmed:affiliation
Santaris Pharma, Kogle Allé 6, DK-2970 Hørsholm, Denmark.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't