Source:http://linkedlifedata.com/resource/pubmed/id/20956612
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2011-2-1
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pubmed:abstractText |
Mechanisms controlling resolution of acute inflammation are of wide interest. Here, we investigated microRNAs (miRNAs) in self-limited acute inflammatory exudates and their regulation by resolvin D1 (RvD1). Using real-time PCR analysis, we found in resolving exudates that miR-21, miR-146b, miR-208a, miR-203, miR-142, miR-302d, and miR-219 were selectively regulated (P<0.05) in self-limited murine peritonitis. RvD1 (300 ng/mouse or 15 ?g kg(-1)) reduced zymosan-elicited neutrophil infiltration into the peritoneum 25-50% and shortened the resolution interval (R(i)) by ?4 h. In peritonitis at 12 h, RvD1 up-regulated miR-21, miR-146b, and miR-219 and down-regulated miR-208a in vivo. In human macrophages overexpressing recombinant RvD1 receptors ALX/FPR2 or GPR32, these same miRNAs were significantly regulated (P<0.05) by RvD1 at concentrations as low as 10 nM, recapitulating the in vivo circuit. In addition, RvD1-miRNAs identified herein target cytokines and proteins involved in the immune system, e.g., miR-146b targeted NF-?B signaling, and miR-219 targeted 5-lipoxygenase and reduced leukotriene production. RvD1 also reduced nuclear translocation of NF-?B and SMAD and down-regulated phospho-I?B. Taken together, these results indicate that resolvin-regulated specific miRNAs target genes involved in resolution and establish a novel resolution circuit involving RvD1 receptor-dependent regulation of specific miRNAs.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/R01 DE019938-03,
http://linkedlifedata.com/resource/pubmed/grant/R01 GM038765-25,
http://linkedlifedata.com/resource/pubmed/grant/R01DE019938,
http://linkedlifedata.com/resource/pubmed/grant/R01DK074448,
http://linkedlifedata.com/resource/pubmed/grant/R37GM38765
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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/Docosahexaenoic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/MicroRNAs,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Zymosan,
http://linkedlifedata.com/resource/pubmed/chemical/resolvin D1
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1530-6860
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
544-60
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pubmed:dateRevised |
2011-5-12
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pubmed:meshHeading |
pubmed-meshheading:20956612-Acute Disease,
pubmed-meshheading:20956612-Animals,
pubmed-meshheading:20956612-Docosahexaenoic Acids,
pubmed-meshheading:20956612-Gene Expression Regulation,
pubmed-meshheading:20956612-Inflammation,
pubmed-meshheading:20956612-Mice,
pubmed-meshheading:20956612-MicroRNAs,
pubmed-meshheading:20956612-Peritonitis,
pubmed-meshheading:20956612-Polymerase Chain Reaction,
pubmed-meshheading:20956612-Recombinant Proteins,
pubmed-meshheading:20956612-Zymosan
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pubmed:year |
2011
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pubmed:articleTitle |
MicroRNAs in resolution of acute inflammation: identification of novel resolvin D1-miRNA circuits.
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pubmed:affiliation |
Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital and Harvard Medical School, 77 Ave. Louis Pasteur, Harvard Institutes of Medicine 829, Boston, MA 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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