| Literature DB >> 22661094 |
James R Sissons1, Jacques J Peschon, Frank Schmitz, Rosa Suen, Mark Gilchrist, Alan Aderem.
Abstract
Cellular fusion of macrophages into multinucleated giant cells is a distinguishing feature of the granulomatous response to inflammation, infection, and foreign bodies (Kawai and Akira. 2011. Immunity 34: 637-650). We observed a marked increase in fusion of macrophages genetically deficient in Dicer, an enzyme required for canonical microRNA (miRNA) biogenesis. Gene expression profiling of miRNA-deficient macrophages revealed an upregulation of the IL-4-responsive fusion protein Tm7sf4, and analyses identified miR-7a-1 as a negative regulator of macrophage fusion, functioning by directly targeting Tm7sf4 mRNA. miR-7a-1 is itself an IL-4-responsive gene in macrophages, suggesting feedback control of cellular fusion. Collectively, these data indicate that miR-7a-1 functions to regulate IL-4-directed multinucleated giant cell formation.Entities:
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Year: 2012 PMID: 22661094 PMCID: PMC3381877 DOI: 10.4049/jimmunol.1102477
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422