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  • MicroRNA-155 modulates the interleukin-1 signaling pathway in activated human monocyte-derived dendritic cells.

MicroRNA-155 modulates the interleukin-1 signaling pathway in activated human monocyte-derived dendritic cells.

Proceedings of the National Academy of Sciences of the United States of America (2009-02-06)
Maurizio Ceppi, Patricia M Pereira, Isabelle Dunand-Sauthier, Emmanuèle Barras, Walter Reith, Manuel A Santos, Philippe Pierre
ZUSAMMENFASSUNG

In response to inflammatory stimulation, dendritic cells (DCs) have a remarkable pattern of differentiation (maturation) that exhibits specific mechanisms to control immunity. Here, we show that in response to Lipopolysaccharides (LPS), several microRNAs (miRNAs) are regulated in human monocyte-derived dendritic cells. Among these miRNAs, miR-155 is highly up-regulated during maturation. Using LNA silencing combined to microarray technology, we have identified the Toll-like receptor/interleukin-1 (TLR/IL-1) inflammatory pathway as a general target of miR-155. We further demonstrate that miR-155 directly controls the level of TAB2, an important signal transduction molecule. Our observations suggest, therefore, that in mature human DCs, miR-155 is part of a negative feedback loop, which down-modulates inflammatory cytokine production in response to microbial stimuli.

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Sigma-Aldrich
Lipopolysaccharide aus Escherichia coli O26:B6, γ-irradiated, BioXtra, suitable for cell culture
Sigma-Aldrich
Lipopolysaccharide aus Escherichia coli O26:B6, ≥10,000 EU/mg, purified by phenol extraction
Sigma-Aldrich
Lipopolysaccharide aus Escherichia coli O26:B6, Ready Made solution, 1 mg/mL, 0.2 μm filtered
Sigma-Aldrich
Lipopolysaccharide aus Escherichia coli O26:B6, purified by gel-filtration chromatography
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Lipopolysaccharide aus Escherichia coli O26:B6, purified by trichloroacetic acid extraction