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Research article summary (published 7 Jun 2009):

Modulation of TLR2 protein expression by miR-105 in human oral keratinocytes.

Full Abstract

Mammalian biological processes such as inflammation, involve regulation of hundreds of genes controlling onset and termination. MicroRNAs (miRNAs) can translationally repress target mRNAs and regulate innate immune responses. Our model system comprised primary human keratinocytes, which exhibited robust differences in inflammatory cytokine production (interleukin-6 and tumor necrosis factor-alpha) following specific Toll-like receptor 2 and 4 (TLR-2/TLR-4) agonist challenge. We challenged these primary cells with Porphyromonas gingivalis (a Gram-negative bacterium that triggers TLR-2 and TLR-4) and performed miRNA expression profiling. We identified miRNA (miR)-105 as a modulator of TLR-2 protein translation in human gingival keratinocytes. There was a strong inverse correlation between cells that had high cytokine responses following TLR-2 agonist challenge and miR-105 levels. Knock-in and knock-down of miR-105 confirmed this inverse relationship. In silico analysis predicted that miR-105 had complementarity for TLR-2 mRNA, and the luciferase reporter assay verified this. Further understanding of the role of miRNA in host responses may elucidate disease susceptibility and suggest new anti-inflammatory therapeutics.

 

Author information

Author/s: Benakanakere, Manjunatha R (MR); Li, Qiyan (Q); Eskan, Mehmet A (MA); Singh, Amar V (AV); Zhao, Jiawei (J); Galicia, Johnah C (JC); Stathopoulou, Panagiota (P); Knudsen, Thomas B (TB); Kinane, Denis F (DF);

Affiliation: Center for Oral Health and Systemic Disease, University of Louisville School of Dentistry, Louisville, Kentucky 40202, USA.

Grants: DE017384 (Agency:NIDCR NIH HHS)

Journal and publication information

Publication Type: Journal Article; Research Support, N.I.H., Extramural

Journal: The Journal of biological chemistry (J Biol Chem), published in United States. (Language: eng)

Reference: 2009-Aug; vol 284 (issue 34) : pp 23107-15

Dates: Created 2009/08/17; Completed 2009/10/06; Revised 2009/10/14;

PMID: 19509287, status: MEDLINE (last retrieved date: 10/15/2009)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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Associated Chemicals: Interleukin-12 Subunit p40 (0) ; Interleukin-6 (0) ; MicroRNAs (0) ; Oligonucleotides (0) ; Toll-Like Receptor 2 (0) ; Tumor Necrosis Factor-alpha (0)

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