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MicroRNAs and Immunity in Periodontal Health and Disease

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Journal Int J Oral Sci
Date 2018 Aug 7
PMID 30078842
Citations 54
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Abstract

MicroRNAs (miRNAs) are critical regulators of the host immune and inflammatory response against bacterial pathogens. In the present review, we discuss target genes, target gene functions, the potential regulatory role of miRNAs in periodontal tissues, and the potential role of miRNAs as biomarkers and therapeutics. In periodontal disease, miRNAs exert control over all aspects of innate and adaptive immunity, including the functions of neutrophils, macrophages, dendritic cells and T and B cells. Previous human studies have highlighted some key miRNAs that are dysregulated in periodontitis patients. In the present study, we mapped the major miRNAs that were altered in our reproducible periodontitis mouse model relative to control animals. The miRNAs that were upregulated as a result of periodontal disease in both human and mouse studies included miR-15a, miR-29b, miR-125a, miR-146a, miR-148/148a and miR-223, whereas miR-92 was downregulated. The association of individual miRNAs with unique aspects of periodontal disease and their stability in gingival crevicular fluid underscores their potential as markers for periodontal disease progression or healthy restitution. Moreover, miRNA therapeutics hold great promise for the future of periodontal therapy because of their ability to modulate the immune response to infection when applied in conjunction with synthetic antagomirs and/or relatively straightforward delivery strategies.

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References
1.
Martinez-Nunez R, Louafi F, Sanchez-Elsner T . The interleukin 13 (IL-13) pathway in human macrophages is modulated by microRNA-155 via direct targeting of interleukin 13 receptor alpha1 (IL13Ralpha1). J Biol Chem. 2010; 286(3):1786-94. PMC: 3023473. DOI: 10.1074/jbc.M110.169367. View

2.
Cekici A, Kantarci A, Hasturk H, Van Dyke T . Inflammatory and immune pathways in the pathogenesis of periodontal disease. Periodontol 2000. 2013; 64(1):57-80. PMC: 4500791. DOI: 10.1111/prd.12002. View

3.
Zhang Y, Ma C, Ni L, Zhang C, Wu X, Kumaraguru U . Cross-talk between programmed death-1 and suppressor of cytokine signaling-1 in inhibition of IL-12 production by monocytes/macrophages in hepatitis C virus infection. J Immunol. 2011; 186(5):3093-103. DOI: 10.4049/jimmunol.1002006. View

4.
Fordham J, Naqvi A, Nares S . Regulation of miR-24, miR-30b, and miR-142-3p during macrophage and dendritic cell differentiation potentiates innate immunity. J Leukoc Biol. 2015; 98(2):195-207. PMC: 4501676. DOI: 10.1189/jlb.1A1014-519RR. View

5.
Buchmann K . Evolution of Innate Immunity: Clues from Invertebrates via Fish to Mammals. Front Immunol. 2014; 5:459. PMC: 4172062. DOI: 10.3389/fimmu.2014.00459. View