4.4 Article

Initial periodontal treatment affects nucleotide-binding domain leucine-rich repeat-containing protein 3 inflammasome priming in peripheral blood mononuclear cells

Journal

ARCHIVES OF ORAL BIOLOGY
Volume 110, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.archoralbio.2019.104625

Keywords

Chronic periodontitis; Inflammation; Inflammasome; Interleukin-1 beta; Mononuclear leukocyte

Funding

  1. Japan Society for the Promotion of Science, Tokyo, Japan [16K11836]
  2. Grants-in-Aid for Scientific Research [16K11836] Funding Source: KAKEN

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Objective: Accumulating evidence suggests an association between periodontitis and several systemic diseases, such as atherosclerosis. In the lesions of these diseases, nucleotide-binding domain leucine-rich repeat-containing protein 3 (NLRP3), apoptosis-associated speck-like protein containing a caspase activation and recruitment domain (ASC) and caspase-1 form inflammasome complex, which leads to the functional maturation of interleukin (IL)-1 beta via cleavage of caspase-1 in macrophages. IL-1 beta plays a critical role in the etiology of these diseases; however, inflammasome priming-specifically, IL-1 beta and NLRP3 upregulation-is necessary for effective IL-1 beta production. We investigated the effect of initial periodontal treatment on the inflammasome priming of peripheral blood mononuclear cells (PBMCs). Methods: Twenty-two patients with chronic periodontitis were enrolled in this study and given initial periodontal treatment. Peripheral blood samples were collected at baseline and re-evaluation (41.1 +/- 29.1 d after the treatment), and the relative expression of IL-1 beta, and three inflammasome components, ASC, NLRP3 and Caspase1, mRNA was determined using quantitative reverse transcription PCR. PBMCs were stimulated with silica crystals, and the IL-1 beta secretion was measured via enzyme-linked immunosorbent assay. Results: Probing pocket depth and bleeding on probing (BOP) were significantly improved after the treatment. Expression of IL-1 beta and ASC in the PBMCs decreased after the treatment. PBMCs stimulated with silica crystals secreted IL-1 beta. The treatment attenuated IL-113 secretion by PBMCs in low BOP percentages group whereas IL-1 beta secretion was increased in high BOP percentages group. Conclusion: Periodontal treatment altered the inflammasome priming status of the PBMCs, however, the effects on systemic diseases need to be further investigated.

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