Periodontitis exacerbation during pregnancy in mice: Role of macrophage migration inhibitory factor as a key inductor

Abstract

AbstractObjectiveThe present study was designed to investigate the role of macrophage migration inhibitory factor (MIF) in the exacerbation of pregestational periodontal disease (PGPD).BackgroundPeriodontitis (PT) is a severe stage of periodontal disease characterized by inflammation of the supporting tissues of the teeth, which usually worsens during pregnancy. MIF is a proinflammatory cytokine that is significantly elevated in periodontitis, both at the beginning and at the end of pregnancy. Although periodontitis usually presents with greater severity during pregnancy, the participation of MIF in the evolution of periodontitis has not been established.MethodsTo analyze the relevance of MIF in the exacerbation of PGPD, we employed a model of PGPD in WT and Mif‐/‐ mice, both with a BALB/c genetic background. PT was induced with nylon suture ligatures placed supramarginally around the second upper right molar. For PGPD, PT was induced 2 weeks before mating. We evaluated histological changes and performed histometric analysis of the clinical attachment loss, relative expression of MMP‐2 and MMP‐13 by immunofluorescence, and relative expression of the cytokines mif, tnf‐α, ifn‐γ, and il‐17 by quantitative real‐time polymerase chain reaction (qRT‐PCR).ResultsOur data revealed that periodontal tissue from PGPD WT mice produced a twofold increase in MIF compared with PT WT mice. Moreover, the evolution of periodontitis in Mif‐/‐ mice was less severe than in PGDP WT mice. Periodontal tissue from Mif‐/‐ mice with PGPD produced 80% less TNF‐α and no IFN‐γ, as well as 50% lower expression of matrix metalloproteinase (MMP)‐2 and 25% less MMP‐13 compared to WT PGDP mice.ConclusionsOur study suggests that MIF plays an important role in the exacerbation of periodontitis during pregnancy and that MIF is partially responsible for the inflammation associated with the severity of periodontitis during pregnancy.