The role of hyperglycemia in mechanisms of exacerbated inflammatory responses within the oral cavity

Cell Immunol. 2011;272(1):45-52. doi: 10.1016/j.cellimm.2011.09.008. Epub 2011 Sep 29.

Abstract

Immune modulating factors are necessary for pathogen clearance, but also contribute to host tissues damage, as those seen in periodontal diseases. Many of these responses can be exacerbated by host conditions including type 2 diabetes [T2D], where toll-like receptor 4 [TLR4] and the receptor for advanced glycated end products [RAGE] play a significant role. Here we investigate causality associated with the increase in inflammatory markers observed in periodontally diseased patients with T2D using multi-variant correlation analysis. Inflammation associated with periodontal diseases, characterized by elevated pro-inflammatory cytokines, innate immune receptor expression, and cellular infiltrate was exacerbated in patients with T2D. In addition, a feed forward loop regulated by poor glycemic control was associated with a loss of mucosal barrier integrity and accumulation of innate immune receptor ligands resulting in an exacerbation of ongoing inflammation, where RAGE and TLR4 cooperated to induce responses in oral epithelial cells, which were exacerbated by hyperglycemia.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Case-Control Studies
  • Chronic Periodontitis / complications
  • Chronic Periodontitis / immunology*
  • Chronic Periodontitis / metabolism
  • Chronic Periodontitis / pathology
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / immunology*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / pathology
  • Epithelial Cells / immunology
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Female
  • Humans
  • Hyperglycemia / complications
  • Hyperglycemia / immunology*
  • Hyperglycemia / metabolism
  • Hyperglycemia / pathology
  • Immunity, Innate / immunology*
  • Immunity, Mucosal / immunology*
  • Inflammation / complications
  • Inflammation / immunology*
  • Inflammation / metabolism
  • Inflammation / pathology
  • Ligands
  • Male
  • Middle Aged
  • Mouth / immunology*
  • Mouth / metabolism
  • Mouth / pathology
  • Primary Cell Culture
  • Receptor Cross-Talk / immunology*
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic / immunology
  • Receptors, Immunologic / metabolism
  • Signal Transduction / immunology
  • Toll-Like Receptor 4 / immunology
  • Toll-Like Receptor 4 / metabolism

Substances

  • Ligands
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic
  • TLR4 protein, human
  • Toll-Like Receptor 4