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

被引:36
作者
Amir, Jamie [1 ]
Waite, Matthew [1 ]
Tobler, Jeffrey [1 ]
Catalfamo, Dana L. [1 ,2 ]
Koutouzis, Theofilos [1 ]
Katz, Joseph [3 ]
Wallet, Shannon M. [1 ,2 ]
机构
[1] Univ Florida, Dept Periodontol, Coll Dent, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Oral Biol, Coll Dent, Gainesville, FL 32610 USA
[3] Univ Florida, Dept Oral & Maxillofacial Diagnost Sci, Coll Dent, Gainesville, FL 32610 USA
关键词
Type; 2; diabetes; Periodontal disease; Toll-like receptor 4; Receptor for advanced glycated end products; Lipopolysaccharide; N-carboxyl (methyl-lysine); Oral epithelial cells; Microbial translocation; TOLL-LIKE RECEPTORS; FACTOR-KAPPA-B; PERIODONTAL-DISEASE; DIABETES-MELLITUS; CELLS; RAGE; COMPLICATIONS; PATHOGENESIS; BACTEREMIA; ACTIVATION;
D O I
10.1016/j.cellimm.2011.09.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:45 / 52
页数:8
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