Orthodontic cell stress modifies proinflammatory cytokine expression in human PDL cells and induces immunomodulatory effects via TLR-4 signaling in vitro

被引:14
|
作者
Marciniak, Jana [1 ,2 ]
Lossdoerfer, Stefan [2 ]
Knaup, Isabel [1 ]
Bastian, Asisa [1 ]
Craveiro, Rogerio B. [1 ]
Jaeger, Andreas [2 ]
Wolf, Michael [1 ]
机构
[1] Univ Aachen, Dept Orthodont, Dent Clin, Pauwelsstr 30, D-52074 Aachen, Germany
[2] Univ Bonn, Dept Orthodont, Dent Clin, Bonn, Germany
关键词
Mechanical loading; hPDL cells; TLR-4; signaling; Interaction with immune cells; PERIODONTAL-LIGAMENT CELLS; PATTERN-RECOGNITION RECEPTORS; PRO-INFLAMMATORY CYTOKINES; TOOTH MOVEMENT VELOCITY; ALVEOLAR BONE LOSS; FACTOR-KAPPA-B; CREVICULAR FLUID; HUMAN GINGIVAL; ACTIVATION; TRANSDUCTION;
D O I
10.1007/s00784-019-03111-8
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective Biomechanical orthodontics loading of the periodontium initiates a cascade of inflammatory signaling events that induce periodontal remodeling and finally facilitate orthodontic tooth movement. Pattern recognition receptors such as toll-like receptors (TLRs) have been well characterized for their ability to induce the activation of inflammatory, immunomodulatory cytokines. Here, we examined whether the cellular response of human periodontal ligament (hPDL) cells to mechanical stress involves TLR-4 signaling in vitro. Materials and methods Confluent hPDL cells were cultured in the presence of 5 mu g/ml TLR-4 antibody (TLR-4ab) for 1 h prior to the induction of compressive forces by the use of round glass plates for 24 h. At harvest, interleukin-6 and interleukin-8 (IL-6, IL-8) mRNA and protein expression were analyzed by real-time PCR and ELISA. The immunomodulatory role of mechanical cell stress and TLR-4 signaling was addressed in co-culture experiments of hPDL and THP-1 cells targeting monocyte adhesion and by culturing osteoclastic precursors (RAW 264.7) in the presence of the conditioned medium of hPDL cells that had been mechanically loaded before. Results Basal expression of IL-6 and IL-8 was not affected by TLR-4ab, but increased significantly upon mechanical loading of hPDL cells. When cells were mechanically stressed in the presence of TLR-4ab, the effect seen for loading alone was markedly reduced. Likewise, monocyte adhesion and osteoclastic differentiation were enhanced significantly by mechanical stress of hPDL cells and this effect was partially inhibited by TLR-4ab. Conclusions The results of the present study indicate a proinflammatory and immunomodulatory influence of mechanical loading on hPDL cells. Intracellular signaling involves a TLR-4-dependent pathway.
引用
收藏
页码:1411 / 1419
页数:9
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