Lin Xuefen, Kong Jingjing, Wu Qingting, Yang Yingying, Ji Ping
Stomatological Hospital of Shandong University, Number 44, Wen Hua Xi Lu, Shandong Province, Jinan 250012, China ; Key Laboratory of Oral Biomedicine of Shandong Province, Number 44, Wen Hua Xi Lu, Shandong Province, Jinan 250012, China.
Mediators Inflamm. 2015;2015:329405. doi: 10.1155/2015/329405. Epub 2015 Feb 24.
Accumulating evidence from previous studies suggested that interleukin-1 (IL-1β) and tumor necrosis factor-α (TNF-α) play an important role in pathogenesis of temporomandibular disorders (TMD). However, the cell surface receptors and the intracellular signal pathways leading to these cytokines expression are not fully understood. In the current study, we investigated the roles of Toll-like receptor 4 (TLR4) and its adaptor myeloid differentiation factor 88 (MyD88) in the expression of IL-1β and TNF-α in synovial fibroblasts (SFs) separated from rat temporomandibular joint (TMJ) with lipopolysaccharide (LPS) stimulation. The results showed that treatment with LPS could increase TLR4, MyD88, IL-1β, and TNF-α expression at both mRNA and protein levels. In addition, increased expression of IL-1β and TNF-α could be blocked by treatment with TAK-242, a blocker of TLR4 signaling, and also by MyD88 inhibitory peptide (MIP). These findings suggested that maybe TLR4/MyD88 signal transduction pathway participates in enhanced expression of IL-1 and TNF-α in patients with TMD. The activation of TLR4/MyD88 signal transduction pathway which results in production of proinflammatory factors may play a role in the pathogenesis of TMD.
以往研究积累的证据表明,白细胞介素-1(IL-1β)和肿瘤坏死因子-α(TNF-α)在颞下颌关节紊乱病(TMD)的发病机制中起重要作用。然而,导致这些细胞因子表达的细胞表面受体和细胞内信号通路尚未完全明确。在本研究中,我们研究了Toll样受体4(TLR4)及其接头蛋白髓样分化因子88(MyD88)在脂多糖(LPS)刺激下,对从大鼠颞下颌关节(TMJ)分离的滑膜成纤维细胞(SFs)中IL-1β和TNF-α表达的作用。结果显示,LPS处理可在mRNA和蛋白水平上增加TLR4、MyD88、IL-1β和TNF-α的表达。此外,用TLR4信号阻滞剂TAK-24以及MyD88抑制肽(MIP)处理可阻断IL-1β和TNF-α表达的增加。这些发现提示,TLR4/MyD88信号转导通路可能参与TMD患者中IL-1和TNF-α表达的增强。导致促炎因子产生的TLR4/MyD88信号转导通路的激活可能在TMD的发病机制中起作用。