Dental Research Institute, Department of Oral Physiology, Seoul National University School of Dentistry, Yeongun-dong, Jongno-gu, Republic of Korea.
J Dent Res. 2010 Feb;89(2):180-5. doi: 10.1177/0022034509354720. Epub 2009 Dec 29.
Although pulp fibroblasts are a major cell type in dental pulp, their roles in microbial recognition and pulpal inflammation are not well-understood. Considering the pivotal role of Toll-like receptors (TLRs) in the recognition of micro-organisms, we hypothesized that TLRs on pulp fibroblasts may induce inflammatory signals in dental pulp. In human pulp fibroblasts, TLR2, 3, 4, and 5 were constitutively expressed. Stimulation of TLR2 and 3 induced the expression of pro-inflammatory genes such as CXCL10, CCL5, and/or Cox-2 in pulp fibroblasts. Interestingly, histamine synergistically activated TLR2-mediated Cox-2 expression and PGE(2) production. The synergistic effect of histamine is mediated by histamine receptor-1 (H1R). Studies on the intra-cellular signaling pathways revealed that p38 activation is required for the synergistic activation of Cox-2 by TLR2 and histamine. Analysis of these data suggests that TLR2 on pulp fibroblasts, in concert with H1R, can induce an inflammatory response during microbial infection in dental pulp.
虽然牙髓成纤维细胞是牙髓中的主要细胞类型,但它们在微生物识别和牙髓炎症中的作用尚未完全阐明。鉴于 Toll 样受体 (TLR) 在识别微生物中的关键作用,我们假设牙髓成纤维细胞上的 TLR 可能会在牙髓中诱导炎症信号。在人牙髓成纤维细胞中,TLR2、3、4 和 5 持续表达。TLR2 和 3 的刺激诱导牙髓成纤维细胞中促炎基因如 CXCL10、CCL5 和/或 Cox-2 的表达。有趣的是,组胺协同激活 TLR2 介导的 Cox-2 表达和 PGE2 的产生。组胺的协同作用是通过组胺受体-1 (H1R) 介导的。对细胞内信号通路的研究表明,p38 的激活是 TLR2 和组胺协同激活 Cox-2 所必需的。对这些数据的分析表明,牙髓成纤维细胞上的 TLR2 与 H1R 一起,可以在微生物感染期间诱导牙髓中的炎症反应。