School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, Northern Ireland.
J Endod. 2011 Apr;37(4):473-8. doi: 10.1016/j.joen.2010.12.017.
Transient receptor potential (TRP) channels comprise a group of nonselective calcium-permeable cationic channels, which are polymodal sensors of environmental stimuli such as thermal changes and chemicals. TRPM8 and TRPA1 are cold-sensing TRP channels activated by moderate cooling and noxious cold temperatures, respectively. Both receptors have been identified in trigeminal ganglion neurones, and their expression in nonneuronal cells is now the focus of much interest. The aim of this study was to investigate the molecular and functional expression of TRPA1 and TRPM8 in dental pulp fibroblasts.
Human dental pulp fibroblasts were derived from healthy molar teeth. Gene and protein expression was determined by polymerase chain reaction and Western blotting. Cellular localization was investigated by immunohistochemistry, and TRP functionality was determined by Ca(2+) microfluorimetry.
Polymerase chain reaction and Western blotting showed gene and protein expression of both TRPA1 and TRPM8 in fibroblast cells in culture. Immunohistochemistry studies showed that TRPA1 and TRPM8 immunoreactivity co-localized with the human fibroblast surface protein. In Ca(2+) microfluorimetry studies designed to determine the functionality of TRPA1 and TRPM8 in pulp fibroblasts, we showed increased intracellular calcium (Ca(2+)) in response to the TRPM8 agonist menthol, the TRPA1 agonist cinnamaldehyde, and to cool and noxious cold stimuli, respectively. The responses to agonists and thermal stimuli were blocked in the presence of specific TRPA1 and TRPM8 antagonists.
Human dental pulp fibroblasts express TRPA1 and TRPM8 at the molecular, protein, and functional levels, indicating a possible role for fibroblasts in mediating cold responses in human teeth.
瞬时受体电位(TRP)通道组成一组非选择性钙通透性阳离子通道,其为环境刺激(如温度变化和化学物质)的多模态传感器。TRPM8 和 TRPA1 分别为中等冷却和有害冷温度激活的冷感觉 TRP 通道。这两种受体都已在三叉神经节神经元中被识别,它们在非神经元细胞中的表达现在是许多研究的重点。本研究的目的是研究牙髓成纤维细胞中 TRPA1 和 TRPM8 的分子和功能表达。
从健康磨牙中获得人牙髓成纤维细胞。通过聚合酶链反应和 Western 印迹测定基因和蛋白表达。通过免疫组织化学研究细胞定位,并通过 Ca(2+)微荧光测定法确定 TRP 功能。
聚合酶链反应和 Western 印迹显示培养中的成纤维细胞中均有 TRPA1 和 TRPM8 的基因和蛋白表达。免疫组织化学研究表明,TRPA1 和 TRPM8 免疫反应性与人类成纤维细胞表面蛋白共定位。在旨在确定牙髓成纤维细胞中 TRPA1 和 TRPM8 功能的 Ca(2+)微荧光测定研究中,我们显示出对 TRPM8 激动剂薄荷醇、TRPA1 激动剂肉桂醛以及分别对冷和有害冷刺激的细胞内钙([Ca(2+)](i))增加。在存在特异性 TRPA1 和 TRPM8 拮抗剂的情况下,对激动剂和热刺激的反应被阻断。
人牙髓成纤维细胞在分子、蛋白和功能水平上表达 TRPA1 和 TRPM8,表明成纤维细胞在介导人牙齿的冷反应中可能发挥作用。