Horsophonphong S, Roytrakul S, Lertruangpanya K, Kitkumthorn N, Surarit R
Department of Pediatric Dentistry, Faculty of Dentistry, Mahidol University, 6 Yothi Road, Ratchathewi, Bangkok, Thailand.
Functional Proteomics Technology Laboratory, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani, Thailand.
Eur Arch Paediatr Dent. 2025 Apr 18. doi: 10.1007/s40368-025-01043-4.
The aims of this study were to identify proteomic profiles of dental pulp from deciduous teeth and compare the profiles of the two dentitions.
Teeth that were caries-free and had normal pulp conditions were collected from twelve healthy individuals. The obtained teeth consisted of deciduous teeth (n = 6) and permanent teeth (n = 6). Proteins were extracted from pulp tissue and then analysed using liquid chromatography-tandem mass spectrometry. MaxQuant was used to identify and quantify proteins from raw mass spectrometry data of the collected deciduous and previously analysed permanent dental pulp. Differentially expressed proteins (DEPs) between the dental pulp of the two dentitions were identified by a statistical analysis conducted using Metaboanalyst with criteria P-value < 0.05 and fold change > 2.
A total of 3,636 proteins were identified in the dental pulp of deciduous teeth. The biological process functional classifications of these proteins were primarily concerned with cellular process, biological regulation, metabolic process and response to stimulus. Dental pulp protein profiles differed significantly between deciduous and permanent teeth, with 736 proteins being differentially expressed, the majority of which were highly expressed in the pulp of deciduous teeth. Pathway analysis indicated DEPs to be involved in tumour necrosis factor (TNF) signalling, nuclear factor kappa B signalling, and odontoclast/osteoclast differentiation.
While the dental pulp of deciduous and permanent teeth shares some characteristics, there are also significant differences in protein expression, with the TNF signalling pathway and odontoclast/osteoclast differentiation being promoted in the dental pulp of deciduous teeth.
本研究旨在确定乳牙牙髓的蛋白质组学特征,并比较两种牙列的蛋白质组学特征。
从12名健康个体中收集无龋且牙髓状况正常的牙齿。获得的牙齿包括乳牙(n = 6)和恒牙(n = 6)。从牙髓组织中提取蛋白质,然后使用液相色谱-串联质谱进行分析。使用MaxQuant从收集的乳牙和先前分析的恒牙牙髓的原始质谱数据中鉴定和定量蛋白质。使用Metaboanalyst进行统计分析,以鉴定两种牙列牙髓之间的差异表达蛋白(DEP),标准为P值<0.05且变化倍数>2。
在乳牙牙髓中总共鉴定出3636种蛋白质。这些蛋白质的生物学过程功能分类主要涉及细胞过程、生物调节、代谢过程和对刺激的反应。乳牙和恒牙的牙髓蛋白质组特征存在显著差异,有736种蛋白质差异表达,其中大多数在乳牙牙髓中高表达。通路分析表明,差异表达蛋白参与肿瘤坏死因子(TNF)信号传导、核因子κB信号传导以及破牙细胞/破骨细胞分化。
虽然乳牙和恒牙的牙髓有一些共同特征,但蛋白质表达也存在显著差异,乳牙牙髓中肿瘤坏死因子信号通路和破牙细胞/破骨细胞分化被促进。