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.
Clin Oral Investig. 2024 May 17;28(6):321. doi: 10.1007/s00784-024-05698-z.
OBJECTIVES: To obtain and compare the protein profiles of supernumerary and normal permanent dental pulp tissues. MATERIALS AND METHODS: Dental pulp tissues were obtained from supernumerary and normal permanent teeth. Proteins were extracted and analyzed by liquid chromatography-tandem mass spectrometry (LC/MS-MS). Protein identification and quantification from MS data was performed with MaxQuant. Statistical analysis was conducted using Metaboanalyst to identify differentially expressed proteins (DEPs) (P-value < 0.05, fold-change > 2). Gene Ontology enrichment analyses were performed with gProfiler. RESULTS: A total of 3,534 proteins were found in normal dental pulp tissue and 1,093 in supernumerary dental pulp tissue, with 174 DEPs between the two groups. This analysis revealed similar functional characteristics in terms of cellular component organization, cell differentiation, developmental process, and response to stimulus, alongside exclusive functions unique to normal permanent dental pulp tissues such as healing, vascular development and cell death. Upon examination of DEPs, these proteins were associated with the processes of wound healing and apoptosis. CONCLUSIONS: This study provides a comprehensive understanding of the protein profile of dental pulp tissue, including the first such profiling of supernumerary permanent dental pulp. There are functional differences between the proteomic profiles of supernumerary and normal permanent dental pulp tissue, despite certain biological similarities between the two groups. Differences in protein expression were identified, and the identified DEPs were linked to the healing and apoptosis processes. CLINICAL RELEVANCE: This discovery enhances our knowledge of supernumerary and normal permanent pulp tissue, and serves as a valuable reference for future studies on supernumerary teeth.
目的:获取并比较额外和正常恒牙髓组织的蛋白质谱。
材料与方法:从额外和正常恒磨牙中获取牙髓组织。通过液相色谱-串联质谱(LC/MS-MS)提取和分析蛋白质。使用 MaxQuant 从 MS 数据中进行蛋白质鉴定和定量。使用 Metaboanalyst 进行统计分析以识别差异表达蛋白(DEPs)(P 值<0.05,倍数变化>2)。使用 gProfiler 进行基因本体富集分析。
结果:在正常牙髓组织中发现了 3534 种蛋白质,在额外牙髓组织中发现了 1093 种蛋白质,两组之间有 174 个 DEPs。该分析揭示了在细胞成分组织、细胞分化、发育过程和对刺激的反应等方面具有相似的功能特征,以及正常恒牙髓组织所特有的独特功能,如愈合、血管发育和细胞死亡。检查 DEPs 后,这些蛋白质与伤口愈合和细胞凋亡过程有关。
结论:本研究提供了对牙髓组织蛋白质谱的全面了解,包括首次对额外恒牙髓组织进行蛋白质谱分析。尽管两组之间存在某些生物学相似性,但额外和正常恒牙髓组织的蛋白质谱存在功能差异。鉴定出蛋白质表达的差异,并将鉴定出的 DEPs 与愈合和细胞凋亡过程联系起来。
临床意义:这一发现增强了我们对额外和正常恒牙髓组织的认识,为未来对额外牙齿的研究提供了有价值的参考。
Clin Oral Investig. 2024-5-17
J Periodontal Res. 2021-1
Zhonghua Kou Qiang Yi Xue Za Zhi. 2013-6
J Oral Pathol Med. 2008-10
Proteomics Clin Appl. 2025-7
Eur Arch Paediatr Dent. 2025-4-18
Clin Exp Dent Res. 2025-2
Nat Biotechnol. 2023-12
World J Biol Chem. 2021-9-27
Clin Oral Investig. 2021-12
Clin Oral Investig. 2021-5