Zhang Suping, Liu Yuqing, Dong Jin, Jiao Min, Gu Yongchun, Chen Liling, Yuan Na, Wang Jianrong, Yang Dezhao, Meng Fanwen
Infectious Disease Prevention and Control Department, Suzhou Center for Disease Control and Prevention, Suzhou 215131, China.
Cyrus Tang Medical Institute, Soochow University School of Medicine, Suzhou 215123, China.
Open Life Sci. 2025 Jan 29;20(1):20220998. doi: 10.1515/biol-2022-0998. eCollection 2025.
Dental pulp stem cells hold significant prospects for tooth regeneration and repair. However, a comprehensive understanding of the molecular differences between dental pulp stem cells (DPSC, from permanent teeth) and stem cells from human exfoliated deciduous teeth (SHED, from deciduous teeth) remains elusive, which is crucial for optimizing their therapeutic potential. To address this gap, we employed a novel data-independent acquisition (DIA) proteomics approach to compare the protein expression profiles of DPSC and SHED. Based on nano-LC-MS/MS DIA proteomics, we identified over 7,000 proteins in both cell types. By comparing their expression levels, 209 differentially expressed proteins were identified. Subsequent Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses, along with protein-protein interaction network construction, revealed significant metabolic differences and key regulatory nodes. DPSC exhibited significantly higher expression of proteins belonging to the NDUFB family, SMARC family, RPTOR and TLR3. These proteins are known to be involved in critical cellular processes such as mitochondrial energy metabolism, mTOR-related autophagy pathway, and innate immune response. Conversely, SHED displayed elevated expression of AKR1B family, which participated in glycerolipid metabolism and adipogenic differentiation, PRKG1, MGLL and UQCRB proteins associated with thermogenesis. These findings highlight the specific proteomic landscape of DPSC and SHED, suggesting their distinct biological roles and potential applications.
牙髓干细胞在牙齿再生和修复方面具有巨大的前景。然而,对于牙髓干细胞(来自恒牙的DPSC)和人脱落乳牙干细胞(来自乳牙的SHED)之间分子差异的全面理解仍然难以捉摸,而这对于优化它们的治疗潜力至关重要。为了填补这一空白,我们采用了一种新型的数据非依赖采集(DIA)蛋白质组学方法来比较DPSC和SHED的蛋白质表达谱。基于纳升液相色谱-串联质谱(nano-LC-MS/MS)DIA蛋白质组学,我们在两种细胞类型中鉴定出了7000多种蛋白质。通过比较它们的表达水平,鉴定出了209种差异表达蛋白质。随后的基因本体论和京都基因与基因组百科全书富集分析,以及蛋白质-蛋白质相互作用网络构建,揭示了显著的代谢差异和关键调控节点。DPSC表现出属于NDUFB家族、SMARC家族、RPTOR和TLR3的蛋白质表达显著更高。已知这些蛋白质参与关键的细胞过程,如线粒体能量代谢、mTOR相关的自噬途径和先天免疫反应。相反,SHED显示出AKR1B家族的表达升高,该家族参与甘油脂质代谢和成脂分化,以及与产热相关的PRKG1、MGLL和UQCRB蛋白质。这些发现突出了DPSC和SHED特定的蛋白质组学特征,表明它们具有不同的生物学作用和潜在应用。