Proteome differences of dental stem cells between permanent and deciduous teeth by data-independent acquisition proteomics.

IF 1.7 4区 生物学 Q3 BIOLOGY Open Life Sciences Pub Date : 2025-01-29 eCollection Date: 2025-01-01 DOI:10.1515/biol-2022-0998
Suping Zhang, Yuqing Liu, Jin Dong, Min Jiao, Yongchun Gu, Liling Chen, Na Yuan, Jianrong Wang, Dezhao Yang, Fanwen Meng
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Abstract

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.

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恒牙和乳牙牙干细胞蛋白质组学研究
牙髓干细胞在牙齿再生和修复方面具有重要的应用前景。然而,全面了解牙髓干细胞(DPSC,来自恒牙)和人类脱落乳牙干细胞(SHED,来自乳牙)之间的分子差异仍然是难以实现的,这对于优化它们的治疗潜力至关重要。为了解决这一差距,我们采用了一种新的数据独立获取(DIA)蛋白质组学方法来比较DPSC和SHED的蛋白质表达谱。基于纳米lc -MS/MS DIA蛋白质组学,我们在两种细胞类型中鉴定了7000多种蛋白质。通过比较它们的表达水平,鉴定出209个差异表达蛋白。随后的基因本体和京都基因与基因组百科全书的富集分析,以及蛋白质相互作用网络的构建,揭示了显著的代谢差异和关键的调控节点。DPSC中NDUFB家族、SMARC家族、RPTOR和TLR3等蛋白的表达明显增加。已知这些蛋白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显示参与甘油脂代谢和成脂分化的AKR1B家族以及与产热相关的PRKG1、MGLL和UQCRB蛋白的表达升高。这些发现突出了DPSC和SHED的特定蛋白质组学景观,表明它们具有独特的生物学作用和潜在的应用前景。
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来源期刊
CiteScore
2.50
自引率
4.50%
发文量
131
审稿时长
43 weeks
期刊介绍: Open Life Sciences (previously Central European Journal of Biology) is a fast growing peer-reviewed journal, devoted to scholarly research in all areas of life sciences, such as molecular biology, plant science, biotechnology, cell biology, biochemistry, biophysics, microbiology and virology, ecology, differentiation and development, genetics and many others. Open Life Sciences assures top quality of published data through critical peer review and editorial involvement throughout the whole publication process. Thanks to the Open Access model of publishing, it also offers unrestricted access to published articles for all users.
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