Effect of Oral Pathogens Associated With Pulpitis and Apical Periodontitis on Odontogenic Mesenchymal Stem Cells.

IF 3.3 3区 医学 Q2 CELL & TISSUE ENGINEERING
Stem Cells International Pub Date : 2025-08-31 eCollection Date: 2025-01-01 DOI:10.1155/sci/5523197
Linlong Qi, Xiaoyao Liang, Zirui Qin, Huihui Gao, Yi Zhang, Yuan Wang, Shuli Deng
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引用次数: 0

Abstract

Dental mesenchymal stem cells (MSCs) play an essential role in the development of immature permanent teeth. Bacterial infection of the pulp and periapical tissues of immature permanent teeth, the associated oral pathogens, and their virulence factors affect the viability, proliferation, differentiation, and cytokine secretion of MSCs. Bacteria and virulence factors can also trigger an inflammatory response that induces pro-inflammatory cytokine secretion and destroys odontogenic MSCs in the pulp and periapical region, negatively affecting the development of immature permanent teeth. The present study explored the role and mechanisms of oral pathogens associated with pulpitis and apical periodontitis and their virulence factors concerning odontogenic MSCs. The findings can contribute to the clinical treatment of pulpitis and apical periodontitis of immature permanent teeth, providing a theoretical basis for improving its clinical efficacy.

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牙髓炎和根尖牙周炎相关口腔病原体对牙源性间充质干细胞的影响。
牙间充质干细胞(MSCs)在未成熟恒牙的发育中起着重要的作用。未成熟恒牙牙髓和根尖周组织的细菌感染及其相关的口腔病原体及其毒力因子影响间充质干细胞的活力、增殖、分化和细胞因子分泌。细菌和毒力因子也可以引发炎症反应,诱导促炎细胞因子分泌,破坏牙髓和根尖周区域的牙源性间充质干细胞,对未成熟恒牙的发育产生负面影响。本研究旨在探讨牙髓炎和根尖牙周炎相关口腔病原体及其毒力因子在牙源性间充质干细胞中的作用和机制。本研究结果有助于临床治疗未成熟恒牙牙髓炎和根尖牙周炎,为提高其临床疗效提供理论依据。
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来源期刊
Stem Cells International
Stem Cells International CELL & TISSUE ENGINEERING-
CiteScore
8.10
自引率
2.30%
发文量
188
审稿时长
18 weeks
期刊介绍: Stem Cells International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of stem cell biology and applications. The journal will consider basic, translational, and clinical research, including animal models and clinical trials. Topics covered include, but are not limited to: embryonic stem cells; induced pluripotent stem cells; tissue-specific stem cells; stem cell differentiation; genetics and epigenetics; cancer stem cells; stem cell technologies; ethical, legal, and social issues.
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