Clinic for Conservative Dentistry and Periodontology, School of Dental Medicine, Christian-Albrecht's University, Kiel, Germany.
Oral Medicine and Periodontology Department, Faculty of Oral and Dental Medicine, Cairo University, Cairo, Egypt.
J Clin Periodontol. 2020 Aug;47(8):991-1005. doi: 10.1111/jcpe.13323. Epub 2020 Jun 11.
Toll-like receptors are key players in mesenchymal stem/progenitor cells' micro-environmental crosstalk, endorsing various biological reactions. For the first time, this study investigates the effects of TLR3-ligation on gingival mesenchymal stem/progenitor cells (G-MSCs) stemness and differentiation properties.
G-MSCs (n = 5) were isolated, sorted using anti-STRO-1 antibodies,and sowed on culture dishes to generate colony-forming units (CFUs), and their stem/progenitor cells' features and TLR3 expression were characterized. Subsequently, TLR3 activation of G-MSCs via Poly (I:C) was done, followed by an analysis of the expression of pluripotency-related factors, mesenchymal stemness-associated surface markers, and the ability to form CFUs and multilineage differentiation, using qualitative and quantitative histochemistry and RT-PCR.
G-MSCs demonstrated all predefined stem/progenitor cells' characteristics and TLR3 expression. TLR3-activated G-MSCs showed a significantly reduced ability to form CFUs and pluripotency transcriptional factors expression. Mesenchymal stem/progenitor cell-associated surface markers and multilinear differentiation potential were significantly higher following TLR3 ligation (p < .05, Wilcoxon signed rank test).
TLR3-mediated activation maintains the mesenchymal stem/progenitor cells phenotype and drives G-MSCs' differentiation and commitment, with a shift away from an undifferentiated pluripotent cellular phenotype. This distinctive modulation could influence potential therapeutic applications of G-MSCs.
Toll 样受体是间充质干细胞/祖细胞微环境串扰中的关键参与者,促进各种生物学反应。本研究首次探讨了 TLR3 配体对牙龈间充质干细胞/祖细胞(G-MSCs)干性和分化特性的影响。
分离 G-MSCs(n=5),使用抗 STRO-1 抗体进行分选,并播种于培养皿中以生成集落形成单位(CFU),并对其干细胞/祖细胞特征和 TLR3 表达进行表征。随后,通过 Poly(I:C)激活 G-MSCs 的 TLR3,然后通过定性和定量组织化学和 RT-PCR 分析多能性相关因子、间充质干细胞相关表面标志物的表达以及 CFU 形成和多系分化的能力。
G-MSCs 表现出所有预先定义的干细胞/祖细胞特征和 TLR3 表达。TLR3 激活的 G-MSCs 形成 CFU 的能力和多能性转录因子表达显著降低。TLR3 配体后,间充质干细胞/祖细胞相关表面标志物和多线性分化潜能显著升高(p<.05,Wilcoxon 符号秩检验)。
TLR3 介导的激活维持间充质干细胞/祖细胞表型,并驱动 G-MSCs 的分化和定向,从未分化的多能细胞表型转变。这种独特的调节可能会影响 G-MSCs 的潜在治疗应用。