Park Ha Bin, Dinh Yen, Yesares Rubi Pilar, Gibbs Jennifer L, Michot Benoit
Department of Restorative Dentistry and Biomaterials Sciences, Harvard School of Dental Medicine, Boston, MA, United States.
PeerJ. 2024 Dec 18;12:e18742. doi: 10.7717/peerj.18742. eCollection 2024.
Propolis is a natural substance produced by honeybees that has various biological properties including, anti-inflammatory, antioxidant and antimicrobial properties. Although previous studies have evaluated the antimicrobial effects of propolis in dentistry, its effects on dental pulp stem cell (DPSC) viability, migration, and differentiation are yet not well understood. The objective of this study was to investigate the effects of Chinese propolis on viability/proliferation, migration, differentiation and cytokine expression in DPSCs.
Commercially available DPSCs (Lonza) were treated with aqueous extract of propolis (AEP) or ethanolic extract of propolis (EEP), and viability/proliferation was evaluated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assays and quantification of nuclear staining. DPSC differentiation into mineralizing cells was evaluated with Alizarin red staining and cell migration was assessed using Boyden Chamber Transwell inserts. Cytokine expression was measured by RT-qPCR. AEP and EEP at 0.03 and 0.1 mg/mL did not affect DPSC viability/proliferation for up to 7-days treatment.
Higher doses (0.33-33 mg/mL) induced a dose dependent decrease in DPSC viability/proliferation with a more prominent effect with EEP at 7 days. Neither AEP nor EEP induced DPSC differentiation into mineralizing cells, but both AEP and EEP (0.03-0.1 mg/ml) induced a dose dependent increase in DPSC migration. In addition, EEP prevents the upregulation of IL1b and IL6 but not IL8 and CCL2 in response to lipopolysaccharide stimulation. AEP has less potent anti-inflammatory effects and prevents only IL1b upregulation.
This study provides new information about the biologic properties of ethanolic and aqueous extracts of propolis and shows that propolis, at doses that do not affect cell viability, induces DPSC migration and has anti-inflammatory properties. These data highlight the potential use of propolis as an alternative intra-canal medicament for regenerative endodontic procedures.
蜂胶是蜜蜂产生的一种天然物质,具有多种生物学特性,包括抗炎、抗氧化和抗菌特性。尽管先前的研究评估了蜂胶在牙科领域的抗菌作用,但其对牙髓干细胞(DPSC)活力、迁移和分化的影响尚未完全明确。本研究的目的是探讨中国蜂胶对DPSC活力/增殖、迁移、分化和细胞因子表达的影响。
使用市售的DPSC(Lonza),用蜂胶水提取物(AEP)或蜂胶乙醇提取物(EEP)进行处理,并使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)法和细胞核染色定量评估活力/增殖。用茜素红染色评估DPSC向矿化细胞的分化,并使用Boyden小室Transwell插入物评估细胞迁移。通过RT-qPCR测量细胞因子表达。在长达7天的处理中,0.03和0.1mg/mL的AEP和EEP不影响DPSC活力/增殖。
较高剂量(0.33-33mg/mL)诱导DPSC活力/增殖呈剂量依赖性下降,7天时EEP的作用更显著。AEP和EEP均未诱导DPSC分化为矿化细胞,但AEP和EEP(0.03-0.1mg/ml)均诱导DPSC迁移呈剂量依赖性增加。此外,EEP可防止脂多糖刺激引起的IL1b和IL6上调,但不能防止IL8和CCL2上调。AEP的抗炎作用较弱,仅能防止IL1b上调。
本研究提供了有关蜂胶乙醇提取物和水提取物生物学特性的新信息,并表明在不影响细胞活力的剂量下,蜂胶可诱导DPSC迁移并具有抗炎特性。这些数据突出了蜂胶作为再生牙髓治疗中根管内替代药物的潜在用途。