Ballikaya Elif, Babadag Sena, San Keskin Nalan Oya, Çelebi-Saltik Betül
Department of Oral and Dental Health Research, Hacettepe University Graduate School of Health Sciences, Ankara, Turkey.
Department of Pediatric Dentistry, Hacettepe University Faculty of Dentistry, Ankara, Turkey.
Acta Stomatol Croat. 2024 Mar;58(1):2-17. doi: 10.15644/asc58/1/1.
This study aimed to evaluate the biological effects of "proanthocyanidin" (PA), and "nisin" (Ni), on dental pulp stem cells (DPSCs) and LPS-induced DPSCs as well as their antimicrobial effects against and .
After characterization of DPSCs, cytotoxicity of PA and Ni on DPSCs were evaluated using a water-soluble tetrazolium salt (WST-1). The cytokines and chemokines released by DPSCs and the expression levels of IL-6, IL-8, and TNF alpha were detected with human Cytokine Array C5 and enzyme-linked immunosorbent assay (ELİSA), respectively. The antibacterial activities of PA and Ni were tested using the drop plate method.
PA at 75 μg/ml increased cell viability, decreased TNF-α expression of DPSCs, did not show any cytotoxic effects on LPS-induced DPSCs, and also showed a tendency to decrease TNF-α expression. PA at 75 μg/ml exhibited higher expressions of TIMP-2, OPG, IL-7, and IL-8 in LPS-induced DPSCs compared to DPSCs. Ni at 100 μg/ml decreased TNF-α expression in DPSCs with no cytotoxic effects. It provided increased cell viability and a downregulation trend of TNF-α expression in LPS-induced DPSCs. Both Ni and PA provided strong antibacterial effects against . Ni at 200μg/ml had strong antibacterial effects against without affecting negatively the viability of both DPSCs and LPS-induced DPSCs and showed anti-inflammatory activity by decreasing TNF-α expression. PA provided strong antibacterial effects against at 200 μg/ml but affected DPSCs viability negatively.
PA and Ni at specific concentrations exhibited immunomodulatory activity on DPSCs and LPS-induced DPSCs without any cytotoxic effects and strong antibacterial effects on .
本研究旨在评估原花青素(PA)和乳酸链球菌素(Ni)对牙髓干细胞(DPSC)以及脂多糖(LPS)诱导的DPSC的生物学效应,及其对[具体细菌名称1]和[具体细菌名称2]的抗菌作用。
对DPSC进行鉴定后,使用水溶性四氮唑盐(WST-1)评估PA和Ni对DPSC的细胞毒性。分别用人细胞因子阵列C5和酶联免疫吸附测定(ELISA)检测DPSC释放的细胞因子和趋化因子以及白细胞介素-6(IL-6)、白细胞介素-8(IL-8)和肿瘤坏死因子-α(TNF-α)的表达水平。采用点滴平板法检测PA和Ni的抗菌活性。
75μg/ml的PA可提高细胞活力,降低DPSC的TNF-α表达,对LPS诱导的DPSC无任何细胞毒性作用,且有降低TNF-α表达的趋势。与DPSC相比,75μg/ml的PA使LPS诱导的DPSC中金属蛋白酶组织抑制因子-2(TIMP-2)、骨保护素(OPG)、IL-7和IL-8的表达更高。100μg/ml的Ni可降低DPSC中TNF-α的表达,无细胞毒性作用。它提高了细胞活力,并使LPS诱导的DPSC中TNF-α表达呈下调趋势。Ni和PA对[具体细菌名称1]均有较强的抗菌作用。200μg/ml的Ni对[具体细菌名称2]有较强的抗菌作用,且不影响DPSC和LPS诱导的DPSC的活力,并通过降低TNF-α表达显示出抗炎活性。200μg/ml的PA对[具体细菌名称2]有较强的抗菌作用,但对DPSC的活力有负面影响。
特定浓度的PA和Ni对DPSC以及LPS诱导的DPSC具有免疫调节活性,无任何细胞毒性作用,且对[具体细菌名称1]和[具体细菌名称2]有较强的抗菌作用。