Coelho Maria Carolina, Sanchez Paula Katherine Vargas, Fernandes Roger Rodrigo, Souza Fernanda Panzeri Pires de, Siéssere Selma, Bombonato-Prado Karina Fittipaldi
Universidade de São Paulo - USP, School of Dentistry of Ribeirão Preto, Department of Basic and Oral Biology, Ribeirão Preto, SP, Brazil.
Universidade de São Paulo - USP, School of Dentistry of Ribeirão Preto, Department of Oral and Maxillofacial Surgery and Periodontology, Ribeirão Preto, SP, Brazil.
Braz Oral Res. 2019 Feb 11;33:e013. doi: 10.1590/1807-3107bor-2019.vol33.0013.
Recent studies on functional tissue regeneration have focused on substances that favor cell proliferation and differentiation, including the bioactive phenolic compounds present in grape seed extract (GSE). The aim of this investigation was to evaluate the stimulatory potential of GSE in the functional activity of undifferentiated pulp cells and odontoblast-like cells. OD-21 and MDPC-23 cell lines were cultivated in odontogenic medium until subconfluence, seeded in 24-well culture plates in a concentration of 2x104/well and divided into: 1) OD-21 without GSE; 2) OD-21+10 µg/mL of GSE; 3) MDPC-23 without GSE; 4) MDPC-23+10 µg/mL of GSE. Cell proliferation, in situ detection of alkaline phosphatase (ALP) and total protein content were assessed after 3, 7 and 10 days, and mineralization was evaluated after 14 days. The data were analyzed by ANOVA statistical tests set at a 5% level of significance. Results revealed that cell proliferation increased after 10 days, and protein content, after 7 days of culture in MDPC-23 cells. In situ ALP staining intensity was higher in undifferentiated pulp cells and odontoblast-like cells after 7 and 10 days, respectively. A discrete increase in MDPC-23 mineralization after GSE treatment was observed despite OD-21 cells presenting a decrease in mineralized nodule deposits. Data suggest that GSE favors functional activity of differentiated cells more broadly than undifferentiated cells (OD-21). More studies with different concentrations of GSE must be conducted to confirm its benefits to cells regarding dentin regeneration.
近期关于功能性组织再生的研究聚焦于促进细胞增殖和分化的物质,包括葡萄籽提取物(GSE)中含有的生物活性酚类化合物。本研究的目的是评估GSE对未分化牙髓细胞和成牙本质样细胞功能活性的刺激潜力。将OD - 21和MDPC - 23细胞系在牙源性培养基中培养至亚汇合状态,以2×10⁴/孔的浓度接种于24孔培养板中,并分为:1)不含GSE的OD - 21;2)含10 μg/mL GSE的OD - 21;3)不含GSE的MDPC - 23;4)含10 μg/mL GSE的MDPC - 23。在3、7和10天后评估细胞增殖、碱性磷酸酶(ALP)原位检测和总蛋白含量,并在14天后评估矿化情况。数据采用设定为5%显著性水平的方差分析统计检验进行分析。结果显示,10天后细胞增殖增加,MDPC - 23细胞在培养7天后蛋白含量增加。未分化牙髓细胞和成牙本质样细胞中,原位ALP染色强度分别在7天和10天后更高。尽管OD - 21细胞矿化结节沉积减少,但观察到GSE处理后MDPC - 23矿化有离散性增加。数据表明,GSE对分化细胞功能活性的促进作用比未分化细胞(OD - 21)更广泛。必须进行更多不同浓度GSE的研究,以证实其对牙本质再生细胞的益处。