Escobar Lina M, Escobar José Daniel, Bendahan Zita, Castellanos Jaime E
Grupo de Ortodoncia Actualizada en Investigación ORTOACTIV Facultad de Odontología, Universidad Nacional de Colombia, Bogotá, Colombia.
Grupo de Investigaciones Básicas y Aplicadas en Odontología, IBAPO Facultad de Odontología, Universidad Nacional de Colombia, Bogotá, Colombia.
J Oral Biol Craniofac Res. 2021 Apr-Jun;11(2):143-148. doi: 10.1016/j.jobcr.2021.01.002. Epub 2021 Jan 13.
Previous studies have suggested an important role of retinoic acid (RA) and ascorbic acid (AA) in the stimulation of osteoblastic differentiation; however, the function of RA and AA in the osteogenic differentiation from human dental pulp (hDPSCs) remains unclear.
This study investigated the effects of RA and AA on the differentiation of osteoblast from hDPSCs.
hDPSCs were treated with different doses of RA and AA, separately or in combination (RA + AA). Morphology and cell proliferation were assessed. Osteoblast differentiation was evaluated by alizarin red, alkaline phosphatase staining, and gene expression.
A significant reduction was observed in the number of cells treated with RA (26%) and RA + AA (30%) after 12 days of treatment. AA treatment alone induced a 12% reduction in the number of cells. Morphologically, the cells treated with RA and RA + AA were larger and more elongated than the control cells. A mesh pattern was observed in cells treated with AA. Numerous calcified nodules were present in cells treated with RA, AA, and RA + AA. This coincided with increased expression of and high alkaline phosphatase staining levels.
hDPSCs treated with RA and RA + AA showed significant reduction in proliferation, detectable morphological changes, and expression of the key differentiation gene , consistent with an osteoblast phenotype. AA induced morphological changes and early formation of calcified nodules. RA had a predominant effect when AA and RA were used together.
先前的研究表明视黄酸(RA)和抗坏血酸(AA)在刺激成骨细胞分化中起重要作用;然而,RA和AA在人牙髓干细胞(hDPSCs)成骨分化中的功能仍不清楚。
本研究调查RA和AA对hDPSCs向成骨细胞分化的影响。
hDPSCs分别用不同剂量的RA和AA单独或联合(RA + AA)处理。评估细胞形态和增殖情况。通过茜素红、碱性磷酸酶染色和基因表达评估成骨细胞分化。
处理12天后,用RA处理的细胞数量显著减少(26%),用RA + AA处理的细胞数量显著减少(30%)。单独用AA处理使细胞数量减少12%。形态上,用RA和RA + AA处理的细胞比对照细胞更大且更细长。在用AA处理的细胞中观察到网状模式。在用RA、AA和RA + AA处理的细胞中存在大量钙化结节。这与关键分化基因表达增加和碱性磷酸酶染色水平升高相一致。
用RA和RA + AA处理的hDPSCs增殖显著减少,可检测到形态变化以及关键分化基因的表达,与成骨细胞表型一致。AA诱导形态变化和钙化结节的早期形成。当AA和RA联合使用时,RA起主要作用。