Maioli Margherita, Basoli Valentina, Santaniello Sara, Cruciani Sara, Delitala Alessandro Palmerio, Pinna Roberto, Milia Egle, Grillari-Voglauer Regina, Fontani Vania, Rinaldi Salvatore, Muggironi Roberta, Pigliaru Gianfranco, Ventura Carlo
Department of Biomedical Sciences, University of Sassari, Viale San Pietro 43/B, 07100 Sassari, Italy; Laboratory of Molecular Biology and Stem Cell Engineering, National Institute of Biostructures and Biosystems, Via Massarenti, 40138 Bologna, Italy.
Department of Biomedical Sciences, University of Sassari, Viale San Pietro 43/B, 07100 Sassari, Italy; Laboratory of Molecular Biology and Stem Cell Engineering, National Institute of Biostructures and Biosystems, Via Massarenti, 40138 Bologna, Italy; Research Department, Rinaldi Fontani Foundation, Viale Belfiore 43, 50144 Florence, Italy; Department of Biotechnology, University of Natural Resources and Life Sciences Vienna, Muthgasse 18, A-1190 Vienna, Austria.
Stem Cells Int. 2016;2016:2056416. doi: 10.1155/2016/2056416. Epub 2016 Jan 10.
Human dental pulp stem cells (hDPSCs) have shown relevant potential for cell therapy in the orthopedic and odontoiatric fields. The optimization of their osteogenic potential is currently a major challenge. Vascular endothelial growth factor A (VEGF A) has been recently reported to act as a major conductor of osteogenesis in vitro and in vivo. Here, we attempted to prime endogenous VEGF A expression without the need for viral vector mediated gene transfer technologies. We show that hDPSCs exposure to a mixture of hyaluronic, butyric, and retinoic acids (HA + BU + RA) induced the transcription of a gene program of osteogenesis and the acquirement of an osteogenic lineage. Such response was also elicited by cell exposure to melatonin, a pleiotropic agent that recently emerged as a remarkable osteogenic inducer. Interestingly, the commitment to the osteogenic fate was synergistically enhanced by the combinatorial exposure to a conditioned medium containing both melatonin and HA + BU + RA. These in vitro results suggest that in vivo osteogenesis might be improved and further studies are needed.
人牙髓干细胞(hDPSCs)在骨科和牙科学领域的细胞治疗中已显示出相关潜力。优化其成骨潜力目前是一项重大挑战。血管内皮生长因子A(VEGF A)最近被报道在体外和体内均作为成骨的主要调节因子。在此,我们试图在无需病毒载体介导的基因转移技术的情况下启动内源性VEGF A表达。我们发现,hDPSCs暴露于透明质酸、丁酸和视黄酸的混合物(HA + BU + RA)会诱导成骨基因程序的转录并获得成骨谱系。细胞暴露于褪黑素也会引发这种反应,褪黑素是一种多效性因子,最近作为一种显著的成骨诱导剂出现。有趣的是,通过联合暴露于含有褪黑素和HA + BU + RA的条件培养基,向成骨命运的定向分化得到了协同增强。这些体外结果表明,体内成骨可能会得到改善,还需要进一步研究。