Bharti Ramesh, Tikku Aseem Prakash, Verma Promila, Yadav Rakesh Kumar, Pant Aditya Bhushan
Department of Conservative Dentistry and Endodontics, Faculty of Dental Sciences, King George Medical University, Lucknow, Uttar Pradesh, India.
Department of Toxicology Research, CSIR-Indian Institute of Toxicology and Research, Lucknow, Uttar Pradesh, India.
J Conserv Dent Endod. 2024 Sep;27(9):975-982. doi: 10.4103/JCDE.JCDE_362_24. Epub 2024 Sep 7.
Platelet-rich fibrin (PRF) has been used, while concentrated growth factor (CGF) has recently evolved as a bioscaffold in regenerative endodontics.
This study aimed to evaluate the effect of PRF and CGF on the proliferation, migration, and differentiation of human-induced pluripotent stem cells (hiPSCs).
CGF and PRF were fabricated from voluntarily donated human blood, and a conditioned medium was prepared. HiPSCs were isolated and cultivated on a conditioned medium for 12 days. The proliferation rate was analyzed using a trypan blue assay on days 9, 10, and 11. The migratory rate was evaluated using a wound healing assay after 24, 48, and 72 h. For assessing the differentiation of hiPSCs, various markers with quantitative real-time polymerase chain reactions on day 12 were used.
Mesenchymal phenotypic transition was seen with an increase in proliferation rate in the PRF group more than in the CGF group on day 9, along with the differentiation of cells with an increase in osteoblastic markers on day 12 in both groups. The migratory capacity of cells was significantly increased in the CGF and PRF groups, with a greater increase in the CGF group.
CGF and PRF extend the duration of growth factor activity and enhance cell proliferation and osteogenic differentiation, with hiPSCs serving as a bioscaffold with high regenerative potential.
富血小板纤维蛋白(PRF)已被应用,而浓缩生长因子(CGF)最近已发展成为再生牙髓病学中的一种生物支架。
本研究旨在评估PRF和CGF对人诱导多能干细胞(hiPSC)增殖、迁移和分化的影响。
从自愿捐献的人血液中制备CGF和PRF,并制备条件培养基。分离hiPSC并在条件培养基上培养12天。在第9、10和11天使用台盼蓝试验分析增殖率。在24、48和72小时后使用伤口愈合试验评估迁移率。为了评估hiPSC的分化,在第12天使用定量实时聚合酶链反应检测各种标志物。
在第9天,PRF组的增殖率高于CGF组,出现间充质表型转变,并且在第12天两组中随着成骨细胞标志物的增加细胞发生分化。CGF组和PRF组细胞的迁移能力显著增加,CGF组增加更多。
CGF和PRF延长了生长因子活性的持续时间,增强了细胞增殖和成骨分化,hiPSC作为具有高再生潜力的生物支架发挥作用。