Rochira Alessio, Siculella Luisa, Damiano Fabrizio, Palermo Andrea, Ferrante Franco, Carluccio Maria Annunziata, Calabriso Nadia, Giannotti Laura, Stanca Eleonora
Laboratory of Molecular Biology, Department of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy.
College of Medicine and Dentistry Birmingham, University of Birmingham, B4 6BN Birmingham, UK.
Biology (Basel). 2020 Oct 30;9(11):370. doi: 10.3390/biology9110370.
Bone regeneration is a complex process regulated by several factors that control overlapping biological processes, coordinating interactions among distinct cell populations. There is a great interest in identifying new strategies for inducing osteogenesis in a safe and efficient manner. Concentrated Growth Factor (CGF) is an autologous blood derived product obtained by centrifugation of venous blood following the procedure set on the Silfradent device. In this study the effects of CGF on osteogenic differentiation of human Bone Marrow Stem Cells (hBMSC) in vitro have been investigated; hBMSC were cultured with CGF or osteogenic medium, for 21 days. The osteogenic differentiation was evaluated measuring alkaline phosphatase (ALP) enzyme activity, matrix mineralization by alizarin red staining and through mRNA and protein quantification of osteogenic differentiation markers by Real-time PCR and Western blotting, respectively. The treatment with CGF stimulated ALP activity and promoted matrix mineralization compared to control and seems to be more effective than osteogenic medium. Also, hBMSC lost mesenchymal markers and showed other osteogenic features. Our study showed for the first time that CGF alone is able to induce osteogenic differentiation in hBMSC. The application of CGF on hBMSC osteoinduction might offer new clinical and biotechnological strategies in the tissue regeneration field.
骨再生是一个复杂的过程,受多种因素调控,这些因素控制着相互重叠的生物学过程,协调不同细胞群体之间的相互作用。人们对寻找安全有效的诱导成骨新策略有着浓厚的兴趣。浓缩生长因子(CGF)是一种自体血液衍生产品,通过按照Silfradent设备设定的程序对静脉血进行离心获得。在本研究中,研究了CGF对人骨髓干细胞(hBMSC)体外成骨分化的影响;将hBMSC与CGF或成骨培养基一起培养21天。分别通过测量碱性磷酸酶(ALP)活性、茜素红染色检测基质矿化以及通过实时PCR和蛋白质印迹法对成骨分化标志物进行mRNA和蛋白质定量来评估成骨分化。与对照组相比,CGF处理刺激了ALP活性并促进了基质矿化,并且似乎比成骨培养基更有效。此外,hBMSC失去了间充质标志物并表现出其他成骨特征。我们的研究首次表明,单独使用CGF能够诱导hBMSC的成骨分化。将CGF应用于hBMSC的骨诱导可能为组织再生领域提供新的临床和生物技术策略。