Dong Qing, Wang Yuanyuan, Mohabatpour Fatemeh, Zheng Li, Papagerakis Silvana, Chen Daniel, Papagerakis Petros
Department of Orthodontics and Pediatric Dentistry, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
Department of Pediatric Dentistry, College of Stomatology, North China University of Science and Technology, Tangshan, China.
Methods Mol Biol. 2019;1922:91-101. doi: 10.1007/978-1-4939-9012-2_9.
Tissue engineering is an interdisciplinary area offering a promising approach by the use of stem cells combined with scaffolds and signaling factors for regeneration of damaged or lost tissues. Incorporation of a sufficient number of cells which do not elicit the immunoreaction in the body is a pivotal element for successful tissue formation using this method. Stem cells exhibiting strong capacity to self-renew and differentiate into different cell types are considered as a potent cell source. Among various cell sources, dental pulp stem cells (DPSCs) are widely under investigation due to the fact that they are simply obtainable from extracted third molars or orthodontically extracted teeth and show an excellent potential for clinical application and also their harvesting method is minimally invasive. DPSCs are odontogenic progenitor cells with clonogenic abilities, rapid proliferation rates, and multiple differentiation potentials. Here, we describe protocols that allow 1) the isolation of DPSCs from a single tooth; 2) the characterization of human mesenchymal stem cells markers of DPSCs by flow cytometry; 3) the culture growth of DPSCs in 2D (in cell culture flasks) and 3D (by 3D printing of cell-laden constructs); and 4) the in vivo evaluation of differentiation potential of DPSCs.
组织工程是一个跨学科领域,通过使用干细胞结合支架和信号因子为受损或缺失组织的再生提供了一种有前景的方法。使用这种方法成功形成组织的关键要素是引入足够数量且不会在体内引发免疫反应的细胞。具有强大自我更新能力并能分化为不同细胞类型的干细胞被视为一种有效的细胞来源。在各种细胞来源中,牙髓干细胞(DPSCs)受到广泛研究,因为它们可简单地从拔除的第三磨牙或正畸拔除的牙齿中获取,具有出色的临床应用潜力,并且其采集方法微创。DPSCs是具有克隆能力、快速增殖率和多种分化潜能的牙源性祖细胞。在此,我们描述了以下方案:1)从单颗牙齿中分离DPSCs;2)通过流式细胞术对DPSCs的人间充质干细胞标志物进行表征;3)在二维(细胞培养瓶中)和三维(通过对负载细胞的构建体进行3D打印)条件下培养DPSCs;4)对DPSCs的分化潜能进行体内评估。