Xie H, Dubey N, Shim W, Ramachandra C J A, Min K S, Cao T, Rosa V
1 Oral Sciences, Faculty of Dentistry, National University of Singapore, Singapore.
2 National Heart Research Institute Singapore, National Heart Centre Singapore, Singapore.
J Dent Res. 2018 Jan;97(1):77-83. doi: 10.1177/0022034517730026. Epub 2017 Sep 12.
The induced pluripotent stem cells (iPSCs) have an intrinsic capability for indefinite self-renewal and large-scale expansion and can differentiate into all types of cells. Here, we tested the potential of iPSCs from dental pulp stem cells (DPSCs) to differentiate into functional odontoblasts. DPSCs were reprogrammed into iPSCs via electroporation of reprogramming factors OCT-4, SOX2, KLF4, LIN28, and L-MYC. The iPSCs presented overexpression of the reprogramming genes and high protein expressions of alkaline phosphatase, OCT4, and TRA-1-60 in vitro and generated tissues from 3 germ layers in vivo. Dentin discs with poly-L-lactic acid scaffolds containing iPSCs were implanted subcutaneously into immunodeficient mice. After 28 d from implantation, the iPSCs generated a pulp-like tissue with the presence of tubular dentin in vivo. The differentiation potential after long-term expansion was assessed in vitro. iPSCs and DPSCs of passages 4 and 14 were treated with either odontogenic medium or extract of bioactive cement for 28 d. Regardless of the passage tested, iPSCs expressed putative markers of odontoblastic differentiation and kept the same mineralization potential, while DPSC P14 failed to do the same. Analysis of these data collectively demonstrates that human iPSCs can be a source to derive human odontoblasts for dental pulp research and test bioactivity of materials.
诱导多能干细胞(iPSC)具有无限自我更新和大规模扩增的内在能力,并且能够分化为所有类型的细胞。在此,我们测试了来自牙髓干细胞(DPSC)的iPSC分化为功能性成牙本质细胞的潜力。通过对重编程因子OCT-4、SOX2、KLF4、LIN28和L-MYC进行电穿孔,将DPSC重编程为iPSC。这些iPSC在体外表现出重编程基因的过表达以及碱性磷酸酶、OCT4和TRA-1-60的高蛋白表达,并且在体内能够生成来自3个胚层的组织。将含有iPSC的聚-L-乳酸支架的牙本质盘皮下植入免疫缺陷小鼠体内。植入后28天,iPSC在体内生成了带有管状牙本质的牙髓样组织。在体外评估了长期扩增后的分化潜力。对第4代和第14代的iPSC和DPSC用成牙诱导培养基或生物活性水泥提取物处理28天。无论测试的代数如何,iPSC都表达了成牙本质细胞分化的假定标志物并保持相同的矿化潜力,而第14代DPSC则未能如此。对这些数据的综合分析表明,人iPSC可以作为获取人成牙本质细胞用于牙髓研究和测试材料生物活性的来源。