Department of Bioscience Research, College of Dentistry, University of Tennessee Health Science Center, Memphis, TN, USA.
Department of Endodontics, Boston University Henry M. Goldman School of Dental Medicine, Boston, MA, USA.
J Tissue Eng Regen Med. 2018 Apr;12(4):e1836-e1851. doi: 10.1002/term.2615. Epub 2018 Jan 17.
Induced pluripotent stem cells (iPSCs) give rise to neural stem/progenitor cells, serving as a good source for neural regeneration. Here, we established transgene-free (TF) iPSCs from dental stem cells (DSCs) and determined their capacity to differentiate into functional neurons in vitro. Generated TF iPSCs from stem cells of apical papilla and dental pulp stem cells underwent two methods-embryoid body-mediated and direct induction, to guide TF-DSC iPSCs along with H9 or H9 Syn-GFP (human embryonic stem cells) into functional neurons in vitro. Using the embryoid body-mediated method, early stage neural markers PAX6, SOX1, and nestin were detected by immunocytofluorescence or reverse transcription-real time polymerase chain reaction (RT-qPCR). At late stage of neural induction measured at Weeks 7 and 9, the expression levels of neuron-specific markers Nav1.6, Kv1.4, Kv4.2, synapsin, SNAP25, PSD95, GAD67, GAP43, and NSE varied between stem cells of apical papilla iPSCs and H9. For direct induction method, iPSCs were directly induced into neural stem/progenitor cells and guided to become neuron-like cells. The direct method, while simpler, showed cell detachment and death during the differentiation process. At early stage, PAX6, SOX1 and nestin were detected. At late stage of differentiation, all five genes tested, nestin, βIII-tubulin, neurofilament medium chain, GFAP, and Nav, were positive in many cells in cultures. Both differentiation methods led to neuron-like cells in cultures exhibiting sodium and potassium currents, action potential, or spontaneous excitatory postsynaptic potential. Thus, TF-DSC iPSCs are capable of undergoing guided neurogenic differentiation into functional neurons in vitro, thereby may serve as a cell source for neural regeneration.
诱导多能干细胞(iPSCs)分化为神经干细胞/祖细胞,是神经再生的良好来源。本研究从牙髓干细胞(DPSCs)中建立了无转基因(TF)iPSCs,并确定了它们在体外分化为功能性神经元的能力。从根尖乳头干细胞和牙髓干细胞生成的 TF-iPSCs 通过两种方法-胚状体介导和直接诱导,指导 TF-DSC-iPSCs 与 H9 或 H9Syn-GFP(人胚胎干细胞)一起在体外分化为功能性神经元。通过胚状体介导的方法,免疫细胞荧光或逆转录实时聚合酶链反应(RT-qPCR)检测早期神经标志物 PAX6、SOX1 和巢蛋白。在第 7 周和第 9 周的晚期神经诱导阶段,神经元特异性标志物 Nav1.6、Kv1.4、Kv4.2、突触素、SNAP25、PSD95、GAD67、GAP43 和 NSE 的表达水平在根尖乳头 iPSCs 和 H9 之间有所不同。对于直接诱导方法,iPSCs 直接诱导为神经干细胞/祖细胞,并指导其成为神经元样细胞。直接方法虽然更简单,但在分化过程中会出现细胞脱落和死亡。在早期,检测到 PAX6、SOX1 和巢蛋白。在分化的晚期,所有测试的五个基因,巢蛋白、βIII-微管蛋白、神经丝中等链、GFAP 和 Nav,在培养物中的许多细胞中呈阳性。两种分化方法都导致培养物中的神经元样细胞表现出钠和钾电流、动作电位或自发性兴奋性突触后电位。因此,TF-DSC-iPSCs 能够在体外进行神经发生分化为功能性神经元,从而可能成为神经再生的细胞来源。