Zhao Penglai, Zhu Tongming, Lu Xiaocheng, Zhu Jianhong, Li Lixin
Department of Neurosurgery, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu, China; Department of Neurosurgery, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing 210029, Jiangsu, China.
Department of Neurosurgery, Fudan university Huashan Hospital, Shanghai 200040, China.
Brain Res. 2015 Jul 30;1615:51-60. doi: 10.1016/j.brainres.2015.04.027. Epub 2015 Apr 24.
Direct lineage reprogramming of human fibroblasts into functional neurons holds great promise for biomedical applications such as regenerative medicine and cellbased disease modelling. However, clinical applications must consider how to increase neuronal conversion efficiency and at the same time reduce the number of required transcription factors. Here, we investigated whether Neurogenin 2 (Ngn2), which is a proneural gene that directs neuronal differentiation of progenitor cells during development, can enhance the generation of patient-specific induced neuronal cells. In this study, we transfected Ascl1, Sox2 and Ngn2 into human fibroblasts from the patients' scalp by lentivirus. Morphological analysis, immunocytochemistry, gene expression and electrophysiological analysis were performed to identify the similarity of induced neuronal cells (iNCs) to human neuronal cells. Ngn2 increase the conversion efficiency from 4% to 13.4%. iNCs express neuronal cell markers and resemble wild-type neurons in their morphology, gene expression profiles and exhibit functional membrane properties of mature neurons. Implanted iNCs can survive and integrate in mouse brains and, unlike iPS cell-derived neural cells, do not generate tumours.
将人类成纤维细胞直接重编程为功能性神经元,在再生医学和基于细胞的疾病建模等生物医学应用方面具有巨大潜力。然而,临床应用必须考虑如何提高神经元转化效率,同时减少所需转录因子的数量。在此,我们研究了神经生成素2(Ngn2),它是一种在发育过程中指导祖细胞神经元分化的神经前体细胞基因,是否能够增强患者特异性诱导神经元细胞的生成。在本研究中,我们通过慢病毒将Ascl1、Sox2和Ngn2转染到取自患者头皮的人类成纤维细胞中。通过形态学分析、免疫细胞化学、基因表达和电生理分析来鉴定诱导神经元细胞(iNCs)与人类神经元细胞的相似性。Ngn2将转化效率从4%提高到了13.4%。iNCs表达神经元细胞标志物,在形态、基因表达谱方面与野生型神经元相似,并表现出成熟神经元的功能性膜特性。植入的iNCs能够在小鼠大脑中存活并整合,并且与诱导多能干细胞衍生的神经细胞不同,不会产生肿瘤。