Dai XueLiang, Lu XiaoCheng, Cheng Feng, Hao HuaiYong, Qian TengDa, Yu Wan, Tang LinJun, Li LiXin
1Department of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu, China.
Int J Neurosci. 2015 May;125(5):367-74. doi: 10.3109/00207454.2014.935375. Epub 2014 Aug 19.
Skin-derived precursors (SKPs), a novel stem cell population isolated from mammalian skin, can differentiate into neural and mesodermal lineages. Cell therapy using SKPs seems like a promising approach for the treatment of neural diseases, however, the low efficiency of neuronal differentiation limited their clinical application. In the present study, we transfected neurogenin 2 (Ngn2), a member of the bHLH transcription factor family, into SKPs by lentivirus. Morphological analysis, immunocytochemistry, Western blot, and electrophysiological analysis were performed to identify the cells derived from SKPs following 7-14 d neural induction. The results of immunocytochemistry staining showed that expression of neuronal markers, including MAP2, NF and NeuN were significantly elevated compared with those in GFP-SKPs and parental SKPs. Western blot confirmed the increased expression of NF-M and NeuN in Ngn2-SKPs-derived cells. Moreover, electrophysiological analysis showed that Ngn2-SKPs-derived neurons also acquired voltage-gated Na+ channels, which were absent in GFP-SKPs. Furthermore, western blot showed that Ngn2 enhanced the expression of Delta-like1, which reduced the level of Hes1 and suppressed Notch pathway. Therefore, overexpression of Ngn2 enhanced the neural differentiation of SKPs, probably through cis-inhibiting of Notch signal pathway.
皮肤源性前体细胞(SKPs)是从哺乳动物皮肤中分离出来的一种新型干细胞群体,能够分化为神经和中胚层谱系细胞。使用SKPs进行细胞治疗似乎是治疗神经疾病的一种有前景的方法,然而,神经元分化效率低下限制了它们的临床应用。在本研究中,我们通过慢病毒将bHLH转录因子家族成员神经生成素2(Ngn2)转染到SKPs中。在进行7-14天的神经诱导后,进行形态学分析、免疫细胞化学、蛋白质印迹和电生理分析,以鉴定源自SKPs的细胞。免疫细胞化学染色结果显示,与绿色荧光蛋白标记的SKPs(GFP-SKPs)和原始SKPs相比,包括微管相关蛋白2(MAP2)、神经丝蛋白(NF)和神经元核抗原(NeuN)在内的神经元标志物的表达显著升高。蛋白质印迹证实了Ngn2转染的SKPs(Ngn2-SKPs)衍生细胞中神经丝蛋白-M(NF-M)和NeuN的表达增加。此外,电生理分析表明,Ngn2-SKPs衍生的神经元也获得了电压门控钠通道,而GFP-SKPs中不存在这种通道。此外,蛋白质印迹显示,Ngn2增强了Delta样蛋白1(Delta-like1)的表达,这降低了Hes1的水平并抑制了Notch信号通路。因此,Ngn2的过表达可能通过顺式抑制Notch信号通路增强了SKPs的神经分化。