Zong L, Jiang H Y
Department of Otorhinolaryngology, the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China; Department of Otorhinolaryngology Head and Neck Surgery, the First Affiliated Hospital, Sun Yat-sen University and Institute of Otorhinolaryngology, Sun Yat-sen University, Guangzhou 510080, China.
Department of Otorhinolaryngology, Hainan General Hospital, Haikou 570311, China.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020 Apr 7;55(4):371-377. doi: 10.3760/cma.j.cn115330-20190227-00099.
To investigate the feasibility of inducing human amniotic fluid stem cells into functional neurons by supporting contact co-culture depended on feeder layer from mouse vestibular supporting cells. Human amniotic fluid stem cells were isolated to culture. The vestibular tissues were obtained from the newborn C57BL/6J mouse by enzymatic digestion and cell culture, the hollow spheres were selected to prepare a monolayer feeder layer. The nGFP-labeled amniotic fluid stem cells were planted on the surface of the feeder layer to form the supporting contact co-culture without adding any exogenous nerve growth factor and neuronal signal inducing factor, and detected the expression of Tuj1 and PSD95, and investigated whether there were ion channels in neurons by FM1-43. Human amniotic fluid stem cells and mouse vestibular supporting cells, which were differentiated separately, and Transwell coculture was used as the control group. The feeder layer expressed the special marker P27(kip1)of the inner ear supporting cell. The nGFP-labeled amniotic fluid stem cells were inoculated on the feeder layer, and (52.0±3.0)% of the nGFP cells expressed Tuj1,which had typical neurons morphological characteristics[protrusion length (110.7±6.2) μm]; the feeder layer cells were differentiated separately, of which (1.1±0.6) % expressed Tuj1 in the control group; the amniotic fluid stem cells were differentiated independently without typical neuron morphological features [protrusion length (16±4.1) μm], of which (92.0±1.0) % expressed Tuj1. The amniotic fluid stem cells and the feeder layer were co-cultured in Transwell: although (92.0±1.0)% of amniotic fluid stem cells had the expression of Tuj1, which had no typical neurons morphological feature[protrusion length (17±4.5) μm], only (1.2±0.9) % of Tuj1 were observed in the feeder layer. By supporting contact co-culture, the feeder layer from the vestibular supporting cells can successfully differentiate human amniotic fluid stem cells into neurons.
通过支持性接触共培养,依赖小鼠前庭支持细胞的饲养层诱导人羊水干细胞分化为功能性神经元,探讨其可行性。分离人羊水干细胞进行培养。通过酶消化和细胞培养从新生C57BL/6J小鼠获取前庭组织,选择中空球体制备单层饲养层。将nGFP标记的羊水干细胞接种于饲养层表面,形成支持性接触共培养,不添加任何外源性神经生长因子和神经元信号诱导因子,检测Tuj1和PSD95的表达,并通过FM1-43研究神经元中是否存在离子通道。将分别分化的人羊水干细胞和小鼠前庭支持细胞进行Transwell共培养作为对照组。饲养层表达内耳支持细胞的特异性标志物P27(kip1)。将nGFP标记的羊水干细胞接种于饲养层,(52.0±3.0)%的nGFP细胞表达Tuj1,具有典型神经元形态特征[突起长度(110.7±6.2)μm];单独分化的饲养层细胞,对照组中(1.1±0.6)%表达Tuj1;独立分化的羊水干细胞无典型神经元形态特征[突起长度(16±4.1)μm],其中(92.0±1.0)%表达Tuj1。羊水干细胞与饲养层在Transwell中共培养:虽然(92.0±1.0)%的羊水干细胞有Tuj1表达,但无典型神经元形态特征[突起长度(17±4.5)μm],饲养层中仅观察到(1.2±0.9)%的Tuj1。通过支持性接触共培养,前庭支持细胞的饲养层可成功将人羊水干细胞分化为神经元。