Paquet-Durand François, Tan Saime, Bicker Gerd
Physiologisches Institut, Abteilung Zellbiologie, Tierärztliche Hochschule Hannover, Bischofsholer Damm 15, D-30559, Hannover, Germany.
Brain Res Dev Brain Res. 2003 May 14;142(2):161-7. doi: 10.1016/s0165-3806(03)00065-8.
Cells from the human teratocarcinoma line NTera-2 can be induced to terminally differentiate into postmitotic neurons when treated with retinoic acid. However, this differentiation process is rather time consuming as it takes between 42 and 54 days. Here, we propose a modified differentiation protocol which reduces the time needed for differentiation considerably without compromising the quantity of the neurons obtained. The introduction of a proliferation step as free floating cell spheres cuts the total time needed to obtain high yields of purified NT-2 neurons to about 24-28 days. The cells obtained show neuronal morphology and migrate to form ganglion-like cell conglomerates. Differentiated cells express neuronal polarity markers such as the cytoskeleton associated proteins MAP2 and Tau. Moreover, the generation of neurons in sphere cultures induced immunoreactivity to the ELAV-like neuronal RNA-binding proteins HuC/D, which have been implicated in mechanisms of nerve cell differentiation.
人畸胎瘤细胞系NTera-2的细胞在用视黄酸处理时可被诱导终末分化为有丝分裂后神经元。然而,这个分化过程相当耗时,因为需要42到54天。在此,我们提出一种改良的分化方案,该方案可大幅减少分化所需时间,同时不影响获得的神经元数量。引入一个作为自由漂浮细胞球的增殖步骤,可将获得高产率纯化NT-2神经元所需的总时间缩短至约24 - 28天。获得的细胞呈现神经元形态,并迁移形成神经节样细胞团块。分化细胞表达神经元极性标记物,如细胞骨架相关蛋白MAP2和Tau。此外,球状体培养中神经元的生成诱导了对ELAV样神经元RNA结合蛋白HuC/D的免疫反应性,这些蛋白与神经细胞分化机制有关。