Zhou Jun-Mei, Xing Feng-Ying, Shi Jian-Jun, Fang Zhen-Fu, Chen Xue-Jin, Chen Fang
Center for Developmental Biology, Department of Urology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, 1665 Kong Jian Road, Shanghai 200092, PR China.
Cell Biol Int. 2008 Sep;32(9):1169-75. doi: 10.1016/j.cellbi.2008.04.025. Epub 2008 May 9.
Mouse embryonic stem (ES) cells can be differentiated into neural lineage cells, but the differentiation efficiency remains low. This study revealed two important factors that influence the neural differentiation efficiency of mouse ES cells: the first is the quality of embryonic bodies (EBs); good quality of EBs consistently originated from a suspension culture of 1x10(5) ES cells/ml serum-free chemically defined neural inducing medium and they exhibited a smooth round shape, with a dark central region surrounded by a light band. Such EBs are capable of attaining high neural differentiation efficiency. However, poor quality EBs originated from a suspension culture of 1x10(6) ES cells/ml serum-free chemically defined neural inducing medium and exhibited an irregular shape or adhered to the bottom of the dish; they displayed low neural differentiation efficiency. The second factor is the seeding density of EBs: a low seeding density (5 EBs/cm2) induced cells to differentiate into a more caudalized subtypes compared to the cells obtained from high seeding density (20 EBs/cm2). These findings provided fresh insight into the neural induction of mouse ES cells.
小鼠胚胎干细胞(ES细胞)可分化为神经谱系细胞,但分化效率仍然较低。本研究揭示了影响小鼠ES细胞神经分化效率的两个重要因素:第一个是胚体(EBs)的质量;高质量的EBs一直来源于1×10⁵个ES细胞/ml无血清化学限定神经诱导培养基的悬浮培养,它们呈现出光滑的圆形,中央区域较暗,周围有一条亮带。这样的EBs能够获得较高的神经分化效率。然而,低质量的EBs来源于1×10⁶个ES细胞/ml无血清化学限定神经诱导培养基的悬浮培养,呈现出不规则形状或附着于培养皿底部;它们的神经分化效率较低。第二个因素是EBs的接种密度:与高接种密度(20个EBs/cm²)获得的细胞相比,低接种密度(5个EBs/cm²)诱导细胞分化为更向尾侧化的亚型。这些发现为小鼠ES细胞的神经诱导提供了新的见解。