Narayanan Gunaseelan, Yu Yuan Hong, Tham Muly, Gan Hui Theng, Ramasamy Srinivas, Sankaran Shvetha, Hariharan Srivats, Ahmed Sohail
Neural Stem Cell Laboratory, Institute of Medical Biology, Agency for Science, Technology and Research (A*STAR);
Neural Stem Cell Laboratory, Institute of Medical Biology, Agency for Science, Technology and Research (A*STAR).
J Vis Exp. 2016 Oct 4(116):54456. doi: 10.3791/54456.
Neural stem cells (NSCs) have the ability to self-renew and generate the three major neural lineages - astrocytes, neurons and oligodendrocytes. NSCs and neural progenitors (NPs) are commonly cultured in vitro as neurospheres. This protocol describes in detail how to determine the NSC frequency in a given cell population under clonal conditions. The protocol begins with the seeding of the cells at a density that allows for the generation of clonal neurospheres. The neurospheres are then transferred to chambered coverslips and differentiated under clonal conditions in conditioned medium, which maximizes the differentiation potential of the neurospheres. Finally, the NSC frequency is calculated based on neurosphere formation and multipotency capabilities. Utilities of this protocol include the evaluation of candidate NSC markers, purification of NSCs, and the ability to distinguish NSCs from NPs. This method takes 13 days to perform, which is much shorter than current methods to enumerate NSC frequency.
神经干细胞(NSCs)具有自我更新能力,并能分化产生三种主要的神经谱系——星形胶质细胞、神经元和少突胶质细胞。神经干细胞和神经祖细胞(NPs)通常在体外培养成神经球。本方案详细描述了如何在克隆条件下确定给定细胞群体中的神经干细胞频率。该方案首先以允许产生克隆神经球的密度接种细胞。然后将神经球转移到有腔盖玻片上,并在条件培养基中在克隆条件下进行分化,这可使神经球的分化潜能最大化。最后,根据神经球形成和多能性能力计算神经干细胞频率。本方案的用途包括评估候选神经干细胞标志物、纯化神经干细胞以及区分神经干细胞和神经祖细胞的能力。该方法执行需要13天,比目前计算神经干细胞频率的方法所需时间短得多。