Maric Dragan, Barker Jeffery L
National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Curr Protoc Neurosci. 2005 Nov;Chapter 3:Unit 3.18. doi: 10.1002/0471142301.ns0318s33.
Neural stem cells (NSCs) are defined as undifferentiated cells originating from the neuroectoderm that have the capacity both to perpetually self-renew without differentiating and to generate multiple types of lineage-restricted progenitors (LRPs). LRPs can themselves undergo limited self-renewal and ultimately differentiate into highly specialized cells that make up the nervous system. However, this physiologically delimited definition of NSCs and LRPs has become increasingly blurred due to lack of protocols for effectively separating these types of cells from primary tissues. This unit discusses recent attempts using fluorescence-activated cell sorting (FACS) strategies to prospectively isolate NSCs from different types of LRPs as they appear in vivo, and details a protocol that optimally attains this goal. Thus, the strategy presented here provides a framework for more precise studies of NSC and LRP cell biology in the future, which can be applied to all vertebrates, including humans.
神经干细胞(NSCs)被定义为起源于神经外胚层的未分化细胞,它们具有既能不分化地持续自我更新,又能产生多种谱系受限祖细胞(LRPs)的能力。LRPs自身可以进行有限的自我更新,并最终分化为构成神经系统的高度特化细胞。然而,由于缺乏从原代组织中有效分离这些细胞类型的方案,NSCs和LRPs这种生理学上界定的定义变得越来越模糊。本单元讨论了最近使用荧光激活细胞分选(FACS)策略在体内出现时从不同类型的LRPs中前瞻性分离NSCs的尝试,并详细介绍了一个能最佳实现这一目标的方案。因此,这里提出的策略为未来更精确地研究NSC和LRP细胞生物学提供了一个框架,该框架可应用于包括人类在内的所有脊椎动物。