Rushing Gabrielle, Ihrie Rebecca A
Program in Neuroscience, Vanderbilt University, Nashville, TN 37232, USA.
Departments of Cancer Biology and Neurological Surgery, Vanderbilt University, Nashville, TN 37232, USA.
Front Biol (Beijing). 2016 Aug;11(4):261-284. doi: 10.1007/s11515-016-1407-1. Epub 2016 Jul 8.
The origin and classification of neural stem cells (NSCs) has been a subject of intense investigation for the past two decades. Efforts to categorize NSCs based on their location, function and expression have established that these cells are a heterogeneous pool in both the embryonic and adult brain. The discovery and additional characterization of adult NSCs has introduced the possibility of using these cells as a source for neuronal and glial replacement following injury or disease. To understand how one could manipulate NSC developmental programs for therapeutic use, additional work is needed to elucidate how NSCs are programmed and how signals during development are interpreted to determine cell fate.
This review describes the identification, classification and characterization of NSCs within the large neurogenic niche of the ventricular-subventricular zone (V-SVZ).
A literature search was conducted using Pubmed including the keywords "ventricular-subventricular zone," "neural stem cell," "heterogeneity," "identity" and/or "single cell" to find relevant manuscripts to include within the review. A special focus was placed on more recent findings using single-cell level analyses on neural stem cells within their niche(s).
This review discusses over 20 research articles detailing findings on V-SVZ NSC heterogeneity, over 25 articles describing fate determinants of NSCs, and focuses on 8 recent publications using distinct single-cell analyses of neural stem cells including flow cytometry and RNA-seq. Additionally, over 60 manuscripts highlighting the markers expressed on cells within the NSC lineage are included in a chart divided by cell type.
Investigation of NSC heterogeneity and fate decisions is ongoing. Thus far, much research has been conducted in mice however, findings in human and other mammalian species are also discussed here. Implications of NSC heterogeneity established in the embryo for the properties of NSCs in the adult brain are explored, including how these cells may be redirected after injury or genetic manipulation.
在过去二十年中,神经干细胞(NSCs)的起源和分类一直是深入研究的课题。基于其位置、功能和表达对神经干细胞进行分类的研究表明,这些细胞在胚胎和成体大脑中都是一个异质性群体。成体神经干细胞的发现及进一步表征为损伤或疾病后将这些细胞用作神经元和神经胶质细胞替代来源带来了可能性。为了理解如何操纵神经干细胞的发育程序用于治疗,需要开展更多工作来阐明神经干细胞是如何被编程的,以及发育过程中的信号是如何被解读以决定细胞命运的。
本综述描述了脑室下区(V-SVZ)这个大神经生发微环境中神经干细胞的鉴定、分类和表征。
使用PubMed进行文献检索,关键词包括“脑室下区”、“神经干细胞”、“异质性”、“特性”和/或“单细胞”,以查找相关手稿纳入本综述。特别关注了对神经干细胞微环境内神经干细胞进行单细胞水平分析的最新研究结果。
本综述讨论了20多篇详细阐述V-SVZ神经干细胞异质性研究结果的科研文章,25多篇描述神经干细胞命运决定因素的文章,并重点关注了8篇近期使用包括流式细胞术和RNA测序在内的不同神经干细胞单细胞分析的出版物。此外,一个按细胞类型划分的图表中包含了60多篇强调神经干细胞谱系中细胞所表达标志物的手稿。
对神经干细胞异质性和命运决定的研究仍在进行中。到目前为止,已经在小鼠身上开展了大量研究,不过这里也讨论了在人类和其他哺乳动物物种中的研究结果。探讨了胚胎中建立的神经干细胞异质性对成体大脑中神经干细胞特性的影响,包括这些细胞在损伤或基因操作后如何被重新定向。