Chaker Zayna, Codega Paolo, Doetsch Fiona
Biozentrum, University of Basel, Basel, Switzerland.
Department of Pathology and Cell Biology, Columbia University, New York, NY, USA.
Wiley Interdiscip Rev Dev Biol. 2016 Nov;5(6):640-658. doi: 10.1002/wdev.248. Epub 2016 Sep 20.
Neural stem cells (NSCs) reside in specialized niches in the adult mammalian brain. The ventricular-subventricular zone (V-SVZ), adjacent to the lateral ventricles, gives rise to olfactory bulb (OB) neurons, and some astrocytes and oligodendrocytes throughout life. In vitro assays have been widely used to retrospectively identify NSCs. However, cells that behave as stem cells in vitro do not reflect the identity, diversity, and behavior of NSCs in vivo. Novel tools including fluorescence activated cell sorting, lineage-tracing, and clonal analysis have uncovered multiple layers of adult V-SVZ NSC heterogeneity, including proliferation state and regional identity. In light of these findings, we reexamine the concept of adult NSCs, considering heterogeneity as a key parameter for analyzing their dynamics in vivo. V-SVZ NSCs form a mosaic of quiescent (qNSCs) and activated cells (aNSCs) that reside in regionally distinct microdomains, reflecting their regional embryonic origins, and give rise to specific subtypes of OB interneurons. Prospective purification and transcriptome analysis of qNSCs and aNSCs has illuminated their molecular and functional properties. qNSCs are slowly dividing, have slow kinetics of neurogenesis in vivo, can be recruited to regenerate the V-SVZ, and only rarely give rise to in vitro colonies. aNSCs are highly proliferative, undergo rapid clonal expansion of the neurogenic lineage in vivo, and readily form in vitro colonies. Key open questions remain about stem cell dynamics in vivo and the lineage relationship between qNSCs and aNSCs under homeostasis and regeneration, as well as context-dependent plasticity of regionally distinct adult NSCs under different external stimuli. WIREs Dev Biol 2016, 5:640-658. doi: 10.1002/wdev.248 For further resources related to this article, please visit the WIREs website.
神经干细胞(NSCs)存在于成年哺乳动物大脑的特定微环境中。与侧脑室相邻的脑室下区(V-SVZ)终生都能产生嗅球(OB)神经元以及一些星形胶质细胞和少突胶质细胞。体外实验已被广泛用于追溯性鉴定神经干细胞。然而,在体外表现为干细胞的细胞并不能反映神经干细胞在体内的特性、多样性和行为。包括荧光激活细胞分选、谱系追踪和克隆分析在内的新型工具揭示了成年V-SVZ神经干细胞异质性的多个层面,包括增殖状态和区域特性。鉴于这些发现,我们重新审视成年神经干细胞的概念,将异质性视为分析其体内动态的关键参数。V-SVZ神经干细胞形成了一个由静止(qNSCs)和激活细胞(aNSCs)组成的镶嵌体,它们位于区域不同的微域中,反映了它们的区域胚胎起源,并产生OB中间神经元的特定亚型。对qNSCs和aNSCs的前瞻性纯化和转录组分析揭示了它们的分子和功能特性。qNSCs分裂缓慢,在体内神经发生动力学缓慢,可被募集以再生V-SVZ,并且很少产生体外集落。aNSCs具有高度增殖性,在体内经历神经源性谱系的快速克隆扩增,并易于形成体外集落。关于体内干细胞动态以及在稳态和再生条件下qNSCs和aNSCs之间的谱系关系,以及不同外部刺激下区域不同的成年神经干细胞的背景依赖性可塑性,仍然存在关键的开放性问题。WIREs发育生物学2016年,5:640 - 658。doi:10.1002/wdev.248 有关本文的更多资源,请访问WIREs网站。