Department of Biology, Brain and Mind Research Institute, University of Ottawa, Ontario, Canada; Australian Regenerative Medicine Institute, Monash University Clayton Campus, Clayton, VIC, Australia.
Department of Cell and Systems Biology, University of Toronto, Ontario, M5S 3G5, Canada.
Prog Neurobiol. 2018 Nov;170:99-114. doi: 10.1016/j.pneurobio.2018.06.004. Epub 2018 Jun 11.
Neural stem and progenitor cells (NSPCs) are the primary source of new neurons in the brain and serve critical roles in tissue homeostasis and plasticity throughout life. Within the vertebrate brain, NSPCs are located within distinct neurogenic niches differing in their location, cellular composition, and proliferative behaviour. Heterogeneity in the NSPC population is hypothesized to reflect varying capacities for neurogenesis, plasticity and repair between different neurogenic zones. Since the discovery of adult neurogenesis, studies have predominantly focused on the behaviour and biological significance of adult NSPCs (aNSPCs) in rodents. However, compared to rodents, who show lifelong neurogenesis in only two restricted neurogenic niches, zebrafish exhibit constitutive neurogenesis across multiple stem cell niches that provide new neurons to every major brain division. Accordingly, zebrafish are a powerful model to probe the unique cellular and molecular profiles of NSPCs and investigate how these profiles govern tissue homeostasis and regenerative plasticity within distinct stem cell populations over time. Amongst the NSPC populations residing in the zebrafish central nervous system (CNS), proliferating radial-glia, quiescent radial-glia and neuro-epithelial-like cells comprise the majority. Here, we provide insight into the extent to which these distinct NSPC populations function and mature during development, respond to experience, and contribute to successful CNS regeneration in teleost fish. Together, our review brings to light the dynamic biological roles of these individual NSPC populations and showcases their diverse regenerative modes to achieve vertebrate brain repair later in life.
神经干细胞和祖细胞(NSPCs)是大脑中新神经元的主要来源,在整个生命过程中发挥着组织内稳态和可塑性的关键作用。在脊椎动物大脑中,NSPCs 位于不同的神经发生龛位,其位置、细胞组成和增殖行为不同。NSPC 群体的异质性被假设反映了不同神经发生区之间的神经发生、可塑性和修复能力的差异。自成年神经发生发现以来,研究主要集中在啮齿动物中成年 NSPCs(aNSPCs)的行为和生物学意义上。然而,与在两个有限的神经发生龛位中表现出终生神经发生的啮齿动物相比,斑马鱼在多个干细胞龛位中表现出组成性神经发生,为每个主要脑区提供新的神经元。因此,斑马鱼是一种强大的模型,可以探究 NSPCs 的独特细胞和分子特征,并研究这些特征如何随时间在不同的干细胞群体中调节组织内稳态和再生可塑性。在斑马鱼中枢神经系统(CNS)中存在的 NSPC 群体中,增殖的放射状胶质细胞、静止的放射状胶质细胞和神经上皮样细胞占大多数。在这里,我们深入了解这些不同的 NSPC 群体在发育过程中、对经验的反应以及在硬骨鱼类成功的中枢神经系统再生中发挥功能和成熟的程度。总的来说,我们的综述揭示了这些单个 NSPC 群体的动态生物学作用,并展示了它们的不同再生模式,以实现成年后的脊椎动物大脑修复。