Neural Regeneration Laboratory, Department of Anatomy and Neuroscience, Centre for Neuroscience Research, The University of Melbourne Parkville, VIC, Australia.
Front Cell Neurosci. 2013 Jan 18;6:70. doi: 10.3389/fncel.2012.00070. eCollection 2012.
Neural stem/precursor cells in the adult brain reside in the subventricular zone (SVZ) of the lateral ventricles and the subgranular zone (SGZ) of the dentate gyrus in the hippocampus. These cells primarily generate neuroblasts that normally migrate to the olfactory bulb (OB) and the dentate granule cell layer respectively. Following brain damage, such as traumatic brain injury, ischemic stroke or in degenerative disease models, neural precursor cells from the SVZ in particular, can migrate from their normal route along the rostral migratory stream (RMS) to the site of neural damage. This neural precursor cell response to neural damage is mediated by release of endogenous factors, including cytokines and chemokines produced by the inflammatory response at the injury site, and by the production of growth and neurotrophic factors. Endogenous hippocampal neurogenesis is frequently also directly or indirectly affected by neural damage. Administration of a variety of factors that regulate different aspects of neural stem/precursor biology often leads to improved functional motor and/or behavioral outcomes. Such factors can target neural stem/precursor proliferation, survival, migration and differentiation into appropriate neuronal or glial lineages. Newborn cells also need to subsequently survive and functionally integrate into extant neural circuitry, which may be the major bottleneck to the current therapeutic potential of neural stem/precursor cells. This review will cover the effects of a range of intrinsic and extrinsic factors that regulate neural stem/precursor cell functions. In particular it focuses on factors that may be harnessed to enhance the endogenous neural stem/precursor cell response to neural damage, highlighting those that have already shown evidence of preclinical effectiveness and discussing others that warrant further preclinical investigation.
成年大脑中的神经干细胞/前体细胞位于侧脑室的室下区 (SVZ) 和海马齿状回的颗粒下区 (SGZ)。这些细胞主要产生神经母细胞,它们通常分别迁移到嗅球 (OB) 和齿状回颗粒细胞层。在脑损伤后,例如创伤性脑损伤、缺血性中风或退行性疾病模型中,特别是来自 SVZ 的神经前体细胞,可以从它们沿着前脑侧脑室迁移流 (RMS) 的正常途径迁移到神经损伤部位。这种神经前体细胞对神经损伤的反应是由内源性因子介导的,包括损伤部位炎症反应产生的细胞因子和趋化因子,以及生长和神经营养因子的产生。内源性海马神经发生也经常直接或间接地受到神经损伤的影响。内源性海马神经发生也经常直接或间接地受到神经损伤的影响。给予各种调节神经干细胞/前体细胞生物学不同方面的因子通常会导致改善的运动和/或行为功能结果。这些因子可以靶向神经干细胞/前体细胞的增殖、存活、迁移和分化为适当的神经元或神经胶质谱系。新生细胞还需要随后存活并功能性地整合到现存的神经回路中,这可能是神经干细胞/前体细胞当前治疗潜力的主要瓶颈。本综述将涵盖一系列调节神经干细胞/前体细胞功能的内在和外在因素的影响。特别是,它侧重于可以利用来增强内源性神经干细胞/前体细胞对神经损伤的反应的因子,强调那些已经显示出临床前有效性证据的因子,并讨论其他值得进一步临床前研究的因子。