Department of Psychology, Program in Neuroscience, Brain Research Centre, University of British Columbia Vancouver, BC, Canada.
Front Neurosci. 2013 Apr 16;7:57. doi: 10.3389/fnins.2013.00057. eCollection 2013.
The structure of the mammalian hippocampus continues to be modified throughout life by continuous addition of neurons in the dentate gyrus. Although the existence of adult neurogenesis is now widely accepted the function that adult generated granule cells play is a topic of intense debate. Many studies have argued that adult generated neurons, due to unique physiological characteristics, play a unique role in hippocampus-dependent learning and memory. However, it is not currently clear whether this is the case or what specific capability adult generated neurons may confer that developmentally generated neurons do not. These questions have been addressed in numerous ways, from examining the effects of increasing or decreasing neurogenesis to computational modeling. One particular area of research has examined the effects of hippocampus dependent learning on proliferation, survival, integration and activation of immature neurons in response to memory retrieval. Within this subfield there remains a range of data showing that hippocampus dependent learning may increase, decrease or alternatively may not alter these components of neurogenesis in the hippocampus. Determining how and when hippocampus-dependent learning alters adult neurogenesis will help to further clarify the role of adult generated neurons. There are many variables (such as age of immature neurons, species, strain, sex, stress, task difficulty, and type of learning) as well as numerous methodological differences (such as marker type, quantification techniques, apparatus size etc.) that could all be crucial for a clear understanding of the interaction between learning and neurogenesis. Here, we review these findings and discuss the different conditions under which hippocampus-dependent learning impacts adult neurogenesis in the dentate gyrus.
哺乳动物海马体的结构在其一生中通过齿状回中新神经元的持续添加而不断改变。尽管成年神经发生的存在现在已被广泛接受,但成年产生的颗粒细胞的功能仍是一个激烈争论的话题。许多研究认为,由于独特的生理特征,成年产生的神经元在海马体依赖的学习和记忆中发挥着独特的作用。然而,目前尚不清楚情况是否如此,或者成年产生的神经元可能赋予哪些特定的能力,而发育产生的神经元则没有。这些问题已经通过多种方式得到了解决,从检查增加或减少神经发生的影响到计算建模。一个特别的研究领域研究了海马体依赖的学习对增殖、存活、整合和激活记忆检索中不成熟神经元的影响。在这个子领域内,仍有一系列数据表明,海马体依赖的学习可能会增加、减少或不会改变海马体中的这些神经发生成分。确定海马体依赖的学习如何以及何时改变成年神经发生将有助于进一步阐明成年产生的神经元的作用。有许多变量(如不成熟神经元的年龄、物种、品系、性别、应激、任务难度和学习类型)以及许多方法学差异(如标记类型、定量技术、仪器大小等),这些对于清楚地理解学习和神经发生之间的相互作用都至关重要。在这里,我们回顾了这些发现,并讨论了在不同条件下,海马体依赖的学习如何影响齿状回中的成年神经发生。