Abstract

Newborn neurons in the subgranular zone (SGZ) of the hippocampus incorporate into the dentate gyrus and mature. Numerous studies have focused on hippocampal neurogenesis because of its importance in learning and memory. However, it is largely unknown whether hippocampal neurogenesis is involved in memory extinction per se. Here, we sought to examine the possibility that hippocampal neurogenesis may play a critical role in the formation and extinction of hippocampus-dependent contextual fear memory. By methylazoxymethanol acetate (MAM) or gamma-ray irradiation, hippocampal neurogenesis was impaired in adult mice. Under our experimental conditions, only a severe impairment of hippocampal neurogenesis inhibited the formation of contextual fear memory. However, the extinction of contextual fear memory was not affected. These results suggest that although adult newborn neurons contribute to contextual fear memory, they may not be involved in the extinction or erasure of hippocampus-dependent contextual fear memory.

Highlights

  • Newborn neurons continuously incorporate into neuronal circuits during development

  • Since newborn neurons show a high capacity of synaptic plasticity and incorporate into preexisting circuits, it is conceivable that adult neurogenesis may contribute to building up or impairing the circuitry for memory storage [21,22]

  • We examined the effect of hippocampal neurogenesis on the formation and extinction of a hippocampus-dependent contextual fear memory

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Summary

Introduction

Newborn neurons continuously incorporate into neuronal circuits during development. In the adult brain, neurogenesis occurs in the subgranular zone (SGZ) of the hippocampus and the subventricular zone (SVZ) of the lateral ventricle [1]. Generated neurons in the SVZ migrate to the olfactory bulb and play key roles in olfactory memory [2]. In the SGZ region, newly generated cells are differentiated into both neurons and glial cells, and the newborn neurons incorporate to the granule cell layer of the dentate gyrus [2]. A growing body of evidence supports the contribution of hippocampal newborn neurons to hippocampus-dependent memories [3,4,5]. Ablated neurogenesis impaired contextual fear conditioning, but did not impair cued fear conditioning, which is independent of the hippocampus [3,5].

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