Cited by 493Neurogenesis and neuroplasticity mechanismsMemory and Neural MechanismsNeuroscience and Neuropharmacology Research

Adult-Born Hippocampal Dentate Granule Cells Undergoing Maturation Modulate Learning and Memory in the Brain

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Deng, Wei, Saxe, Michael D., Gallina, Iryna S., Gage, Fred H.·2009·The Journal of Neuroscience

Abstract

Adult-born dentate granule cells (DGCs) contribute to learning and memory, yet it remains unknown when adult-born DGCs become involved in the cognitive processes. During neurogenesis, immature DGCs display distinctive physiological characteristics while undergoing morphological maturation before final integration into the neural circuits. The survival and activity of the adult-born DGCs can be influenced by the experience of the animal during a critical period when newborn DGCs are still immature. To assess the temporal importance of adult neurogenesis, we developed a transgenic mouse model that allowed us to transiently reduce the numbers of adult-born DGCs in a temporally regulatable manner. We found that mice with a reduced population of adult-born DGCs at the immature stage were deficient in forming robust, long-term spatial memory and displayed impaired performance in extinction tasks. These results suggest that immature DGCs that undergo maturation make important contributions to learning and memory.

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Authors
Deng, W., Saxe, M. D., Gallina, I. S., & Gage, F. H.
Affiliations
Salk Institute for Biological Studies (US)
Venue
The Journal of Neuroscience
Published
2009-10-28
Volume
29
Issue
43
Pages
13532-13542
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2075257572
Cited by
493
References
3
Citations by year
2026: 7 · 2025: 19 · 2024: 16 · 2023: 11 · 2022: 10 · 2021: 28 · 2020: 23 · 2019: 19 · 2018: 27 · 2017: 37 · 2016: 36 · 2015: 46 · 2014: 39 · 2013: 47 · 2012: 34
FWCI
13.39
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • James S. McDonnell Foundation
  • National Institutes of Health (NS-05050217)
  • National Institute on Aging (AG 020938, R01AG020938)
  • National Institute of Neurological Disorders and Stroke (R01NS052842, R01NS050217, NS-05052842, NS 05050217)
Topics
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords
adult neurogenesis, dentate gyrus granule cells, hippocampus, neuronal maturation, spatial memory, learning, memory extinction, transgenic mouse model, critical period, long-term memory formation
MeSH terms
Animals, Brain, Conditioning, Classical, Extinction, Psychological, Fear, Female, Intermediate Filament Proteins, Learning, Male, Memory, Mice, Inbred C57BL, Mice, Transgenic, Nerve Tissue Proteins, Neurons, Neuropsychological Tests, Space Perception, Time Factors, Maze Learning, Dentate Gyrus, Mice, Adult Stem Cells, Nestin

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