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通过成体神经发生实现齿状回的经验特异性功能修饰:未成熟阶段的关键时期。

Experience-specific functional modification of the dentate gyrus through adult neurogenesis: a critical period during an immature stage.

作者信息

Tashiro Ayumu, Makino Hiroshi, Gage Fred H

机构信息

Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.

出版信息

J Neurosci. 2007 Mar 21;27(12):3252-9. doi: 10.1523/JNEUROSCI.4941-06.2007.


DOI:10.1523/JNEUROSCI.4941-06.2007
PMID:17376985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6672473/
Abstract

Neural circuits in the dentate gyrus are continuously modified by adult neurogenesis, whose level is affected by the animal's experience. However, it is not known whether this experience-dependent anatomical modification alters the functional properties of the dentate gyrus. Here, using the expression of immediate early gene products, c-fos and Zif268, as indicators of recently activated neurons, we show that previous exposure to an enriched environment increases the total number of new neurons and the number of new neurons responding to reexposure to the same environment. The increase in the density of activated new neurons occurred specifically in response to exposure to the same environment but not to a different experience. Furthermore, we found that these experience-specific modifications are affected exclusively by previous exposure around the second week after neuronal birth but not later than 3 weeks. Thus, the animal's experience within a critical period during an immature stage of new neurons determines the survival and population response of the new neurons and may affect later neural representation of the experience in the dentate gyrus. This experience-specific functional modification through adult neurogenesis could be a mechanism by which new neurons exert a long-term influence on the function of the dentate gyrus related to learning and memory.

摘要

齿状回中的神经回路会因成体神经发生而持续改变,而成体神经发生的水平受动物经历的影响。然而,尚不清楚这种依赖于经历的解剖学改变是否会改变齿状回的功能特性。在此,我们以即刻早期基因产物c-fos和Zif268的表达作为近期被激活神经元的指标,结果表明,先前暴露于丰富环境中会增加新神经元的总数以及对再次暴露于相同环境做出反应的新神经元数量。激活的新神经元密度增加是对暴露于相同环境的特异性反应,而非对不同经历的反应。此外,我们发现这些依赖于经历的特异性改变仅受神经元出生后第二周左右的先前暴露影响,而非晚于3周。因此,动物在新神经元未成熟阶段的关键时期内的经历决定了新神经元的存活和群体反应,并可能影响随后齿状回中该经历的神经表征。这种通过成体神经发生进行的依赖于经历的特异性功能改变可能是新神经元对与学习和记忆相关的齿状回功能产生长期影响的一种机制。

相似文献

[1]
Experience-specific functional modification of the dentate gyrus through adult neurogenesis: a critical period during an immature stage.

J Neurosci. 2007-3-21

[2]
Active Dentate Granule Cells Encode Experience to Promote the Addition of Adult-Born Hippocampal Neurons.

J Neurosci. 2017-5-3

[3]
Transplanted Dentate Progenitor Cells Show Increased Survival in an Enriched Environment But Do Not Exert a Neurotrophic Effect on Spatial Memory Within 2 Weeks of Engraftment.

Cell Transplant. 2015

[4]
Strain differences in neurogenesis and activation of new neurons in the dentate gyrus in response to spatial learning.

Neuroscience. 2010-10-16

[5]
Long-term potentiation enhances neurogenesis in the adult dentate gyrus.

J Neurosci. 2006-5-31

[6]
Mastication influences the survival of newly generated cells in mouse dentate gyrus.

Neuroreport. 2005-2-28

[7]
Gonadal hormone modulation of neurogenesis in the dentate gyrus of adult male and female rodents.

Brain Res Rev. 2008-3

[8]
A behavioral task with more opportunities for memory acquisition promotes the survival of new neurons in the adult dentate gyrus.

Sci Rep. 2018-5-9

[9]
Impact of environmental enrichment on neurogenesis in the dentate gyrus during the early postnatal period.

Brain Res. 2011-8-9

[10]
Exercise enhances the proliferation of neural stem cells and neurite growth and survival of neuronal progenitor cells in dentate gyrus of middle-aged mice.

J Appl Physiol (1985). 2008-11

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[2]
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Biomolecules. 2025-4-7

[3]
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Adv Exp Med Biol. 2025

[4]
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[5]
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Front Aging Neurosci. 2024-8-2

[6]
Adult neurogenesis improves spatial information encoding in the mouse hippocampus.

Nat Commun. 2024-7-30

[7]
Modelling adult neurogenesis in the aging rodent hippocampus: a midlife crisis.

Front Neurosci. 2024-6-3

[8]
Tpr Misregulation in Hippocampal Neural Stem Cells in Mouse Models of Alzheimer's Disease.

Cells. 2023-12-1

[9]
Mitochondrial OPA1 Deficiency Is Associated to Reversible Defects in Spatial Memory Related to Adult Neurogenesis in Mice.

eNeuro. 2023-11

[10]
Early deficits in dentate circuit and behavioral pattern separation after concussive brain injury.

Exp Neurol. 2023-12

本文引用的文献

[1]
Pattern separation in the dentate gyrus and CA3 of the hippocampus.

Science. 2007-2-16

[2]
NMDA-receptor-mediated, cell-specific integration of new neurons in adult dentate gyrus.

Nature. 2006-8-24

[3]
Potential role for adult neurogenesis in the encoding of time in new memories.

Nat Neurosci. 2006-6

[4]
Hippocampal neurogenesis is not required for behavioral effects of environmental enrichment.

Nat Neurosci. 2006-6

[5]
Inhibition of neurogenesis interferes with hippocampus-dependent memory function.

Hippocampus. 2006

[6]
Distinct morphological stages of dentate granule neuron maturation in the adult mouse hippocampus.

J Neurosci. 2006-1-4

[7]
Adult-born and preexisting olfactory granule neurons undergo distinct experience-dependent modifications of their olfactory responses in vivo.

J Neurosci. 2005-11-16

[8]
Critical period plasticity in local cortical circuits.

Nat Rev Neurosci. 2005-11

[9]
A natural form of learning can increase and decrease the survival of new neurons in the dentate gyrus.

Hippocampus. 2005

[10]
Critical period for sensory experience-dependent survival of newly generated granule cells in the adult mouse olfactory bulb.

Proc Natl Acad Sci U S A. 2005-7-5

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