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Neurogenesis and Regeneration of Nervous Tissue01:15

Neurogenesis and Regeneration of Nervous Tissue

In the CNS, neurogenesis, the birth of new neurons from stem cells, is limited to the hippocampus in adults. In other regions of the brain and spinal cord, neurogenesis is almost non-existent due to inhibitory influences from neuroglia, especially oligodendrocytes, and the absence of growth-stimulating cues. The myelin produced by oligodendrocytes in the CNS inhibits neuronal regeneration. Furthermore, astrocytes proliferate rapidly after neuronal damage, forming scar tissue that physically...
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Related Experiment Video

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Fluorescence and Bioluminescence Imaging of Subcellular Ca2+ in Aged Hippocampal Neurons
13:24

Fluorescence and Bioluminescence Imaging of Subcellular Ca2+ in Aged Hippocampal Neurons

Published on: December 1, 2015

New neurons in an aged brain.

Star W Lee1, Gregory D Clemenson, Fred H Gage

  • 1Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.

Behavioural Brain Research
|October 26, 2011
PubMed
Summary
This summary is machine-generated.

Aging significantly reduces adult hippocampal neurogenesis, impacting neural progenitor cells and the neurogenic niche. This decline may affect cognitive function, necessitating new research approaches.

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Area of Science:

  • Neuroscience
  • Cell Biology
  • Aging Research

Background:

  • Adult hippocampal neurogenesis is a continuous process throughout life, crucial for synaptic plasticity.
  • Neurogenesis rate declines with age, marked by reduced progenitor cell proliferation, differentiation, and survival.
  • Age-related intrinsic changes in neural progenitor cells and the neurogenic niche microenvironment contribute to this decline.

Purpose of the Study:

  • To review age-related changes in adult hippocampal neurogenesis.
  • To discuss alterations in neural progenitor cells and the neurogenic niche in aging.
  • To examine the link between neurogenesis and cognitive function in aged animals and highlight the need for specific behavioral tasks.

Main Methods:

  • Review of existing literature on adult hippocampal neurogenesis and aging.
  • Analysis of studies on intrinsic properties of neural progenitor cells (gene transcription, telomerase activity).
  • Examination of age-related changes in neurogenic niche cells (astrocytes, microglia, endothelial cells).
  • Discussion of behavioral paradigms for assessing hippocampus-dependent cognition.

Main Results:

  • Older animals exhibit significantly reduced neurogenesis compared to younger ones.
  • Intrinsic cellular properties and niche cell alterations contribute to age-related neurogenesis decline.
  • Correlation between decreased neurogenesis and cognitive impairment is common, but not universal, in aged mice.

Conclusions:

  • Aging profoundly impacts adult hippocampal neurogenesis through cellular and environmental changes.
  • The neurogenic niche undergoes significant age-related alterations affecting neural progenitor cell function.
  • Further development of neurogenesis-dependent behavioral tasks is crucial for understanding cognitive aging.