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Updated: Feb 12, 2026

Immunohistochemistry and Multiple Labeling with Antibodies from the Same Host Species to Study Adult Hippocampal Neurogenesis
Published on: April 22, 2015
Human Hippocampal Neurogenesis Persists throughout Aging.
Maura Boldrini1, Camille A Fulmore2, Alexandria N Tartt2
1Department of Psychiatry, Columbia University, New York, NY 10032, USA; Division of Molecular Imaging and Neuropathology, NYS Psychiatric Institute, New York, NY 10032, USA.
Healthy aging preserves adult hippocampal neurogenesis in humans, contrary to expectations. While neuroplasticity and angiogenesis decrease, the dentate gyrus volume and neuron numbers remain stable, suggesting sustained cognitive function.
Area of Science:
- Neuroscience
- Aging Research
- Human Anatomy
Background:
- Adult hippocampal neurogenesis is known to decline with age in many species.
- Human aging is hypothesized to involve reduced neurogenesis and angiogenesis, impacting the dentate gyrus (DG).
- Concurrent changes in these hippocampal parameters during human aging are not well understood.
Purpose of the Study:
- To investigate age-related changes in adult neurogenesis, neuroplasticity, angiogenesis, and hippocampal volume in healthy humans.
- To determine if neurogenesis is preserved in the aging human hippocampus.
Main Methods:
- Analysis of autopsy-derived hippocampi from healthy individuals aged 14 to 79.
- Quantification of neural progenitors, immature neurons, glia, and mature granule neurons.
- Assessment of dentate gyrus (DG) volume, angiogenesis, and progenitor pool status.
Main Results:
- No significant age-related differences were found in the number of intermediate neural progenitors, immature neurons, glia, mature granule neurons, or DG volume.
- Older individuals showed reduced angiogenesis and neuroplasticity, particularly in the anterior-mid DG.
- A smaller quiescent progenitor pool was observed in the anterior-mid DG of older subjects, with no changes in the posterior DG.
Conclusions:
- Healthy aging in humans is associated with preserved hippocampal neurogenesis, including the number of immature neurons and overall DG volume.
- Despite preserved neurogenesis, declines in angiogenesis and neuroplasticity occur with age, localized to specific DG regions.
- Sustained neurogenesis may support lifelong cognitive function, while age-related declines in plasticity could impact cognitive-emotional resilience.
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