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The Dentate Gyrus Grows Throughout Life Despite Turnover of Developmentally-Born Neurons.

Overview

Authors: Tina Ciric1,2, Shaina P. Cahill1,2, Tyler Lin1,2, Si‐ah Choi1,2, Jason S. Snyder1,2
ORCID iDs: Jason S. Snyder
  1. Department of Psychology University of British Columbia Vancouver Canada
  2. Djavad Mowafaghian Center for Brain Health University of British Columbia Vancouver Canada
Journal: Hippocampus, volume 36, issue 3, article e70099
Dates: received 18 February 2026; accepted 10 April 2026; published online 19 April 2026; in print May 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1002/hipo.70099 · PMID 42002876 · PMCID PMC13092647 · OpenAlex W7154916021
Open access: hybrid, a free copy (OpenAlex)
Status: empty repository
Categories: rat (organism), developmental (subfield)
Methods: Statistics
MeSH: Aging*, Dentate Gyrus*, Neurogenesis*, Neurons*, Animals, Cell Count, Cell Proliferation, Ki-67 Antigen, Male, Neurodevelopment, Rats (* major topic)
Topic: Neurogenesis and neuroplasticity mechanisms (Developmental Neuroscience, Neuroscience), according to OpenAlex
Citations: not cited yet (Europe PMC); 63 references in the paper

Abstract

Adult‐born hippocampal neurons are highly plastic but there remains uncertainty about the magnitude of neurogenesis and its long‐term functional consequences. Theoretical predictions indicate that adult neurogenesis should lead to substantial growth of the dentate gyrus (DG) granule cell population. However, in practice, most studies find no changes in total cell number across adulthood. This discrepancy may partly be a sensitivity issue, where small sample sizes and the examination of older age windows (when neurogenesis is reduced) have prevented detection. However, neurogenic growth could also be masked by the turnover of developmentally‐born DG neurons, which are known to die off in normal aging. To address the question of how neuronal birth and loss impacts DG population dynamics, here we quantified numbers of developmentally‐born neurons, proliferating Ki67+ cells (as a proxy for adult‐born neurons), and total DG neurons from 2–18 months of age in the rat. We estimate that over this timeframe 670,000 adult‐born neurons are added (30% of the total population). Consistent with neurogenic growth, the total number of DG neurons increased across adulthood. However, net growth was only 385,000 cells, which is less than predicted by adult neurogenesis alone. Indeed, 20% of developmentally‐born neurons were lost over the same interval, and so we propose that the difference is explained by neuronal turnover. Neuronal persistence and turnover may be relevant for theories of hippocampal long‐term memory, as well as for understanding psychiatric conditions that are characterized by hippocampal plasticity and atrophy.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

No file of the authors' code could be read here: it is described below, and read at its source.

figshare 19319849

License: CC-BY-4.0
State: the link answers, verified on 28 September 2026
Evidence: files inventoried
Size: 2 files, 0 scripts
Software Heritage: not checked
Found in: the references
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 28 September 2026: the link answers (HTTP 200)
  • 28 September 2026: the link answers (HTTP 200)

Tracing map

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  • 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 0 scripts, each with its path and the digest of its content;
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Data

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Data Availability Statement

The data that supports the findings of this study are available in the Supporting Information of this article.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

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Version 2, 28 September 2026

  • Publisher: n/a → Wiley

Version 1, 28 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 5 authors, 11 MeSH terms, 3 funders, 61 references.

Cite

This paper

Ciric, T., Cahill, S. P., Lin, T., Choi, S., & Snyder, J. S. (2026). The Dentate Gyrus Grows Throughout Life Despite Turnover of Developmentally-Born Neurons. Hippocampus, 36(3), e70099. https://doi.org/10.1002/hipo.70099

BibTeX

@article{ciric2026dentate,
author = {Ciric, Tina and Cahill, Shaina P. and Lin, Tyler and Choi, Si‐ah and Snyder, Jason S.},
title = {{The Dentate Gyrus Grows Throughout Life Despite Turnover of Developmentally-Born Neurons}},
journal = {Hippocampus},
year = {2026},
month = may,
volume = {36},
number = {3},
pages = {e70099},
publisher = {Wiley},
issn = {1050-9631},
doi = {10.1002/hipo.70099},
url = {https://doi.org/10.1002/hipo.70099},
pmid = {42002876},
pmcid = {PMC13092647}
}

RIS

TY - JOUR
AU - Ciric, Tina
AU - Cahill, Shaina P.
AU - Lin, Tyler
AU - Choi, Si‐ah
AU - Snyder, Jason S.
TI - The Dentate Gyrus Grows Throughout Life Despite Turnover of Developmentally-Born Neurons
T2 - Hippocampus
J2 - Hippocampus
PY - 2026
DA - 2026/05/01
VL - 36
IS - 3
SP - e70099
SN - 1050-9631
PB - Wiley
DO - 10.1002/hipo.70099
UR - https://doi.org/10.1002/hipo.70099
LA - en
ER -

CSL-JSON

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