Evidence map›Paper›PMID 26179319›Full record

ReviewThe Journal of comparative neurology2016

Evolution of the mammalian dentate gyrus.

Robert F Hevner

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of comparative neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 84 citations in OpenAlex.

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  9. Clade-specific forebrain cytoarchitectures of the extinct Tasmanian tiger.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Molecular biology of serotonergic systems in avian brains.Frontiers in molecular neuroscience · 2023
    Review
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  15. What Is Adult Hippocampal Neurogenesis Good for?Frontiers in neuroscience · 2022
    Article
  16. Review
  17. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Robert F HevnerCenter for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, 98101.
Neurological Surgery · US

Funding

Intermediate Progenitor Cells in Adult Hippocampal NeurogenesisR01MH080766 · NIMH · SEATTLE CHILDREN'S HOSPITAL · PI HEVNER, ROBERT F · 2008 to 2012
$2.6M
Intermediate neuronal progenitors in neocortical developmentR01NS085081 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI HEVNER, ROBERT F · 2013 to 2017
$2.1M
Development and Malformations of the Dentate GyrusR01NS092339 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HEVNER, ROBERT F · 2016 to 2020
$1.9M
Delta-Notch Signaling by Intermediate Neuronal Progenitors: Live ImagingR21MH087070 · NIMH · SEATTLE CHILDREN'S HOSPITAL · PI HEVNER, ROBERT F · 2009 to 2010
$536k
NIMH NIH HHS R01 MH080766NIMH NIH HHS R01MH080766NIMH NIH HHS R21 MH087070NIMH NIH HHS R21MH087070NINDS NIH HHS R01 NS085081NINDS NIH HHS R01NS085081NINDS NIH HHS R01 NS092339
6 · The paper itself

Abstract

The dentate gyrus (DG), a part of the hippocampal formation, has important functions in learning, memory, and adult neurogenesis. Compared with homologous areas in sauropsids (birds and reptiles), the mammalian DG is larger and exhibits qualitatively different phenotypes: 1) folded (C- or V-shaped) granule neuron layer, concave toward the hilus and delimited by a hippocampal fissure; 2) nonperiventricular adult neurogenesis; and 3) prolonged ontogeny, involving extensive abventricular (basal) migration and proliferation of neural stem and progenitor cells (NSPCs). Although gaps remain, available data indicate that these DG traits are present in all orders of mammals, including monotremes and marsupials. The exception is Cetacea (whales, dolphins, and porpoises), in which DG size, convolution, and adult neurogenesis have undergone evolutionary regression. Parsimony suggests that increased growth and convolution of the DG arose in stem mammals concurrently with nonperiventricular adult hippocampal neurogenesis and basal migration of NSPCs during development. These traits could all result from an evolutionary change that enhanced radial migration of NSPCs out of the periventricular zones, possibly by epithelial-mesenchymal transition, to colonize and maintain nonperiventricular proliferative niches. In turn, increased NSPC migration and clonal expansion might be a consequence of growth in the cortical hem (medial patterning center), which produces morphogens such as Wnt3a, generates Cajal-Retzius neurons, and is regulated by Lhx2. Finally, correlations between DG convolution and neocortical gyrification (or capacity for gyrification) suggest that enhanced abventricular migration and proliferation of NSPCs played a transformative role in growth and folding of neocortex as well as archicortex.

Indexed as

Biological EvolutionDentate GyrusMammalsAnimalsNeural PathwaysNeurogenesisNeurons

Identifiers

PMID26179319
PMCPMC4706817
OpenAlexW1892914051

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.