Evidence map›Paper›PMID 22910687›Full record

ArticlePsychoneuroendocrinology2013

Prenatal stress delays inhibitory neuron progenitor migration in the developing neocortex.

Hanna E Stevens, Tina Su, Yuchio Yanagawa, Flora M Vaccarino

Open access · greenAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 16% 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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

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1 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Hanna E StevensChild Study Center, Yale University, 230 South Frontage Rd, New Haven, CT 06520, United States. hanna.stevens@yale.edu
Tina Su
Yuchio Yanagawa
Flora M Vaccarino
Yale University · USGunma University · JP

Funding

TRAINING PROGRAM IN CHILDHOOD NEUROPSYCHIATRIC DISORDERST32MH018268 · NIMH · YALE UNIVERSITY · PI Michael H Bloch, MICHAEL J CROWLEY · 1985 to 2026
$11.0M
Schizophrenia Research FellowshipR25MH071584 · NIMH · YALE UNIVERSITY · PI Christopher John Pittenger · 2005 to 2026
$4.4M
Research Training for Medical Students & Physician-Scientists in Child PsychiatryR25MH077823 · NIMH · YALE UNIVERSITY · PI ANDRES S MARTIN · 2006 to 2026
$4.0M
Morphogenesis and Function of the Cerebral CortexR01MH067715 · NIMH · YALE UNIVERSITY · PI VACCARINO, FLORA M · 2004 to 2013
$3.8M
Prenatal stress and the development of inhibitory neurons in the forebrainK08MH086812 · NIMH · YALE UNIVERSITY · PI STEVENS, HANNA E · 2010 to 2014
$850k
NIMH NIH HHS K08 MH086812NIMH NIH HHS K08 MH086812-01NIMH NIH HHS R01 MH067715NIMH NIH HHS R25 MH071584NIMH NIH HHS R25 MH077823NIMH NIH HHS T32 MH018268
6 · The paper itself

Abstract

Prenatal stress has been widely demonstrated to have links with behavioral problems in clinical populations and animal models, however, few investigations have examined the immediate developmental events that are affected by prenatal stress. Here, we utilize GAD67GFP transgenic mice in which GABAergic progenitors express green fluorescent protein (GFP) to examine the impact of prenatal stress on the development of these precursors to inhibitory neurons. Pregnant female mice were exposed to restraint stress three times daily from embryonic day 12 (E12) onwards. Their offspring demonstrated changes in the distribution of GFP-positive (GFP+) GABAergic progenitors in the telencephalon as early as E13 and persisting until postnatal day 0. Changes in distribution reflected alterations in tangential migration and radial integration of GFP+ cells into the developing cortical plate. Fate mapping of GAD67GFP+ progenitors with bromodeoxyuridine injected at E13 demonstrated a significant increase of these cells at P0 in anterior white matter. An overall decrease in GAD67GFP+ progenitors at P0 in medial frontal cortex could not be attributed to a reduction in cell proliferation. Significant changes in dlx2, nkx2.1 and their downstream target erbb4, transcription factors which regulate interneuron migration, were found within the prenatally stressed developing forebrain, while no differences were seen in mash1, a determinant of interneuron fate, bdnf, a maturation factor for GABAergic cells or fgf2, an early growth/differentiation factor. These results demonstrate that early disruption in GABAergic progenitor migration caused by prenatal stress may be responsible for neuronal defects in disorders with GABAergic abnormalities like schizophrenia.

Indexed as

Cell MovementStress, PhysiologicalAnimalsAnimals, NewbornErbB ReceptorsFemaleGABAergic NeuronsMaleMiceNeocortexNeural Stem CellsPregnancyReceptor, ErbB-4Restraint, PhysicalTranscription FactorsErbb4 protein, mouseErbB ReceptorsReceptor, ErbB-4Transcription Factors

Identifiers

PMID22910687
PMCPMC3532962
OpenAlexW2069985888

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.