Evidence map›Paper›PMID 33890333›Full record

ArticleJournal of neuroendocrinology2021

Microglial synaptic pruning on axon initial segment spines of dentate granule cells: Sexually dimorphic effects of early-life stress and consequences for adult fear response.

Mario A Zetter, Vito S Hernández, Angélica Roque, Oscar R Hernández-Pérez, María J Gómora, Silvia Ruiz-Velasco, Lee E Eiden, Limei Zhang

Abstract read
In one paragraph

Article in Journal of neuroendocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Microglia as critical mediators linking perinatal immune stress to mental health trajectories.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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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

8 authors at 2 institutions in 2 countries.

Mario A ZetterDepartment of Physiology, School of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.ORCID 0000-0001-7132-5345
Vito S HernándezDepartment of Physiology, School of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.ORCID 0000-0002-1486-1659
Angélica RoqueDepartment of Physiology, School of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.ORCID 0000-0002-1149-4806
Oscar R Hernández-PérezDepartment of Physiology, School of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.ORCID 0000-0002-7998-422X
María J GómoraDepartment of Embryology, School of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.
Silvia Ruiz-VelascoDepartment of Probability and Statistics, Applied Mathematics and Systems Research Institute, National Autonomous University of Mexico, Mexico City, Mexico.ORCID 0000-0002-9220-2368
Lee E EidenSection on Molecular Neuroscience, Intramural Research Program, National Institute of Mental Health, NIH, Bethesda, MD, USA.ORCID 0000-0001-7524-944X
Limei ZhangDepartment of Physiology, School of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.ORCID 0000-0002-7422-5136
Universidad Nacional Autónoma de México · MXNational Institute of Mental Health · US

Funding

Chemical Coding Of NeurotransmissionZIAMH002386 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI EIDEN, LEE E. · 2009 to 2025
$25.6M
Intramural NIH HHS ZIA MH002386
6 · The paper itself

Abstract

Axon initial segments (AIS) of dentate granule cells in the hippocampus exhibit prominent spines (AISS) during early development that are associated with microglial contacts. In the present study, we investigated whether developmental changes in AISS could be modified by early-life stress (ELS), specifically neonatal maternal separation (MS), through stress hormones and microglial activation and examined the potential behavioural consequences. We examined AISS at postnatal day (PND)5, 15 and 50, using Golgi-Cox staining and anatomical analysis. Neurone-microglial interaction was assessed using antibodies against ankyrin-G, PSD-95 and Iba1, for AIS, AISS and microglia visualisation, respectively, in normally reared and neonatal maternally separated male and female rats. We observed a higher density of AISS in ELS rats at both PND15 and PND50 compared to controls. Effects were more pronounced in females than males. AIS-associated microglia in ELS rats showed a hyper-ramified morphology and less co-localisation with PSD-95 compared to controls at PND15. ELS-associated alteration in microglial morphology and synaptic pruning was mimicked by treatment of acute hippocampal slices of normally reared rats with vasopressin. ELS rats exhibited increased freezing behaviour during auditory fear memory testing, which was more pronounced in female subjects and corresponded with increased Fos expression in dorsal and ventral dentate granule cells. Thus, microglial synaptic pruning in dentate AIS of hippocampus is influenced by ELS, with demonstrable sex bias regarding its anatomical characteristics and subsequent fear-induced defensive behaviours.

Indexed as

Stress, PsychologicalAgingAnimalsAnimals, NewbornAxon Initial SegmentDendritic SpinesDentate GyrusFearFemaleMaleMaternal DeprivationMicrogliaNeuronal PlasticityPregnancyRatsRats, Wistarankyrin-Gauditory fear responseaxon initial segment spineIba1maternal separationvasopressin

Identifiers

PMID33890333
PMCPMC13186562
OpenAlexW3152717807

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.