Evidence map›Paper›PMID 38715090›Full record

ArticleJournal of neuroinflammation2024

Impact of maternal immune activation and sex on placental and fetal brain cytokine and gene expression profiles in a preclinical model of neurodevelopmental disorders.

Hadley C Osman, Rachel Moreno, Destanie Rose, Megan E Rowland, Annie Vogel Ciernia, Paul Ashwood

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

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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

6 authors.

Hadley C OsmanDepartment of Medical Microbiology and Immunology, University of California, Davis, Davis, CA, USA.
Rachel MorenoDepartment of Medical Microbiology and Immunology, University of California, Davis, Davis, CA, USA.
Destanie RoseDepartment of Medical Microbiology and Immunology, University of California, Davis, Davis, CA, USA.
Megan E RowlandDepartment of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, Canada.
Annie Vogel CierniaDepartment of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, Canada.
Paul AshwoodDepartment of Medical Microbiology and Immunology, University of California, Davis, Davis, CA, USA. pashwood@ucdavis.edu.

Funding

Immune regulation and autismR01MH118209 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ASHWOOD, PAUL · 2019 to 2023
$2.0M
Immune regulation and gastrointestinal co-morbidity in autism spectrum disordersR01HD090214 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ASHWOOD, PAUL · 2018 to 2022
$1.9M
Combined environmental exposures and neurodevelopment disordersR21ES035969 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ASHWOOD, PAUL · 2024 to 2025
$443k
The effects of wildfire exposure on maternal allergic asthma and consequences on neurobiologyR21ES035492 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ASHWOOD, PAUL · 2023 to 2023
$441k
The effects of environmental air pollutants on maternal allergic asthma and its neurobiological consequencesR21ES025560 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ASHWOOD, PAUL · 2017 to 2018
$432k
NICHD NIH HHS R01 HD090214NIEHS NIH HHS R21 ES025560NIEHS NIH HHS R21 ES035492NIEHS NIH HHS R21 ES035969NIMH NIH HHS R01 MH118209
6 · The paper itself

Abstract

Maternal inflammation during gestation is associated with a later diagnosis of neurodevelopmental disorders including autism spectrum disorder (ASD). However, the specific impact of maternal immune activation (MIA) on placental and fetal brain development remains insufficiently understood. This study aimed to investigate the effects of MIA by analyzing placental and brain tissues obtained from the offspring of pregnant C57BL/6 dams exposed to polyinosinic: polycytidylic acid (poly I: C) on embryonic day 12.5. Cytokine and mRNA content in the placenta and brain tissues were assessed using multiplex cytokine assays and bulk-RNA sequencing on embryonic day 17.5. In the placenta, male MIA offspring exhibited higher levels of GM-CSF, IL-6, TNFα, and LT-α, but there were no differences in female MIA offspring. Furthermore, differentially expressed genes (DEG) in the placental tissues of MIA offspring were found to be enriched in processes related to synaptic vesicles and neuronal development. Placental mRNA from male and female MIA offspring were both enriched in synaptic and neuronal development terms, whereas females were also enriched for terms related to excitatory and inhibitory signaling. In the fetal brain of MIA offspring, increased levels of IL-28B and IL-25 were observed with male MIA offspring and increased levels of LT-α were observed in the female offspring. Notably, we identified few stable MIA fetal brain DEG, with no male specific difference whereas females had DEG related to immune cytokine signaling. Overall, these findings support the hypothesis that MIA contributes to the sex- specific abnormalities observed in ASD, possibly through altered neuron developed from exposure to inflammatory cytokines. Future research should aim to investigate how interactions between the placenta and fetal brain contribute to altered neuronal development in the context of MIA.

Indexed as

BrainCytokinesMice, Inbred C57BLNeurodevelopmental DisordersPlacentaPrenatal Exposure Delayed EffectsSex CharacteristicsAnimalsDisease Models, AnimalFemaleFetusMaleMicePoly I-CPregnancyTranscriptomeCytokinesPoly I-CAutismAutism spectrum disorder (ASD)CytokinesDevelopmentFetal brainMaternal immune activationMIANeurodevelopmentPlacentaSchizophreniaSynapse

Identifiers

PMID38715090
PMCPMC11077729

What OpenQuestion holds

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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.