Evidence map›Paper›PMID 35963885›Full record

ArticlePediatric research2023

Maternal immune activation alters fetal and neonatal microglia phenotype and disrupts neurogenesis in mice.

Marco Loayza, Shuying Lin, Kathleen Carter, Norma Ojeda, Lir-Wan Fan, Sumana Ramarao, Abhay Bhatt, Yi Pang

Abstract read
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In one paragraph

Article in Pediatric research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
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  6. Immune dysfunction in Alzheimer disease.Nature reviews. Neuroscience · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Microglia as critical mediators linking perinatal immune stress to mental health trajectories.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  12. Article
  13. Article
  14. Review
  15. Microglial plasticity across development mediates infantile amnesia.bioRxiv : the preprint server for biology · 2025
    Article
  16. Review
  17. Article
  18. Article
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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 1 institution in 1 country.

Marco LoayzaDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, MS, 39216, USA.
Shuying LinDepartment of Physical Therapy, University of Mississippi Medical Center, Jackson, MS, 39216, USA.
Kathleen CarterDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, MS, 39216, USA.
Norma OjedaDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, MS, 39216, USA.
Lir-Wan FanDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, MS, 39216, USA.
Sumana RamaraoDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, MS, 39216, USA.
Abhay BhattDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, MS, 39216, USA. abhatt@umc.edu.
Yi PangDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, MS, 39216, USA. ypang@umc.edu.ORCID http://orcid.org/0000-0003-0453-6921
Jackson Memorial Hospital · US

Funding

Role of obesity in preeclamptic pregnancy.P20GM121334 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI Babbette LaMarca, Jane F Reckelhoff · 2017 to 2026
$26.4M
6 · The paper itself

Abstract

backgroundActivation of microglia, increase in cortical neuron density, and reduction in GABAergic interneurons are some of the key findings in postmortem autism spectrum disorders (ASD) subjects. The aim of this study was to investigate how maternal immune activation (MIA) programs microglial phenotypes and abnormal neurogenesis in offspring mice.

methodsMIA was induced by injection of lipopolysaccharide (LPS, i.p.) to pregnant mice at embryonic (E) day 12.5. Microglial phenotypes and neurogenesis were investigated between E15.5 to postnatal (P) day 21 by immunohistochemistry, flow cytometry, and cytokine array.

resultsMIA led to a robust increase in fetal and neonatal microglia in neurogenic regions. Homeostatic E15.5 and P4 microglia are heterogeneous, consisting of M1 (CD86+/CD206-) and mixed M1/M2 (CD86+/CD206+)-like subpopulations. MIA significantly reduced M1 but increased mixed M1/M2 microglia, which was associated with upregulation of numerous cytokines with pleotropic property. MIA resulted in a robust increase in Ki67+/Nestin+ and Tbr2+ neural progenitor cells in the subventricular zone (SVZ) of newborn mice. At juvenile stage, a male-specific reduction of Parvalbumin+ but increase in Reelin+ interneurons in the medial prefrontal cortex was found in MIA offspring mice.

conclusionsMIA programs microglia towards a pleotropic phenotype that may drive excessive neurogenesis in ASD patients. IMPACT: Maternal immune activation (MIA) alters microglial phenotypes in the brain of fetal and neonatal mouse offspring. MIA leads to excessive proliferation and overproduction of neural progenitors in the subventricular zone (SVZ). MIA reduces parvalbumin+ while increases Reelin+ interneurons in the prefrontal cortex. Our study sheds light on neurobiological mechanisms of abnormal neurogenesis in certain neurodevelopmental disorders, such as autism spectrum disorder (ASD).

Indexed as

Autism Spectrum DisorderPrenatal Exposure Delayed EffectsAnimalsCytokinesFemaleHumansMaleMiceMicrogliaNeurogenesisParvalbuminsPregnancyCytokinesParvalbumins

Identifiers

PMID35963885
OpenAlexW4291178034

What OpenQuestion holds

Textmetadata
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Registered trials

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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.