Evidence map›Paper›PMID 32860938›Full record

ArticleBrain, behavior, and immunity2020

Neonatal immune challenge induces female-specific changes in social behavior and somatostatin cell number.

Caroline J Smith, Marcy A Kingsbury, Julia E Dziabis, Richa Hanamsagar, Karen E Malacon, Jessica N Tran, Haley A Norris, Mary Gulino, Evan A Bordt, Staci D Bilbo

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

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  19. Oxytocin and microglia in the development of social behaviour.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Caroline J SmithDuke University, Department of Psychology and Neuroscience, Durham, NC, USA.
Marcy A KingsburyLurie Center for Autism, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Julia E DziabisDuke University, Department of Psychology and Neuroscience, Durham, NC, USA.
Richa HanamsagarDuke University, Department of Psychology and Neuroscience, Durham, NC, USA.
Karen E MalaconDuke University, Department of Psychology and Neuroscience, Durham, NC, USA.
Jessica N TranLurie Center for Autism, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Haley A NorrisLurie Center for Autism, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Mary GulinoLurie Center for Autism, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Evan A BordtLurie Center for Autism, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Staci D BilboDuke University, Department of Psychology and Neuroscience, Durham, NC, USA. Electronic address: Staci.bilbo@duke.edu.
Duke University · USHarvard University · USCenter for Autism and Related Disorders · US

Funding

Environmental Toxins and Microglia-Synapse Interactions in AutismR01ES025549 · NIEHS · MASSACHUSETTS GENERAL HOSPITAL · PI BILBO, STACI D, DZIRASA, KAFUI · 2016 to 2020
$2.1M
Sex Differences in Developing Microglia: Implications for Synaptic PruningR01MH101183 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI BILBO, STACI D · 2013 to 2017
$2.0M
The Microglial Developmental Index: A Novel Framework for Understanding the Role of Microglia in the Etiology of Autism Spectrum DisorderF32ES029912 · NIEHS · DUKE UNIVERSITY · PI SMITH, CAROLINE JACKSON · 2019 to 2020
$129k
NIEHS NIH HHS F32 ES029912NIEHS NIH HHS R01 ES025549NIMH NIH HHS R01 MH101183
6 · The paper itself

Abstract

Decreases in social behavior are a hallmark aspect of acute "sickness behavior" in response to infection. However, immune insults that occur during the perinatal period may have long-lasting consequences for adult social behavior by impacting the developmental organization of underlying neural circuits. Microglia, the resident immune cells of the central nervous system, are sensitive to immune stimulation and play a critical role in the developmental sculpting of neural circuits, making them likely mediators of this process. Here, we investigated the impact of a postnatal day (PND) 4 lipopolysaccharide (LPS) challenge on social behavior in adult mice. Somewhat surprisingly, neonatal LPS treatment decreased sociability in adult female, but not male mice. LPS-treated females also displayed reduced social interaction and social memory in a social discrimination task as compared to saline-treated females. Somatostatin (SST) interneurons within the anterior cingulate cortex (ACC) have recently been suggested to modulate a variety of social behaviors. Interestingly, the female-specific changes in social behavior observed here were accompanied by an increase in SST interneuron number in the ACC. Finally, these changes in social behavior and SST cell number do not appear to depend on microglial inflammatory signaling, because microglia-specific genetic knock-down of myeloid differentiation response protein 88 (MyD88; the removal of which prevents LPS from increasing proinflammatory cytokines such as TNFα and IL-1β) did not prevent these LPS-induced changes. This study provides novel evidence for enduring effects of neonatal immune activation on social behavior and SST interneurons in females, largely independent of microglial inflammatory signaling.

Indexed as

SomatostatinSomatostatin-Secreting CellsAnimalsCell CountFemaleLipopolysaccharidesMiceMicrogliaPregnancySocial BehaviorLipopolysaccharidesSomatostatinAnterior cingulate cortexLPSMicrogliaNeonatal immune challengeSex differencesSocial behaviorSomatostatin

Identifiers

PMID32860938
PMCPMC7556772
OpenAlexW3080311606

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.