Method Article

Generating a Reproducible Model of Mid-Gestational Maternal Immune Activation using Poly(I:C) to Study Susceptibility and Resilience in Offspring

DOI:

10.3791/64095

August 17th, 2022

In This Article

Summary

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Maternal infection is a risk factor for neurodevelopmental disorders. Mouse models of maternal immune activation (MIA) may elucidate infection's impact on brain development and function. Here, general guidelines and a procedure are provided to produce reliably resilient and susceptible offspring exposed to MIA.

Abstract

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Maternal immune activation (MIA) during pregnancy is consistently linked to increased risk of neurodevelopmental and neuropsychiatric disorders in offspring. Animal models of MIA are used to test causality, investigate mechanisms, and develop diagnostics and treatments for these disorders. Despite their widespread use, many MIA models suffer from a lack of reproducibility and almost all ignore two important aspects of this risk factor: (i) many offspring are resilient to MIA, and (ii) susceptible offspring can exhibit distinct combinations of phenotypes. To increase reproducibility and model both susceptibility and resilience to MIA, the baseline immunoreactivity (BIR) of female mice before pregnancy is used to predict which pregnancies will result in either resilient offspring or offspring with defined behavioral and molecular abnormalities after exposure to MIA. Here, a detailed method of inducing MIA via intraperitoneal (i.p.) injection of the double stranded RNA (dsRNA) viral mimic poly(I:C) at 12.5 days of gestation is provided. This method induces an acute inflammatory response in the dam, which results in perturbations in brain development in mice that map onto similarly impacted domains in human psychiatric and neurodevelopmental disorders (NDDs).

Introduction

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Epidemiological evidence links maternal infection to increased risk of psychiatric and NDDs, including schizophrenia (SZ) and autism spectrum disorder (ASD)1,2,3,4,5,6,7. The MIA mouse model was developed to test causality and the mechanistic role of MIA in the etiology of these disorders, as well as to identify molecular biomarkers and develop both diagnostic and therapeutic tools4,6

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Protocol

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All protocols are performed under the approval of the University of California-Davis Institutional Animal Care and Use Committee (IACUC).

1. Animal preparation

  1. When acquiring animals, keep the following parameters consistent to ensure maximal reproducibility.
    1. Vendor and vendor location: as previously reported, wild type C57BL/6J mice exhibit different responses to the same dose of poly(I:C) depending on the vendor8. Choose a vendor and mouse strain which show a consistent response. For the experiments here, C57BL/6 mice obtained from Charles River exhibited consistent changes ....

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Results

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Not all animals exposed to 30 mg/kg of poly(I:C) at E12.5 produce offspring with consistent behavioral abnormalities8,31. Though both 30 mg/kg and 40 mg/kg of poly(I:C) reliably produce sickness behaviors in dams, including decreased activity levels, hypothermic responses, and weight loss, and also cause significant elevations in IL-6, only a subset of litters exposed to MIA will go on to develop behavioral abnormalities in domains similar to those observed in hu.......

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Discussion

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Maternal infection alters the course of brain development in humans and in both rodents and nonhuman primates4,5,7. Here, a procedure to induce MIA in mice at a mid-gestational time point using poly(I:C) is outlined. This method incorporates assessment of BIR before pregnancy, which increases reproducibility and offers the chance to mechanistically investigate mechanisms that lead to resilience and susceptibility of offspring to.......

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Disclosures

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The authors have no conflicts of interest to disclose.

Acknowledgements

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We thank Dr. Myka Estes for her persistence in addressing variability in the mouse MIA model and all of the contributors in Estes et al.8 for their work that led to the development of the methods protocol described here. The research reported here was supported by NIMH 2P50 MH106438-06 (A.K.M.) and NIMH T32MH112507 (K.P.).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
0.9% NaCl physiological endotoxin free salineSigma-Aldrich7647-14-5Control and vehicle for Poly(I:C)
35mm petri dishThomas Scientific1219Z45Used to hold oil during tail bleed
7.5% TGX gelsBio-rad4561084Optional
Ancare NestletsFisher ScientificNC9365966Optional
anti-β-tubulinMilliporeMAB3408Optional
Bio-Plex Pro Mouse Cytokine Standards Group IBio-rad171I50001
Bio-Plex Pro Reagent Kit with Flat PlateBio-rad171304070M
Bovine Serum AlbuminThermoFisher23209Optional
CentrifugeEppendorf5810ROptional
Covidien Monoject 1/2 mL Insulin Syringe with 28G x 1/2 in. NeedleSpectrum552-58457-083
DithiothreitolSigma-AldrichD9779-10GOptional
Environmental enrichmentBio-servK3327 and K3322Optional
EthovisionNoldusEthovisionOptional
Fluorsecent-tagged seondary ntibodiesLi-cor925-32213 and 925-68072Optional
Food-grade edible oil (like olive, canola or grapeseed)Various vendorsUse to lubricate tail during tail bleeds
HBSSThermoFisher14060040Optional
High molecular weight polyinositic:polycytidilic acidInvivogen#tlrl-pic-5Used to establish females' BIR
Humane Mouse RestrainerAIMS1000Used to restrain mouse during tail bleeds
Image Studio SoftwareLicor5.2Optional
Laemmli bufferBio-rad1610737EDUOptional
Luminex200ThermoFisherAPX10031
Microvette CB300 300μl Serum capillary tubeSarstedt16.440.100
Mixed molecular weight polyinositic:polycytidilic acidSigma-Aldrich#P0913Gestational induction of MIA
monoclonal anti-MEF2AAbCamab76063Optional
monoclonal anti-STAT3Cell signaling12640SOptional
ObserverNoldusObserverOptional
Odyssey blocking buffer (TBS)Li-cor927-50003Optional
Odyssey CLx imaging systemLi-cor9140Optional
Omnipure PBSMillipore65054LOptional
Pierce BCA Protein Assay KitThermoFisher23227Optional
polyclonal anti_THPel-FreezP4101-150Optional
PVDF membraneBio-rad162-0177Optional
Qsonica Sonicator Q500Fisher Scientific15-338-282Optional
Quick blood stopperPetco17140
Seal-Rite 1.5 ml microcentrifuge tube, natural non-sterileUSA Scientific1615-5500
Soldering standAmazonB08Y12QC73Used to hold capillary tube during tail bleeds
Sunflower seedsBio-servS5137-1Use to increase breeding efficiency
The Bio-Plex Pro Mouse IL-6 set,Bio-rad171G5007M
Tris baseFisher ScientificBP152-1Optional
Tween 20Bio-rad23209Optional

References

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  1. Adams, W., Kendell, R. E., Hare, E. H., Munk-Jørgensen, P. Epidemiological evidence that maternal influenza contributes to the aetiology of schizophrenia. An analysis of Scottish, English, and Danish data. The British Journal of Psychiatry: The Journal of Mental Science. 163 (4), 522-534 (1993).
  2. Brown, A. S., et al.

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Tags

Poly I C ModelNeurodevelopmental DisordersMouse Pregnancy ModelOffspring SusceptibilityOffspring ResilienceBaseline ImmunoreactivityIntraperitoneal InjectionAcute Inflammatory ResponseBrain Development

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