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Induction of Maternal Immune Activation in Mice at Mid-gestation Stage with Viral Mimic PolyI:C
Published on: March 25, 2016
Subtle alterations in neonatal neurodevelopment following early or late exposure to prenatal maternal immune
Elisa Guma1, Emily Snook2, Shoshana Spring3
1Computational Brain Anatomy Laboratory, Cerebral Imaging Center, Douglas Mental Health University Institute, Montreal, Quebec, Canada; Integrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.
Insights
Maternal immune activation (MIA) during pregnancy subtly impacts neonatal mouse brain development and communication. Offspring show reduced vocalizations, but brain anatomy is largely unaffected in the neonatal period.
Area of Science:
- Neuroscience
- Developmental Biology
- Immunology
Background:
- Maternal immune activation (MIA) is linked to neurodevelopmental disorders.
- The impact of MIA timing on neonatal brain development requires further investigation.
Purpose of the Study:
- To investigate the effects of prenatal MIA on neonatal mouse brain development and behavior.
- To assess communicative abilities and brain anatomy in neonates exposed to MIA.
Main Methods:
- Utilized a mouse model of MIA.
- Assessed neonatal communicative abilities using ultrasonic vocalization tasks.
- Performed high-resolution ex vivo MRI on neonatal brains (postnatal day 8).
Main Results:
- Offspring exposed to MIA exhibited decreased communicative abilities.
- Neonatal brain anatomy was largely unaffected, with only subtle alterations observed.
- Both early and late MIA exposure resulted in subtle neuroanatomical and behavioral effects.
Conclusions:
- Prenatal MIA has subtle effects on neonatal neurodevelopment.
- Observed deficits in later life may be dormant or not yet apparent in the neonatal period.
- Integrated MRI and behavioral assays provide insights into early-life MIA impacts.
Abstract:
Prenatal exposure to maternal immune activation (MIA) is a risk factor for a variety of neurodevelopmental and psychiatric disorders. The timing of MIA-exposure has been shown to affect adolescent and adult offspring neurodevelopment, however, less is known about these effects in the neonatal period. To better understand the impact of MIA-exposure on neonatal brain development in a mouse model, we assess neonate communicative abilities with the ultrasonic vocalization task, followed by high-resolution ex vivo magnetic resonance imaging (MRI) on the neonatal (postnatal day 8) mouse brain. Early exposed offspring displayed decreased communicative ability, while brain anatomy appeared largely unaffected, apart from some subtle alterations. By integrating MRI and behavioural assays to investigate the effects of MIA-exposure on neonatal neurodevelopment we show that offspring neuroanatomy and behaviour are only subtly affected by both early and late exposure. This suggests that the deficits often observed in later stages of life may be dormant, not yet developed in the neonatal period, or not as easily detectable using a cross-sectional approach.
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