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Induction of Maternal Immune Activation in Mice at Mid-gestation Stage with Viral Mimic Poly(I:C)
Published on: March 25, 2016
Prenatal Immune and Endocrine Modulators of Offspring's Brain Development and Cognitive Functions Later in Life
Steven Schepanski1,2, Claudia Buss3,4, Ileana L Hanganu-Opatz2
1Laboratory of Experimental Feto-Maternal Medicine, Department of Obstetrics and Fetal Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Insights
Prenatal challenges impact offspring brain development via maternal hormones and immune cells. These factors can cause lasting cognitive and behavioral changes, potentially through epigenetic inheritance.
Area of Science:
- Neuroimmunology
- Developmental Neuroscience
- Epigenetics
Background:
- Prenatal challenges like maternal stress or infection can negatively affect offspring cognitive development and behavior.
- Fetal brain development is sensitive to maternal factors transferred across the placenta, including hormones and immune cells.
- Maternal microchimeric cells, present in the fetal brain, may play a role in mediating these effects.
Purpose of the Study:
- To explore the role of maternal hormones and immune markers in modulating fetal brain development under prenatal stress.
- To investigate the potential for epigenetic inheritance of altered brain development across generations.
- To highlight the significance of maternal microchimeric cells in neurodevelopmental outcomes.
Main Methods:
- Review of existing literature on maternal-fetal transfer of hormones and immune cells.
- Analysis of studies investigating the impact of prenatal challenges on offspring neurodevelopment and behavior.
- Discussion of emerging evidence on maternal microchimeric cells and epigenetic modifications.
Main Results:
- Maternal hormones (e.g., glucocorticoids) and immune markers (cytokines, cells) can cross the placenta, influencing fetal brain development.
- Maternal microchimeric cells in the fetal brain may alter neurodevelopment and post-natal cognitive functions.
- Prenatal stress can induce multi-generational epigenetic changes in brain development, independent of genetics.
Conclusions:
- Maternal factors transferred vertically significantly impact fetal brain development and long-term cognitive functions.
- Maternal microchimeric cells represent a novel pathway influencing neurodevelopment and behavior.
- Epigenetic mechanisms are crucial in transmitting the effects of prenatal challenges across generations.
Abstract:
Milestones of brain development in mammals are completed before birth, which provide the prerequisite for cognitive and intellectual performances of the offspring. Prenatal challenges, such as maternal stress experience or infections, have been linked to impaired cognitive development, poor intellectual performances as well as neurodevelopmental and psychiatric disorders in the offspring later in life. Fetal microglial cells may be the target of such challenges and could be functionally modified by maternal markers. Maternal markers can cross the placenta and reach the fetus, a phenomenon commonly referred to as "vertical transfer." These maternal markers include hormones, such as glucocorticoids, and also maternal immune cells and cytokines, all of which can be altered in response to prenatal challenges. Whilst it is difficult to discriminate between the maternal or fetal origin of glucocorticoids and cytokines in the offspring, immune cells of maternal origin-although low in frequency-can be clearly set apart from offspring's cells in the fetal and adult brain. To date, insights into the functional role of these cells are limited, but it is emergingly recognized that these maternal microchimeric cells may affect fetal brain development, as well as post-natal cognitive performances and behavior. Moreover, the inheritance of vertically transferred cells across generations has been proposed, yielding to the presence of a microchiome in individuals. Hence, it will be one of the scientific challenges in the field of neuroimmunology to identify the functional role of maternal microchimeric cells as well as the brain microchiome. Maternal microchimeric cells, along with hormones and cytokines, may induce epigenetic changes in the fetal brain. Recent data underpin that brain development in response to prenatal stress challenges can be altered across several generations, independent of a genetic predisposition, supporting an epigenetic inheritance. We here discuss how fetal brain development and offspring's cognitive functions later in life is modulated in the turnstile of prenatal challenges by introducing novel and recently emerging pathway, involving maternal hormones and immune markers.
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