Transgenerational modification of dopaminergic dysfunctions induced by maternal immune activation |
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Authors: | Ulrike Weber-Stadlbauer Juliet Richetto Ramona A. J. Zwamborn Roderick C. Slieker Urs Meyer |
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Affiliation: | 1.Institute of Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich, Switzerland ;2.Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland ;3.Department of Neurology, UMC Utrecht Brain Center, Utrecht, The Netherlands ;4.Department of Biomedical Data Sciences, Section Molecular Epidemiology, Leiden, The Netherlands ;5.Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands |
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Abstract: | Prenatal exposure to infectious and/or inflammatory insults is increasingly recognized to contribute to the etiology of psychiatric disorders with neurodevelopmental components. Recent research using animal models suggests that maternal immune activation (MIA) can induce transgenerational effects on brain and behavior, possibly through epigenetic mechanisms. Using a mouse model of MIA that is based on gestational treatment with the viral mimeticpoly(I:C) (= polyriboinosinic-polyribocytidilic acid), the present study explored whether the transgenerational effects of MIA are extendable to dopaminergic dysfunctions. We show that the direct descendants born to poly(I:C)-treated mothers display signs of hyperdopaminergia, as manifested by a potentiated sensitivity to the locomotor-stimulating effects of amphetamine (Amph) and increased expression of tyrosine hydroxylase (Th) in the adult ventral midbrain. In stark contrast, second- and third-generation offspring of MIA-exposed ancestors displayed blunted locomotor responses to Amph and reduced expression of Th. Furthermore, we found increased DNA methylation at the promoter region of the dopamine-specifying factor, nuclear receptor-related 1 protein (Nurr1), in the sperm of first-generation MIA offspring and in the ventral midbrain of second-generation offspring of MIA-exposed ancestors. The latter effect was further accompanied by reduced mRNA levels of Nurr1 in this brain region. Together, our results suggest that MIA has the potential to modify dopaminergic functions across multiple generations with opposite effects in the direct descendants and their progeny. The presence of altered DNA methylation in the sperm of MIA-exposed offspring highlights the possibility that epigenetic processes in the male germline play a role in the transgenerational effects of MIA.Subject terms: Neuroimmunology, Developmental disorders |
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