Maternal immune activation in mice delays myelination and axonal development in the hippocampus of the offspring

Epidemiological data suggest a relationship between maternal infection and a high incidence of schizophrenia in offspring. An animal model based on this hypothesis was made by injecting double‐stranded RNA, polyinosinic‐polycytidylic acid (poly‐I:C), into early pregnant mice, and their offspring were examined for biochemical and histological abnormalities. Mouse brains were examined with special reference to oligodendrocytes, which have been implicated in several neurodevelopmental disorders. We detected a significant decrease of myelin basic protein (MBP) mRNA and protein at early postnatal periods in poly‐I:C mice. MBP immunocytochemistry and electron microscopy revealed that the hippocampus of juvenile poly‐I:C mice was less myelinated than in PBS mice, with no significant loss of oligodendrocytes. In addition, axonal diameters were significantly smaller in juvenile poly‐I:C mice than in control mice. These abnormalities reverted to normal levels when the animals reached the adult stage. These findings suggest that retarded myelination and axonal abnormalities in early postnatal stages caused by maternal immune activation could be related to schizophrenia‐related behaviors in adulthood. © 2008 Wiley‐Liss, Inc.

[1]  J. Feldon,et al.  Adult behavioral and pharmacological dysfunctions following disruption of the fetal brain balance between pro-inflammatory and IL-10-mediated anti-inflammatory signaling , 2008, Molecular Psychiatry.

[2]  K. Mirnics,et al.  Maternal Immune Activation Alters Fetal Brain Development through Interleukin-6 , 2007, The Journal of Neuroscience.

[3]  Bryan M Hooks,et al.  Loss of erbB signaling in oligodendrocytes alters myelin and dopaminergic function, a potential mechanism for neuropsychiatric disorders , 2007, Proceedings of the National Academy of Sciences.

[4]  C. Beglinger,et al.  Effects of budesonide on P‐glycoprotein expression in intestinal cell lines , 2007, British journal of pharmacology.

[5]  K. Davis,et al.  The human homolog of the QKI gene affected in the severe dysmyelination "quaking" mouse phenotype: downregulated in multiple brain regions in schizophrenia. , 2006, The American journal of psychiatry.

[6]  Urs Meyer,et al.  The Time of Prenatal Immune Challenge Determines the Specificity of Inflammation-Mediated Brain and Behavioral Pathology , 2006, The Journal of Neuroscience.

[7]  K. Hashimoto,et al.  Immune Activation During Pregnancy in Mice Leads to Dopaminergic Hyperfunction and Cognitive Impairment in the Offspring: A Neurodevelopmental Animal Model of Schizophrenia , 2006, Biological Psychiatry.

[8]  Urs Meyer,et al.  Towards an immuno-precipitated neurodevelopmental animal model of schizophrenia , 2005, Neuroscience & Biobehavioral Reviews.

[9]  Vahram Haroutunian,et al.  Variations in myelin and oligodendrocyte-related gene expression across multiple brain regions in schizophrenia: A gene ontology study , 2005, Schizophrenia Research.

[10]  N. Daw,et al.  Experience-Driven Plasticity of Visual Cortex Limited by Myelin and Nogo Receptor , 2005, Science.

[11]  Yasuhiro Kawasaki,et al.  Differential contributions of prefrontal and temporolimbic pathology to mechanisms of psychosis. , 2005, Brain : a journal of neurology.

[12]  Peter J. Brophy,et al.  Mechanisms of axon ensheathment and myelin growth , 2005, Nature Reviews Neuroscience.

[13]  I. Weiner,et al.  Maternal immune activation leads to behavioral and pharmacological changes in the adult offspring. , 2005, Journal of psychiatric research.

[14]  Charles P Quesenberry,et al.  Maternal exposure to toxoplasmosis and risk of schizophrenia in adult offspring. , 2005, The American journal of psychiatry.

[15]  S. Akira,et al.  Involvement of Toll-like Receptor 3 in the Immune Response of Lung Epithelial Cells to Double-stranded RNA and Influenza A Virus* , 2005, Journal of Biological Chemistry.

[16]  Yue Feng,et al.  Developmental Abnormalities of Myelin Basic Protein Expression in fyn Knock-out Brain Reveal a Role of Fyn in Posttranscriptional Regulation* , 2005, Journal of Biological Chemistry.

[17]  Nora I. Perrone-Bizzozero,et al.  Altered Myelination of the Hippocampal Formation in Subjects with Schizophrenia and Bipolar Disorder , 2004, Neurochemical Research.

[18]  Stephen Kent,et al.  The viral mimic, polyinosinic:polycytidylic acid, induces fever in rats via an interleukin-1-dependent mechanism. , 2004, American journal of physiology. Regulatory, integrative and comparative physiology.

[19]  A. Kakita,et al.  Prefrontal Abnormality of Schizophrenia Revealed by DNA Microarray: Impact on Glial and Neurotrophic Gene Expression , 2004, Annals of the New York Academy of Sciences.

[20]  P. Brophy New Roles for an Old Molecule in Axon-Glial Interaction , 2004, Neuron.

[21]  R. Sidwell,et al.  Glial fibrillary acidic protein and glutamic acid decarboxylase 65 and 67 kDa proteins are increased in brains of neonatal BALB/c mice following viral infection in utero , 2004, Schizophrenia Research.

[22]  M. Ikawa,et al.  The LIM homeobox gene, L3/Lhx8, is necessary for proper development of basal forebrain cholinergic neurons , 2004, The European journal of neuroscience.

[23]  I. Weiner,et al.  Immune Activation During Pregnancy in Rats Leads to a PostPubertal Emergence of Disrupted Latent Inhibition, Dopaminergic Hyperfunction, and Altered Limbic Morphology in the Offspring: A Novel Neurodevelopmental Model of Schizophrenia , 2003, Neuropsychopharmacology.

[24]  Peter B. Jones,et al.  Oligodendrocyte dysfunction in schizophrenia and bipolar disorder , 2003, The Lancet.

[25]  H. Takebayashi,et al.  Evidence for a second wave of oligodendrogenesis in the postnatal cerebral cortex of the mouse , 2003, Journal of neuroscience research.

[26]  Ryan Remedios,et al.  Expression of FGF Receptors 1, 2, 3 in the Embryonic and Postnatal Mouse Brain Compared with Pdgfrα, Olig2 and Plp/dm20: Implications for Oligodendrocyte Development , 2003, Developmental Neuroscience.

[27]  Philip D. Harvey,et al.  White matter changes in schizophrenia: evidence for myelin-related dysfunction. , 2003, Archives of general psychiatry.

[28]  E. Susser,et al.  Serologic evidence for prenatal influenza in the etiology of schizophrenia , 2003, Schizophrenia Research.

[29]  E. Susser,et al.  Elevated maternal interleukin-8 levels and risk of schizophrenia in adult offspring , 2003, Schizophrenia Research.

[30]  Limin Shi,et al.  Maternal Influenza Infection Causes Marked Behavioral and Pharmacological Changes in the Offspring , 2003, The Journal of Neuroscience.

[31]  M. Calcagnotto,et al.  Heterotopic Neurons with Altered Inhibitory Synaptic Function in an Animal Model of Malformation-Associated Epilepsy , 2002, The Journal of Neuroscience.

[32]  D. Weinberger,et al.  Neonatal hippocampal damage alters electrophysiological properties of prefrontal cortical neurons in adult rats. , 2002, Cerebral cortex.

[33]  J. Simon,et al.  Increased hippocampal volume in schizophrenics' parents with ancestral history of schizophrenia , 2002, Schizophrenia Research.

[34]  D. Weinberger,et al.  Effects of Reversible Inactivation of the Neonatal Ventral Hippocampus on Behavior in the Adult Rat , 2002, The Journal of Neuroscience.

[35]  G. Barker,et al.  Investigating regional white matter in schizophrenia using diffusion tensor imaging , 2002, Neuroreport.

[36]  Limin Shi,et al.  Prenatal Viral Infection Leads to Pyramidal Cell Atrophy and Macrocephaly in Adulthood: Implications for Genesis of Autism and Schizophrenia , 2002, Cellular and Molecular Neurobiology.

[37]  S. Goderie,et al.  Multipotent Stem Cells from the Mouse Basal Forebrain Contribute GABAergic Neurons and Oligodendrocytes to the Cerebral Cortex during Embryogenesis , 2001, The Journal of Neuroscience.

[38]  R. Yolken,et al.  Maternal infections and subsequent psychosis among offspring. , 2001, Archives of general psychiatry.

[39]  B. Pearce,et al.  Schizophrenia and viral infection during neurodevelopment: a focus on mechanisms , 2001, Molecular Psychiatry.

[40]  N. Uranova,et al.  Electron microscopy of oligodendroglia in severe mental illness , 2001, Brain Research Bulletin.

[41]  W H Wong,et al.  Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[42]  E. Susser,et al.  Prenatal rubella, premorbid abnormalities, and adult schizophrenia , 2001, Biological Psychiatry.

[43]  S. Ebner,et al.  Distinct roles for PI3K in proliferation and survival of oligodendrocyte progenitor cells , 2000, Journal of neuroscience research.

[44]  T. Okamoto,et al.  Akt-Mediated Survival of Oligodendrocytes Induced by Neuregulins , 2000, The Journal of Neuroscience.

[45]  J. Foong,et al.  Neuropathological abnormalities of the corpus callosum in schizophrenia: a diffusion tensor imaging study , 2000, Journal of neurology, neurosurgery, and psychiatry.

[46]  Nikos Makris,et al.  Thalamic and amygdala–hippocampal volume reductions in first-degree relatives of patients with schizophrenia: an MRI-based morphometric analysis , 1999, Biological Psychiatry.

[47]  J. Suvisaari,et al.  Association between prenatal exposure to poliovirus infection and adult schizophrenia. , 1999, The American journal of psychiatry.

[48]  O. Arnold Schizophrenia – A Disturbance of Signal Interaction between the Entorhinal Cortex and the Dentate Gyrus? The Contribution of Experimental Dibenamine Psychosis to the Pathogenesis of Schizophrenia: A Hypothesis , 1999, Neuropsychobiology.

[49]  A. D. de Crespigny,et al.  Compromised white matter tract integrity in schizophrenia inferred from diffusion tensor imaging. , 1999, Archives of general psychiatry.

[50]  D. Weinberger,et al.  Cell biology of the hippocampal formation in schizophrenia , 1999, Biological Psychiatry.

[51]  C. Pantelis,et al.  Hippocampal volume in first-episode psychoses and chronic schizophrenia: a high-resolution magnetic resonance imaging study. , 1999, Archives of general psychiatry.

[52]  Daniel R. Weinberger,et al.  Neonatal lesions of the rat ventral hippocampus result in hyperlocomotion and deficits in social behaviour in adulthood , 1997, Psychopharmacology.

[53]  Edward D. Levin,et al.  Cognitive Effects of Neonatal Hippocampal Lesions in a Rat Model of Schizophrenia , 1996, Neuropsychopharmacology.

[54]  D. Weinberger,et al.  From neuropathology to neurodevelopment , 1995, The Lancet.

[55]  R. Murray,et al.  Does prenatal exposure to influenza in mice induce pyramidal cell disarray in the dorsal hippocampus? , 1995, Schizophrenia Research.

[56]  R. Murray,et al.  A neurodevelopmental approach to the classification of schizophrenia. , 1992, Schizophrenia bulletin.

[57]  D. Javitt,et al.  Recent advances in the phencyclidine model of schizophrenia. , 1991, The American journal of psychiatry.

[58]  D. Weinberger Implications of normal brain development for the pathogenesis of schizophrenia. , 1987, Archives of general psychiatry.

[59]  B. Bogerts,et al.  Basal Ganglia and Limbic System Pathology in Schizophrenia: A Morphometric Study of Brain Volume and Shrinkage , 1985 .

[60]  E. Susser,et al.  A.E. Bennett Research Award. Prenatal rubella, premorbid abnormalities, and adult schizophrenia. , 2001, Biological psychiatry.

[61]  E. Emamian,et al.  Defective corticogenesis and reduction in Reelin immunoreactivity in cortex and hippocampus of prenatally infected neonatal mice , 1999, Molecular Psychiatry.

[62]  S. Snyder,et al.  Amphetamine psychosis: a "model" schizophrenia mediated by catecholamines. , 1973, The American journal of psychiatry.