4.0 Article

Maternal immune activation downregulates schizophrenia genes in the foetal mouse brain

期刊

BRAIN COMMUNICATIONS
卷 3, 期 4, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/braincomms/fcab275

关键词

schizophrenia; genetics; maternal; immune; infection

资金

  1. National Institute for Health Research UK [CL-2019-13-001]
  2. John Fell Fund from the University of Oxford [H5D00080]
  3. Wellcome Trust Investigator Award [WT204969/Z/16/Z]
  4. Oxford Biomedical Research Centre and Chinese Academy of Medical Sciences (CAMS) Innovation Fund for Medical Science [2018-I2M-2-002]
  5. Wellcome Trust [090532/Z/09/Z, 203141/Z/16/Z]
  6. Health Data Research UK
  7. Oxford Biomedical Research Centre

向作者/读者索取更多资源

The study found that maternal immune activation mimicking viral infections can downregulate genes associated with schizophrenia, particularly those involved in neurodevelopment such as neuronal cell adhesion. These results provide insight into the interaction between genetic and environmental factors in schizophrenia pathogenesis.
Handunnetthi et al. find that schizophrenia genes are downregulated by maternal immune activation mimicking viral infections. These downregulated genes play key roles in neurodevelopmental processes such as neuronal cell adhesion. Overall, these findings provide insight into how genetic and environmental factors may interact in the causal cascade to schizophrenia. Susceptibility to schizophrenia is mediated by genetic and environmental risk factors. Maternal immune activation by infections during pregnancy is hypothesized to be a key environmental risk factor. However, little is known about how maternal immune activation contributes to schizophrenia pathogenesis. In this study, we investigated if maternal immune activation influences the expression of genes associated with schizophrenia in foetal mouse brains. We found that two sets of schizophrenia genes were downregulated more than expected by chance in the foetal mouse brain following maternal immune activation, namely those genes associated with schizophrenia through genome-wide association study (fold change = 1.93, false discovery rate = 4 x 10(-4)) and downregulated genes in adult schizophrenia brains (fold change = 1.51, false discovery rate = 4 x 10(-10)). We found that these genes mapped to key biological processes, such as neuronal cell adhesion. We also identified cortical excitatory neurons and inhibitory interneurons as the most vulnerable cell types to the deleterious effects of this interaction. Subsequently, we used gene expression information from herpes simplex virus 1 infection of neuronal precursor cells as orthogonal evidence to support our findings and to demonstrate that schizophrenia-associated cell adhesion genes, PCDHA2, PCDHA3 and PCDHA5, were downregulated following herpes simplex virus 1 infection. Collectively, our results provide novel evidence for a link between genetic and environmental risk factors in schizophrenia pathogenesis. These findings carry important implications for early preventative strategies in schizophrenia.

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