4.7 Review

Impact of Maternal Immune Activation on Nonhuman Primate Prefrontal Cortex Development: Insights for Schizophrenia

Journal

BIOLOGICAL PSYCHIATRY
Volume 92, Issue 6, Pages 460-469

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2022.04.004

Keywords

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Funding

  1. University of California, Davis, Conte Center (National Institute of Mental Health) [P50MH106438, P50MH106438-06]
  2. University of California, Davis
  3. MIND Institute Intellectual and Developmental Disabilities Research Center (Eunice Kennedy Shriver National Institute of Child Health and Human Development) [P50HD103526]
  4. UC Davis Training Program in Learning, Memory, and Plasticity [T32 MH112507]

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Late adolescence is a period of dynamic changes in the brain, particularly in the prefrontal cortical regions, which orchestrate cognitive control. Early challenges may lead to aberrant PFC connectivity and function, while activation of the mother's immune system during pregnancy could contribute to an increased risk of neurodevelopmental disorders.
Late adolescence is a period of dynamic change in the brain as humans learn to navigate increasingly complex environments. In particular, prefrontal cortical (PFC) regions undergo extensive remodeling as the brain is fine-tuned to orchestrate cognitive control over attention, reasoning, and emotions. Late adolescence also presents a uniquely vulnerable period as neurodevelopmental illnesses, such as schizophrenia, become evident and worsen into young adulthood. Challenges in early development, including prenatal exposure to infection, may set the stage for a cascade of maladaptive events that ultimately result in aberrant PFC connectivity and function before symptoms emerge. A growing body of research suggests that activation of the mother's immune system during pregnancy may act as a disease primer, in combination with other environmental and genetic factors, contributing to an increased risk of neurodevelopmental disorders, including schizophrenia. Animal models provide an invaluable opportunity to examine the course of brain and behavioral changes in offspring exposed to maternal immune activation (MIA). Although the vast majority of MIA research has been carried out in rodents, here we highlight the translational utility of the nonhuman primate (NHP) as a model species more closely related to humans in PFC structure and function. In this review, we consider the protracted period of brain and behavioral maturation in the NHP, describe emerging findings from MIA NHP offspring in the context of rodent preclinical models, and lastly explore the translational relevance of the NHP MIA model to expand understanding of the etiology and developmental course of PFC pathology in schizophrenia.

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