4.7 Article

Prefrontal microglia deficiency during adolescence disrupts adult cognitive functions and synaptic structures: A follow-up study in female mice

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 111, Issue -, Pages 230-246

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2023.04.007

Keywords

Cognitive functions; Clodronate; Microglia depletion; Prefrontal cortex; Sensitive periods; Synaptic pruning; Schizophrenia

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The prefrontal cortex (PFC) in the brain plays an important role in cognitive processes and matures throughout adolescence to early adulthood. Recent research using a mouse model shows that microglia, a type of brain cell, contribute to the maturation of the PFC in males. This study aimed to investigate whether microglia have a similar role in the maturation of the female PFC. The findings demonstrate that transient depletion of microglia during a specific window of adolescence disrupts cognitive functions and synaptic structures in the female PFC.
The prefrontal cortex (PFC) provides executive top-down control of a variety of cognitive processes. A distinctive feature of the PFC is its protracted structural and functional maturation throughout adolescence to early adulthood, which is necessary for acquiring mature cognitive abilities. Using a mouse model of cell-specific, transient and local depletion of microglia, which is based on intracerebral injection of clodronate disodium salt (CDS) into the PFC of adolescent male mice, we recently demonstrated that microglia contribute to the functional and structural maturation of the PFC in males. Because microglia biology and cortical maturation are partly sexually dimorphic, the main objective of the present study was to examine whether microglia similarly regulate this maturational process in female mice as well. Here, we show that a single, bilateral intra-PFC injection of CDS in adolescent (6-week-old) female mice induces a local and transient depletion (70 to 80% decrease from controls) of prefrontal microglia during a restricted window of adolescence without affecting neuronal or astrocytic cell populations. This transient microglia deficiency was sufficient to disrupt PFCassociated cognitive functions and synaptic structures at adult age. Inducing transient prefrontal microglia depletion in adult female mice did not cause these deficits, demonstrating that the adult PFC, unlike the adolescent PFC, is resilient to transient microglia deficiency in terms of lasting cognitive and synaptic maladaptations. Together with our previous findings in males, the present findings suggest that microglia contribute to the maturation of the female PFC in a similar way as to the prefrontal maturation occurring in males.

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