Developmental ethanol exposure has minimal impact on cerebellar microglial dynamics, morphology, and interactions with Purkinje cells during adolescence

• Published in: Frontiers in neuroscience Vol. 17; p. 1176581
• Main Authors: Cealie, MaKenna Y, Douglas, James C, Le, Linh H D, Vonkaenel, Erik D, McCall, Matthew N, Drew, Paul D, Majewska, Ania K
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 05.05.2023; Frontiers Media S.A
• Subjects: Animal models; Apoptosis; Cell activation; Cell death; Cell interactions; Cells; Central nervous system; Cerebellum; Child development; Cognitive ability; Cytology; Ethanol; Females; fetal alcohol spectrum disorders (FASD); Fetal alcohol syndrome; Immune response; immune system; Long-term effects; Males; Microglia; Morphology; Motility; Nervous system; Neurogenesis; Neuroscience; Purkinje cell; Purkinje cells; Surveillance; neurodevelopment; prenatal alcohol exposure; immune system; Purkinje cell; ethanol; microglia; cerebellum; fetal alcohol spectrum disorders (FASD)
• ISSN: 1662-4548; 1662-453X; 1662-453X
• DOI: 10.3389/fnins.2023.1176581

Fetal alcohol spectrum disorders (FASD) are the most common cause of non-heritable, preventable mental disability, occurring in almost 5% of births in the United States. FASD lead to physical, behavioral, and cognitive impairments, including deficits related to the cerebellum. There is no known cure for FASD and their mechanisms remain poorly understood. To better understand these mechanisms, we examined the cerebellum on a cellular level by studying microglia, the principal immune cells of the central nervous system, and Purkinje cells, the sole output of the cerebellum. Both cell types have been shown to be affected in models of FASD, with increased cell death, immune activation of microglia, and altered firing in Purkinje cells. While ethanol administered in adulthood can acutely depress the dynamics of the microglial process arbor, it is unknown how developmental ethanol exposure impacts microglia dynamics and their interactions with Purkinje cells in the long term. To address this question, we used a mouse model of human 3rd trimester exposure, whereby L7 /Ai9 /Cx3cr1 mice (with fluorescently labeled microglia and Purkinje cells) of both sexes were subcutaneously treated with a binge-level dose of ethanol (5.0 g/kg/day) or saline from postnatal days 4-9. Cranial windows were implanted in adolescent mice above the cerebellum to examine the long-term effects of developmental ethanol exposure on cerebellar microglia and Purkinje cell interactions using two-photon imaging. We found that cerebellar microglia dynamics and morphology were not affected after developmental ethanol exposure. Microglia dynamics were also largely unaltered with respect to how they interact with Purkinje cells, although subtle changes in these interactions were observed in females in the molecular layer of the cerebellum. This work suggests that there are limited long-term effects of ethanol exposure on microglia morphology, dynamics, and neuronal interactions, so other avenues of research may be important in elucidating the mechanisms of FASD.