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Dean, L. E.

Publications and source records attributed to Dean, L. E..

2 recordsLinked to original sources

Ramping up the Heat: Induction of Systemic and Pulmonary Immune Responses and Metabolic Adaptations in Mice

Heatwaves pose a growing risk to public health. While most animal studies use sudden, extreme heat exposure, the systemic and pulmonary impacts of gradual heat exposures, reflective of real-world conditions, remain poorly characterized. This study examined the effects of acute, gradual extreme heat exposure to mice. Adult male and female C57Bl/6 mice were randomly assigned to heat-exposed, control, or pair-fed groups. Heat-exposed mice experienced a controlled 8-hour temperature ramp from 20{degrees}C to 38{degrees}C, mimicking the daily transition from nighttime lows to daytime highs. Control and pair-fed mice were maintained in parallel at ambient temperature. Multi-omics profiling was performed to assess cytokine levels in lung and serum, cecal microbiome composition, lung transcriptomics, and serum metabolomics. Heat exposure significantly altered the levels of multiple cytokines in serum and lung, including IL-17, MIP-1, MIP-1{beta}, IL-1, IL-12(p40), and RANTES, indicating shifts in mucosal immunity and immune cell recruitment. Random forest analysis identified 20 taxa that distinguished experimental groups, with a reduction in Lactobacillus observed in males. Lung transcriptomic analysis revealed immune-related gene expression changes involving B cell activation pathways. Serum metabolomics revealed significant decreases in ten metabolites across both sexes, identifying disruptions in amino acid and energy metabolism, with enrichment of the "Glycine, Serine, and Threonine Metabolism" KEGG pathway. Integrative network analyses revealed sex-specific correlations among immune genes, cytokines, and bile acid-related metabolites. These findings show that gradual extreme heat exposure triggers sex-specific systemic and pulmonary immunometabolic responses, offering insight into the biological effects of environmental heat stress and its potential health implications. HighlightsO_LIGradual heat exposure altered lung and serum cytokine profiles in mice C_LIO_LILactobacillus abundance decreased in males, despite stable microbial diversity C_LIO_LILung transcriptomics showed B cell-mediated immune activation after heat exposure C_LIO_LISerum metabolomics revealed heat-induced disruption of amino acid metabolism C_LIO_LIMulti-omics integration revealed sex-specific immunometabolic network responses C_LI

pharmacology and toxicology↗

Spatial transcriptomic profiling uncovers the molecular effects of the neurotoxicant polychlorinated biphenyls (PCBs) in the brains of adult mice

Environmental toxicants, such as polychlorinated biphenyls (PCBs), are highly stable synthetic organic compounds that are present in air, water, and soil. PCBs have been identified in post-mortem human brains of individuals with neurodegenerative diseases, indicating a possible link between environmental factors and disease risk. Research has revealed an association between PCB exposure and cognitive decline. Therefore, it is crucial to evaluate how PCB mixtures relevant to humans affect brain function and cognition. To investigate the effects of PCBs on memory and transcriptomic profiles, we exposed adult male C57BL/6J mice orally to a synthetic PCB mixture daily. After seven weeks of exposure, the mice were assessed in a spatial object recognition task (SOR) to evaluate long-term spatial memory. Our findings showed that mice exposed to PCBs exhibited deficits in long-term spatial memory. To examine the molecular effects of PCB on the brain, we used a spatial transcriptomics technique to analyze gene expression changes in five brain regions: the hippocampus, neocortex, thalamus, caudal putamen, and fiber tracts. Our analysis of spatial gene expression revealed the molecular signatures influenced by PCB in these susceptible brain regions of mice. Network analysis suggests that these changes are associated with higher chlorinated PCBs present in the brain. Additionally, we show that PCB exposure disrupts the expression of tight junction proteins, which are crucial for maintaining the integrity of the blood-brain barrier (BBB). Thus, our results offer mechanistic insights into how PCB exposure affects brain function and cognition.

neuroscience↗