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

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This mouse study investigated how acute, gradual extreme heat exposure (an 8-hour ramp from 20°C to 38°C) affects systemic and pulmonary immune signaling and metabolic adaptations, using adult male and female C57Bl/6 mice assigned to heat-exposed, control, or pair-fed groups. Using multi-omics profiling (serum and lung cytokines, lung transcriptomics, cecal microbiome, and serum metabolomics), the authors found that heat significantly changed multiple cytokines in both lung and serum (including IL-17α, MIP-1α, MIP-1β, IL-1α, IL-12(p40), and RANTES), with lung transcriptomics showing immune-related alterations involving B cell activation pathways. Random forest and microbiome results identified taxa distinguishing groups, including a reduction in Lactobacillus in males, while metabolomics showed decreased serum metabolites enriched for glycine/serine/threonine metabolism and integrative analyses revealed sex-specific immune–metabolite correlations, including bile acid–related metabolites. The paper does not explicitly discuss any limitations in the provided text. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract 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°C to 38°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-17α, MIP-1α, MIP-1β, IL-1α, 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. Highlights Gradual heat exposure altered lung and serum cytokine profiles in mice Lactobacillus abundance decreased in males, despite stable microbial diversity Lung transcriptomics showed B cell–mediated immune activation after heat exposure Serum metabolomics revealed heat-induced disruption of amino acid metabolism Multi-omics integration revealed sex-specific immunometabolic network responses Competing Interest Statement The authors have declared no competing interest. Footnotes E-Mail Addresses: laura-gosse{at}uiowa.edu (L. E. Dean), andrea-a-dodd{at}uiowa.edu (A. Adamcakova-Dodd), and hans-joachim-lehmler{at}uiowa.edu (H. Lehmler)

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last seen: 2026-05-20T01:45:00.602351+00:00