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Strategies for Study of Neuroprotection from Cold-preconditioning
Published on: September 2, 2010
Transcriptomic Profiling Reveals Immunometabolic Gene Regulation during a 24-Hour Cold Exposure Survival Simulation
Jing Zhang1, Shawn G Rhind1,2, Michel B Ducharme3,4
1Defense Research and Development Canada, Toronto Research Centre, Toronto, Ontario, Canada.
None:
Prolonged cold exposure imposes substantial physiological and operational demands; however, the molecular mechanisms supporting human adaptation to sustained cold remain poorly defined. In this first-in-human study, we conducted genome-wide transcriptomic profiling of peripheral blood leukocytes from eight healthy adult males during a 24-h whole-body cold survival simulation (7.5 °C). Blood samples were collected at four standardized time points to characterize the dynamics of gene expression during continuous cold stress. Despite the clear physiological strain, the global leukocyte transcriptome remained remarkably stable. Differential expression analyses revealed a focused, transient induction of immediate-early genes-including FOS, TAGAP, and TIPARP-primarily associated with standardized exercise bouts performed immediately before and after cold exposure, with expression returning to baseline thereafter. KEGG pathway enrichment indicated activation of immune and stress response signaling pathways (e.g., Toll-like receptor, MAPK, and B-cell receptor signaling) following pre-cold exercise, whereas post-cold sampling was enriched for metabolic pathways, including oxidative phosphorylation and glycolysis/gluconeogenesis, consistent with sustained thermogenic demand and metabolic flexibility. Notably, prolonged cold exposure was not associated with broad inflammatory activation, suggesting that humans maintain transcriptomic homeostasis under sustained cold stress through targeted, energetically efficient immunometabolic regulation. These findings establish peripheral blood as a viable biosampling matrix for monitoring gene-environment interactions during prolonged cold exposure and demonstrate the feasibility of transcriptomic surveillance in extreme environments. Collectively, this study provides foundational systems-level insights into early molecular signatures of human cold resilience and informs the development of blood-based biomarkers, predictive models, and precision countermeasures to support health and performance in Arctic, military, and expeditionary settings.

