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Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice

机译:除了低地轨道之外:在模拟小鼠中模拟深空性条件后表征免疫和microRNA差异

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摘要

Spaceflight missions can cause immune system dysfunction in astronauts with little understanding of immune outcomes in deep space. This study assessed immune responses in mice following ground-based, simulated deep spaceflight conditions, compared with data from astronauts on International Space Station missions. For ground studies, we simulated microgravity using the hindlimb unloaded mouse model alone or in combination with acute simulated galactic cosmic rays or solar particle events irradiation. Immune profiling results revealed unique immune diversity following each experimental condition, suggesting each stressor results in distinct circulating immune responses, with clear consequences for deep spaceflight. Circulating plasma microRNA sequence analysis revealed involvement in immune system dysregulation. Furthermore, a large astronaut cohort showed elevated inflammation during low-Earth orbit missions, thereby supporting our simulated ground experiments in mice. Herein, circulating immune biomarkers are defined by distinct deep space irradiation types coupled to simulated microgravity and could be targets for future space health initiatives.
机译:宇航员可能导致宇航员的免疫系统功能障碍,很少了解深层空间中的免疫结果。该研究与来自国际空间站任务的宇航员的数据相比,在基于地面的模拟的深空条件下评估了小鼠的免疫应答。对于地面研究,我们使用Hindlimb卸载小鼠模型或与急性模拟的银宇宙射线或太阳粒子事件辐射组合模拟微匍匐性。免疫分析结果显示每种实验条件后的独特免疫多样性,表明每个压力源导致不同的循环免疫反应,具有清晰的水污染后果。循环等离子体MicroRNA序列分析显示涉及免疫系统的丧失抑制。此外,大宇航员队列在低地轨道任务期间显示出炎症升高,从而支持小鼠的模拟地面实验。在此,循环免疫生物标志物由耦合到模拟微争的不同的深空辐射类型来定义,并且可能是未来空间健康倡议的目标。

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