Space Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Universities Space Research Association, Columbia, MD, United States.
Front Immunol. 2020 Nov 2;11:564950. doi: 10.3389/fimmu.2020.564950. eCollection 2020.
A comprehensive understanding of spaceflight factors involved in immune dysfunction and the evaluation of biomarkers to assess in-flight astronaut health are essential goals for NASA. An elevated neutrophil-to-lymphocyte ratio (NLR) is a potential biomarker candidate, as leukocyte differentials are altered during spaceflight. In the reduced gravity environment of space, rodents and astronauts displayed elevated NLR and granulocyte-to-lymphocyte ratios (GLR), respectively. To simulate microgravity using two well-established ground-based models, we cultured human whole blood-leukocytes in high-aspect rotating wall vessels (HARV-RWV) and used hindlimb unloaded (HU) mice. Both HARV-RWV simulation of leukocytes and HU-exposed mice showed elevated NLR profiles comparable to spaceflight exposed samples. To assess mechanisms involved, we found the simulated microgravity HARV-RWV model resulted in an imbalance of redox processes and activation of myeloperoxidase-producing inflammatory neutrophils, while antioxidant treatment reversed these effects. In the simulated microgravity HU model, mitochondrial catalase-transgenic mice that have reduced oxidative stress responses showed reduced neutrophil counts, NLR, and a dampened release of selective inflammatory cytokines compared to wildtype HU mice, suggesting simulated microgravity induced oxidative stress responses that triggered inflammation. In brief, both spaceflight and simulated microgravity models caused elevated NLR, indicating this as a potential biomarker for future in-flight immune health monitoring.
全面了解与免疫功能障碍相关的航天因素,以及评估用于评估飞行中宇航员健康的生物标志物,是美国宇航局的重要目标。中性粒细胞与淋巴细胞比值(NLR)升高是一个有潜力的生物标志物候选物,因为白细胞分类在航天飞行中会发生改变。在空间的微重力环境中,啮齿动物和宇航员的 NLR 和粒细胞与淋巴细胞比值(GLR)分别升高。为了使用两种成熟的地面模型模拟微重力,我们在高宽比旋转壁容器(HARV-RWV)中培养人全血白细胞,并使用后肢去负荷(HU)小鼠。HARV-RWV 模拟白细胞和 HU 暴露的小鼠均显示 NLR 谱升高,与航天暴露的样本相当。为了评估涉及的机制,我们发现模拟微重力的 HARV-RWV 模型导致氧化还原过程失衡和髓过氧化物酶产生的炎症性中性粒细胞激活,而抗氧化剂治疗逆转了这些效应。在模拟微重力的 HU 模型中,具有降低氧化应激反应的线粒体过氧化氢酶转基因小鼠与野生型 HU 小鼠相比,中性粒细胞计数、NLR 降低,选择性炎症细胞因子的释放减弱,表明模拟微重力引起的氧化应激反应引发了炎症。总之,航天飞行和模拟微重力模型都导致 NLR 升高,表明这是未来飞行中免疫健康监测的一个潜在生物标志物。