Department of Medical Biochemistry, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Integrative Genomics, Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Commun Biol. 2020 Sep 8;3(1):496. doi: 10.1038/s42003-020-01227-2.
Space flight produces an extreme environment with unique stressors, but little is known about how our body responds to these stresses. While there are many intractable limitations for in-flight space research, some can be overcome by utilizing gene knockout-disease model mice. Here, we report how deletion of Nrf2, a master regulator of stress defense pathways, affects the health of mice transported for a stay in the International Space Station (ISS). After 31 days in the ISS, all flight mice returned safely to Earth. Transcriptome and metabolome analyses revealed that the stresses of space travel evoked ageing-like changes of plasma metabolites and activated the Nrf2 signaling pathway. Especially, Nrf2 was found to be important for maintaining homeostasis of white adipose tissues. This study opens approaches for future space research utilizing murine gene knockout-disease models, and provides insights into mitigating space-induced stresses that limit the further exploration of space by humans.
太空飞行产生了一个具有独特压力源的极端环境,但我们对身体如何应对这些压力知之甚少。虽然在飞行中的太空研究有许多难以克服的限制,但利用基因敲除疾病模型小鼠可以克服其中一些限制。在这里,我们报告了 Nrf2(应激防御途径的主要调节因子)的缺失如何影响被送往国际空间站(ISS)停留的小鼠的健康。ISS 上 31 天后,所有飞行小鼠都安全返回地球。转录组和代谢组分析表明,太空旅行的压力引起了血浆代谢物的类似衰老的变化,并激活了 Nrf2 信号通路。特别是,发现 Nrf2 对于维持白色脂肪组织的内稳态很重要。这项研究为未来利用鼠基因敲除疾病模型进行太空研究开辟了途径,并为减轻限制人类进一步探索太空的太空诱导压力提供了思路。