Taylor Katherine, Kleinhesselink Kurt, George Michael D, Morgan Rachel, Smallwood Tangi, Hammonds Ann S, Fuller Patrick M, Saelao Perot, Alley Jeff, Gibbs Allen G, Hoshizaki Deborah K, von Kalm Laurence, Fuller Charles A, Beckingham Kathleen M, Kimbrell Deborah A
Department of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.
Department of Medical Microbiology and Immunology, University of California Davis, Davis, California, United States of America.
PLoS One. 2014 Jan 24;9(1):e86485. doi: 10.1371/journal.pone.0086485. eCollection 2014.
Space travel presents unlimited opportunities for exploration and discovery, but requires better understanding of the biological consequences of long-term exposure to spaceflight. Immune function in particular is relevant for space travel. Human immune responses are weakened in space, with increased vulnerability to opportunistic infections and immune-related conditions. In addition, microorganisms can become more virulent in space, causing further challenges to health. To understand these issues better and to contribute to design of effective countermeasures, we used the Drosophila model of innate immunity to study immune responses in both hypergravity and spaceflight. Focusing on infections mediated through the conserved Toll and Imd signaling pathways, we found that hypergravity improves resistance to Toll-mediated fungal infections except in a known gravitaxis mutant of the yuri gagarin gene. These results led to the first spaceflight project on Drosophila immunity, in which flies that developed to adulthood in microgravity were assessed for immune responses by transcription profiling on return to Earth. Spaceflight alone altered transcription, producing activation of the heat shock stress system. Space flies subsequently infected by fungus failed to activate the Toll pathway. In contrast, bacterial infection produced normal activation of the Imd pathway. We speculate on possible linkage between functional Toll signaling and the heat shock chaperone system. Our major findings are that hypergravity and spaceflight have opposing effects, and that spaceflight produces stress-related transcriptional responses and results in a specific inability to mount a Toll-mediated infection response.
太空旅行提供了无限的探索和发现机会,但需要更好地了解长期暴露于太空飞行的生物学后果。免疫功能尤其与太空旅行相关。人类的免疫反应在太空中会减弱,更容易受到机会性感染和免疫相关疾病的影响。此外,微生物在太空中可能会变得更具毒性,对健康造成进一步挑战。为了更好地理解这些问题并为设计有效的应对措施做出贡献,我们利用果蝇先天免疫模型研究了超重力和太空飞行中的免疫反应。聚焦于通过保守的Toll和Imd信号通路介导的感染,我们发现除了尤里·加加林基因的一个已知趋地性突变体之外,超重力可提高对Toll介导的真菌感染的抵抗力。这些结果促成了首个关于果蝇免疫的太空飞行项目,在该项目中,在微重力环境下发育至成年的果蝇在返回地球后通过转录谱分析来评估其免疫反应。仅太空飞行就改变了转录,激活了热休克应激系统。随后被真菌感染的太空果蝇未能激活Toll通路。相比之下,细菌感染则使Imd通路正常激活。我们推测了功能性Toll信号与热休克伴侣系统之间可能的联系。我们的主要发现是,超重力和太空飞行具有相反的作用,太空飞行会产生与应激相关的转录反应,并导致无法产生特定的Toll介导的感染反应。