Radiobiology Unit, Institute for Nuclear Medical Applications, Belgian Nuclear Research Centre SCK CEN, Mol, Belgium.
Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.
Front Immunol. 2024 Sep 2;15:1443936. doi: 10.3389/fimmu.2024.1443936. eCollection 2024.
The immune system is an intricate network of cellular components that safeguards against pathogens and aberrant cells, with CD4+ T cells playing a central role in this process. Human space travel presents unique health challenges, such as heavy ion ionizing radiation, microgravity, and psychological stress, which can collectively impede immune function. The aim of this research was to examine the consequences of simulated space stressors on CD4+ T cell activation, cytokine production, and gene expression.
CD4+ T cells were obtained from healthy individuals and subjected to Fe ion particle radiation, Photon irradiation, simulated microgravity, and hydrocortisone, either individually or in different combinations. Cytokine levels for Th1 and Th2 cells were determined using multiplex Luminex assays, and RNA sequencing was used to investigate gene expression patterns and identify essential genes and pathways impacted by these stressors.
Simulated microgravity exposure resulted in an apparent Th1 to Th2 shift, evidenced on the level of cytokine secretion as well as altered gene expression. RNA sequencing analysis showed that several gene pathways were altered, particularly in response to Fe ions irradiation and simulated microgravity exposures. Individually, each space stressor caused differential gene expression, while the combination of stressors revealed complex interactions.
The research findings underscore the substantial influence of the space exposome on immune function, particularly in the regulation of T cell responses. Future work should focus expanding the limited knowledge in this field. Comprehending these modifications will be essential for devising effective strategies to safeguard the health of astronauts during extended space missions.
The effects of simulated space stressors on CD4+ T cell function are substantial, implying that space travel poses a potential threat to immune health. Additional research is necessary to investigate the intricate relationship between space stressors and to develop effective countermeasures to mitigate these consequences.
免疫系统是一个复杂的细胞成分网络,可抵御病原体和异常细胞,CD4+T 细胞在这一过程中起着核心作用。人类太空旅行带来了独特的健康挑战,如重离子电离辐射、微重力和心理压力,这些因素共同阻碍了免疫功能。本研究旨在研究模拟太空应激源对 CD4+T 细胞激活、细胞因子产生和基因表达的影响。
从健康个体中获得 CD4+T 细胞,并分别或组合接受 Fe 离子粒子辐射、光子照射、模拟微重力和氢化可的松处理。使用多重 Luminex 分析测定 Th1 和 Th2 细胞的细胞因子水平,使用 RNA 测序研究基因表达模式,并确定受这些应激源影响的关键基因和途径。
模拟微重力暴露导致明显的 Th1 向 Th2 转移,这在细胞因子分泌水平以及基因表达改变上均有体现。RNA 测序分析表明,几个基因途径发生了改变,特别是在对 Fe 离子辐射和模拟微重力暴露的反应中。单独的每个太空应激源都会导致不同的基因表达,而应激源的组合则显示出复杂的相互作用。
研究结果强调了太空暴露组对免疫功能的重大影响,特别是在 T 细胞反应的调节中。未来的工作应该集中在扩大这一领域的有限知识。理解这些变化对于制定保护宇航员在长期太空任务中健康的有效策略至关重要。
模拟太空应激源对 CD4+T 细胞功能的影响是巨大的,这表明太空旅行对免疫健康构成潜在威胁。需要进一步研究以调查太空应激源之间的复杂关系,并制定有效的对策来减轻这些后果。