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<p>Given NASA’s plans for manned lunar and Mars missions, it is critical to assess the risk of splenic immune dysregulation by using ground-based models of simulated microgravity (SMG) and/or chronic irradiation (CIR). To address this, C57BL/6 J mice of both sexes exposed to SMG and/or CIR for 29 days and alterations in immune cell distribution, function and phenotype were assessed. SMG and/or CIR altered a greater variety of immune cells in both lymphoid and myeloid lineages in female mice than in male mice; the function of splenic CD4 + T cells, CD8 + T cells, and CD19 + B cells altered in a sex-specific manner; and the distribution of different immune cells altered based on animal sex. These findings indicate that SMG and/or CIR alter the splenic immune cell distribution, phenotype and function in a sex-specific manner, underscoring the need for tailored strategies to mitigate health risks for crew members on long-term deep-space missions.</p>

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Sex-specific immune alterations in mice following long-term simulated microgravity and chronic irradiation

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年6月12日

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  • Edith Nathalie Pineda,
  • Bernice Nounamo,
  • Ruofei Du,
  • Enoch K. Larrey,
  • Cordell Gilreath,
  • Harrison Cook,
  • Marjan Boerma,
  • Igor Koturbash,
  • Rupak Pathak

摘要

Given NASA’s plans for manned lunar and Mars missions, it is critical to assess the risk of splenic immune dysregulation by using ground-based models of simulated microgravity (SMG) and/or chronic irradiation (CIR). To address this, C57BL/6 J mice of both sexes exposed to SMG and/or CIR for 29 days and alterations in immune cell distribution, function and phenotype were assessed. SMG and/or CIR altered a greater variety of immune cells in both lymphoid and myeloid lineages in female mice than in male mice; the function of splenic CD4 + T cells, CD8 + T cells, and CD19 + B cells altered in a sex-specific manner; and the distribution of different immune cells altered based on animal sex. These findings indicate that SMG and/or CIR alter the splenic immune cell distribution, phenotype and function in a sex-specific manner, underscoring the need for tailored strategies to mitigate health risks for crew members on long-term deep-space missions.