# Effects of Space Flight on Inflammasome Activation in the Brain of Mice

**Authors:** Upal Roy, Roey Hadad, Angel A. Rodriguez, Alen Saju, Deepa Roy, Mario Gil, Robert W. Keane, Ryan T. Scott, Xiao W. Mao, Juan Pablo de Rivero Vaccari

PMC · DOI: 10.3390/cells14060417 · Cells · 2025-03-12

## TL;DR

This study shows that spaceflight reduces inflammasome activation in the brains of mice, suggesting a weakened innate immune response in space.

## Contribution

The study provides new evidence on how spaceflight affects innate immune signaling in the brain of mice.

## Key findings

- Spaceflight led to decreased inflammasome activation in mouse brains compared to ground controls.
- No significant changes were observed in pro-inflammatory cytokine levels between flight and ground groups.

## Abstract

Space flight exposes astronauts to stressors that alter the immune response, rendering them vulnerable to infections and diseases. In this study, we aimed to determine the levels of inflammasome activation in the brains of mice that were housed in the International Space Station (ISS) for 37 days. C57BL/6 mice were launched to the ISS as part of NASA’s Rodent Research 1 Mission on SpaceX-4 CRS-4 Dragon cargo spacecraft from 21 September 2014 to 25 October 2014. Dissected mouse brains from that mission were analyzed by immunoblotting of inflammasome signaling proteins and Electrochemiluminescence Immunoassay (ECLIA) for inflammatory cytokine levels. Our data indicate decreased inflammasome activation in the brains of mice that were housed in the ISS for 37 days when compared to the brains of mice that were maintained on the ground, and in mice corresponding to the baseline group that were sacrificed at the time of launching of SpaceX-4. Moreover, we did not detect any significant changes in the expression levels of the pro-inflammatory cytokines TNF-α, IL-2, IFN-γ, IL-5, IL-6, IL-12p70 and IL-10 between the ground control and the flight groups. Together, these studies suggest that spaceflight results in a decrease in the levels of innate immune signaling molecules that govern inflammasome signaling in the brain of mice.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL2 (interleukin 2), IFNG (interferon gamma), IL5 (interleukin 5), IL6 (interleukin 6), IL10 (interleukin 10)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Il2 (interleukin 2) [NCBI Gene 16183] {aka Il-2}, Il5 (interleukin 5) [NCBI Gene 16191] {aka Il-5}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** infections (MESH:D007239), inflammatory (MESH:D007249)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11941215/full.md

## References

99 references — full list in the complete paper: https://tomesphere.com/paper/PMC11941215/full.md

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Source: https://tomesphere.com/paper/PMC11941215