<p>Ontological analysis of CHIP gene variants.</p>

A series of secondary endpoints were also measured. Sham irradiation with HLU increased blood lymphocytes but not myeloid cells compared with non-HLU, an outcome that was inhibited by simGCRsim with HLU, indicating an interaction between spaceflight stressors at this high dose-rate. HLU alone decreased multiple circulating cytokines and depleted CD56⁺ cells in the spleen.

Notably, simGCRsim and HLU alone and in combination did not disrupt calcium homeostasis. An exposure to 1.5 Gy simGCRsim no HLU revealed distinct genomic alterations in circulating nucleated blood cells as compared with sham-irradiated subjects no HLU, and identified mutations, frameshifts, and deletions in genes that contribute to human disease in the irradiated cohort. A limited follow-on study involved exposure to 0.75 Gy simGCRsim with no HLU with appropriate controls.

This radiation dose, a dose relevant to human missions to Mars, caused cardiac perivascular fibrosis at an extended follow up period of after 360 days. Taken together, our findings show exposure to simGCRsim, representing the composition of GCR behind spacecraft shielding, caused cardiac perivascular fibrosis and gene variants. Simulated microgravity (HLU) alone engaged the immune system and decreased cytokine production.

We conclude that exposure of rats to simGCRsim and/or HLU results in persistent health effects with limited interactions between the two spaceflight stressors.</p></div>