Sexual dimorphism during integrative endocrine and immune responses to ionizing radiation in mice.
Marissa BurkeKelly WongYuli TalyanskySiddhita D MhatreCarol MitchellCassandra M JuranMakaila OlsonJanani IyerStephanie PuukilaCandice G T TahimicLane K ChristensonMoniece LoweLinda RubinsteinYasaman Shirazi-FardMarianne B SowaJoshua S AlwoodApril E RoncaAmber M PaulPublished in: Scientific reports (2024)
Exposure to cosmic ionizing radiation is an innate risk of the spaceflight environment that can cause DNA damage and altered cellular function. In astronauts, longitudinal monitoring of physiological systems and interactions between these systems are important to consider for mitigation strategies. In addition, assessments of sex-specific biological responses in the unique environment of spaceflight are vital to support future exploration missions that include both females and males. Here we assessed sex-specific, multi-system immune and endocrine responses to simulated cosmic radiation. For this, 24-week-old, male and female C57Bl/6J mice were exposed to simplified five-ion, space-relevant galactic cosmic ray (GCRsim) radiation at 15 and 50 cGy, to simulate predicted radiation exposures that would be experienced during lunar and Martian missions, respectively. Blood and adrenal tissues were collected at 3- and 14-days post-irradiation for analysis of immune and endocrine biosignatures and pathways. Sexually dimorphic adrenal gland weights and morphology, differential total RNA expression with corresponding gene ontology, and unique immune phenotypes were altered by GCRsim. In brief, this study offers new insights into sexually dimorphic immune and endocrine kinetics following simulated cosmic radiation exposure and highlights the necessity for personalized translational approaches for astronauts during exploration missions.
Keyphrases
- immune response
- dna damage
- oxidative stress
- radiation induced
- high fat diet induced
- poor prognosis
- mental health
- air pollution
- clinical trial
- randomized controlled trial
- insulin resistance
- genome wide
- dendritic cells
- toll like receptor
- skeletal muscle
- copy number
- current status
- network analysis
- study protocol
- genome wide analysis