Genome and clonal hematopoiesis stability contrasts with immune, cfDNA, mitochondrial, and telomere length changes during short duration spaceflight
J. Sebastian Garcia-Medina , Karolina Sienkiewicz , S. Anand Narayanan , Eliah G. Overbey , Kirill Grigorev , Krista A. Ryon , Marissa Burke , Jacqueline Proszynski , Braden Tierney , Caleb M. Schmidt , Nuria Mencia-Trinchant , Remi Klotz , Veronica Ortiz , Jonathan Foox , Christopher Chin , Deena Najjar , Irina Matei , Irenaeus Chan , Carlos Cruchaga , Ashley Kleinman , JangKeun Kim , Alexander Lucaci , Conor Loy , Omary Mzava , Iwijn De Vlaminck , Anvita Singaraju , Lynn E. Taylor , Julian C. Schmidt , Michael A. Schmidt , Kelly Blease , Juan Moreno , Andrew Boddicker , Junhua Zhao , Bryan Lajoie , Andrew Altomare , Semyon Kruglyak , Shawn Levy , Min Yu , Duane C. Hassane , Susan M. Bailey , Kelly Bolton , Jaime Mateus , Christopher E. Mason
Precision Clinical Medicine ›› 2024, Vol. 7 ›› Issue (1) : pbad007
Genome and clonal hematopoiesis stability contrasts with immune, cfDNA, mitochondrial, and telomere length changes during short duration spaceflight
Background: The Inspiration4 (I4) mission, the first all-civilian orbital flight mission, investigated the physiological effects of short-duration spaceflight through a multi-omic approach. Despite advances, there remains much to learn about human adaptation to spaceflight's unique challenges, including microgravity, immune system perturbations, and radiation exposure.
Methods: To provide a detailed genetics analysis of the mission, we collected dried blood spots pre-, during, and post-flight for DNA extraction. Telomere length was measured by quantitative PCR, while whole genome and cfDNA sequencing provided insight into genomic stability and immune adaptations. A robust bioinformatic pipeline was used for data analysis, including variant calling to assess mutational burden.
Result: Telomere elongation occurred during spaceflight and shortened after return to Earth. Cell-free DNA analysis revealed increased immune cell signatures post-flight. No significant clonal hematopoiesis of indeterminate potential (CHIP) or whole-genome instability was observed. The long-term gene expression changes across immune cells suggested cellular adaptations to the space environment persisting months post-flight.
Conclusion: Our findings provide valuable insights into the physiological consequences of short-duration spaceflight, with telomere dynamics and immune cell gene expression adapting to spaceflight and persisting after return to Earth. CHIP sequencing data will serve as a reference point for studying the early development of CHIP in astronauts, an understudied phenomenon as previous studies have focused on career astronauts. This study will serve as a reference point for future commercial and non-commercial spaceflight, low Earth orbit (LEO) missions, and deep-space exploration.
genomes / clonal / hematopoiesis / stability / immune / mitochondria / ribosomes / spaceflight
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