Cells (Oct 2023)

Spaceflight Induces Strength Decline in <i>Caenorhabditis elegans</i>

  • Purushottam Soni,
  • Hunter Edwards,
  • Taslim Anupom,
  • Mizanur Rahman,
  • Leila Lesanpezeshki,
  • Jerzy Blawzdziewicz,
  • Henry Cope,
  • Nima Gharahdaghi,
  • Daniel Scott,
  • Li Shean Toh,
  • Philip M. Williams,
  • Timothy Etheridge,
  • Nathaniel Szewczyk,
  • Craig R. G. Willis,
  • Siva A. Vanapalli

DOI
https://doi.org/10.3390/cells12202470
Journal volume & issue
Vol. 12, no. 20
p. 2470

Abstract

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Background: Understanding and countering the well-established negative health consequences of spaceflight remains a primary challenge preventing safe deep space exploration. Targeted/personalized therapeutics are at the forefront of space medicine strategies, and cross-species molecular signatures now define the ‘typical’ spaceflight response. However, a lack of direct genotype–phenotype associations currently limits the robustness and, therefore, the therapeutic utility of putative mechanisms underpinning pathological changes in flight. Methods: We employed the worm Caenorhabditis elegans as a validated model of space biology, combined with ‘NemaFlex-S’ microfluidic devices for assessing animal strength production as one of the most reproducible physiological responses to spaceflight. Wild-type and dys-1 (BZ33) strains (a Duchenne muscular dystrophy (DMD) model for comparing predisposed muscle weak animals) were cultured on the International Space Station in chemically defined media before loading second-generation gravid adults into NemaFlex-S devices to assess individual animal strength. These same cultures were then frozen on orbit before returning to Earth for next-generation sequencing transcriptomic analysis. Results: Neuromuscular strength was lower in flight versus ground controls (16.6% decline, p dys-1 significantly more (23% less strength, p dys-1 animals in flight again cluster to neuronal/neuromuscular pathways, suggesting strength loss in DMD comprises a strong neuronal component that predisposes these animals to exacerbated strength loss in space. Conclusions: Highly reproducible gene signatures are strongly associated with space-induced neuromuscular strength loss across species and neuronal changes in calcium/acetylcholine signaling require further study. These results promote targeted medical efforts towards and provide an in vivo model for safely sending animals and people into deep space in the near future.

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