Nature Communications (Jun 2024)

Spatial multi-omics of human skin reveals KRAS and inflammatory responses to spaceflight

  • Jiwoon Park,
  • Eliah G. Overbey,
  • S. Anand Narayanan,
  • JangKeun Kim,
  • Braden T. Tierney,
  • Namita Damle,
  • Deena Najjar,
  • Krista A. Ryon,
  • Jacqueline Proszynski,
  • Ashley Kleinman,
  • Jeremy Wain Hirschberg,
  • Matthew MacKay,
  • Evan E. Afshin,
  • Richard Granstein,
  • Justin Gurvitch,
  • Briana M. Hudson,
  • Aric Rininger,
  • Sean Mullane,
  • Sarah E. Church,
  • Cem Meydan,
  • George Church,
  • Afshin Beheshti,
  • Jaime Mateus,
  • Christopher E. Mason

DOI
https://doi.org/10.1038/s41467-024-48625-2
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 14

Abstract

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Abstract Spaceflight can change metabolic, immunological, and biological homeostasis and cause skin rashes and irritation, yet the molecular basis remains unclear. To investigate the impact of short-duration spaceflight on the skin, we conducted skin biopsies on the Inspiration4 crew members before (L-44) and after (R + 1) flight. Leveraging multi-omics assays including GeoMx™ Digital Spatial Profiler, single-cell RNA/ATAC-seq, and metagenomics/metatranscriptomics, we assessed spatial gene expressions and associated microbial and immune changes across 95 skin regions in four compartments: outer epidermis, inner epidermis, outer dermis, and vasculature. Post-flight samples showed significant up-regulation of genes related to inflammation and KRAS signaling across all skin regions. These spaceflight-associated changes mapped to specific cellular responses, including altered interferon responses, DNA damage, epithelial barrier disruptions, T-cell migration, and hindered regeneration were located primarily in outer tissue compartments. We also linked epithelial disruption to microbial shifts in skin swab and immune cell activity to PBMC single-cell data from the same crew and timepoints. Our findings present the inaugural collection and examination of astronaut skin, offering insights for future space missions and response countermeasures.