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

Nat Commun. 2024 Jun 11;15(1):4773. doi: 10.1038/s41467-024-48625-2.

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.

MeSH terms

  • Adult
  • Female
  • Gene Expression Profiling
  • Humans
  • Inflammation* / genetics
  • Inflammation* / immunology
  • Inflammation* / metabolism
  • Male
  • Metagenomics / methods
  • Middle Aged
  • Multiomics
  • Proto-Oncogene Proteins p21(ras)* / genetics
  • Proto-Oncogene Proteins p21(ras)* / metabolism
  • Single-Cell Analysis
  • Skin* / immunology
  • Skin* / metabolism
  • Skin* / pathology
  • Space Flight*

Substances

  • Proto-Oncogene Proteins p21(ras)
  • KRAS protein, human