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Single-cell multi-ome and immune profiles of the Inspiration4 crew reveal conserved, cell-type, and sex-specific responses to spaceflight.

Authors :
Kim J
Tierney BT
Overbey EG
Dantas E
Fuentealba M
Park J
Narayanan SA
Wu F
Najjar D
Chin CR
Meydan C
Loy C
Mathyk B
Klotz R
Ortiz V
Nguyen K
Ryon KA
Damle N
Houerbi N
Patras LI
Schanzer N
Hutchinson GA
Foox J
Bhattacharya C
Mackay M
Afshin EE
Hirschberg JW
Kleinman AS
Schmidt JC
Schmidt CM
Schmidt MA
Beheshti A
Matei I
Lyden D
Mullane S
Asadi A
Lenz JS
Mzava O
Yu M
Ganesan S
De Vlaminck I
Melnick AM
Barisic D
Winer DA
Zwart SR
Crucian BE
Smith SM
Mateus J
Furman D
Mason CE
Source :
Nature communications [Nat Commun] 2024 Jun 11; Vol. 15 (1), pp. 4954. Date of Electronic Publication: 2024 Jun 11.
Publication Year :
2024

Abstract

Spaceflight induces an immune response in astronauts. To better characterize this effect, we generated single-cell, multi-ome, cell-free RNA (cfRNA), biochemical, and hematology data for the SpaceX Inspiration4 (I4) mission crew. We found that 18 cytokines/chemokines related to inflammation, aging, and muscle homeostasis changed after spaceflight. In I4 single-cell multi-omics data, we identified a "spaceflight signature" of gene expression characterized by enrichment in oxidative phosphorylation, UV response, immune function, and TCF21 pathways. We confirmed the presence of this signature in independent datasets, including the NASA Twins Study, the I4 skin spatial transcriptomics, and 817 NASA GeneLab mouse transcriptomes. Finally, we observed that (1) T cells showed an up-regulation of FOXP3, (2) MHC class I genes exhibited long-term suppression, and (3) infection-related immune pathways were associated with microbiome shifts. In summary, this study reveals conserved and distinct immune disruptions occurring and details a roadmap for potential countermeasures to preserve astronaut health.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
38862516
Full Text :
https://doi.org/10.1038/s41467-024-49211-2