Human immune system adaptations to simulated microgravity revealed by single-cell mass cytometry.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
07 06 2021
Historique:
received: 17 02 2021
accepted: 11 05 2021
entrez: 8 6 2021
pubmed: 9 6 2021
medline: 9 11 2021
Statut: epublish

Résumé

Exposure to microgravity (µG) during space flights produces a state of immunosuppression, leading to increased viral shedding, which could interfere with long term missions. However, the cellular mechanisms that underlie the immunosuppressive effects of µG are ill-defined. A deep understanding of human immune adaptations to µG is a necessary first step to design data-driven interventions aimed at preserving astronauts' immune defense during short- and long-term spaceflights. We employed a high-dimensional mass cytometry approach to characterize over 250 cell-specific functional responses in 18 innate and adaptive immune cell subsets exposed to 1G or simulated (s)µG using the Rotating Wall Vessel. A statistically stringent elastic net method produced a multivariate model that accurately stratified immune responses observed in 1G and sµG (p value 2E-4, cross-validation). Aspects of our analysis resonated with prior knowledge of human immune adaptations to µG, including the dampening of Natural Killer, CD4

Identifiants

pubmed: 34099760
doi: 10.1038/s41598-021-90458-2
pii: 10.1038/s41598-021-90458-2
pmc: PMC8184772
doi:

Substances chimiques

RNA, Messenger 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

11872

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM137936
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM138353
Pays : United States

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Auteurs

J M Spatz (JM)

Department of Medicine, Metabolism Division, San Francisco Department of Veterans Affairs Medical Center, San Francisco, CA, USA.
Department of Medicine and Department of Surgery, University of California, San Francisco, CA, USA.

M Hughes Fulford (MH)

Department of Medicine, Metabolism Division, San Francisco Department of Veterans Affairs Medical Center, San Francisco, CA, USA.
Department of Medicine and Department of Surgery, University of California, San Francisco, CA, USA.

A Tsai (A)

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, 300 Pasteur Dr. Rm S238, Grant Bldg, Stanford, CA, 94305, USA.

D Gaudilliere (D)

Department of Surgery, Plastic Surgery Division, Stanford University School of Medicine, Stanford, CA, 94305, USA.

J Hedou (J)

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, 300 Pasteur Dr. Rm S238, Grant Bldg, Stanford, CA, 94305, USA.

E Ganio (E)

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, 300 Pasteur Dr. Rm S238, Grant Bldg, Stanford, CA, 94305, USA.

M Angst (M)

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, 300 Pasteur Dr. Rm S238, Grant Bldg, Stanford, CA, 94305, USA.

N Aghaeepour (N)

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, 300 Pasteur Dr. Rm S238, Grant Bldg, Stanford, CA, 94305, USA.
Department of Biomedical Data Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.

Brice Gaudilliere (B)

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, 300 Pasteur Dr. Rm S238, Grant Bldg, Stanford, CA, 94305, USA. gbrice@stanford.edu.

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Classifications MeSH