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Review
. 2024 Jun 11;10(1):63.
doi: 10.1038/s41526-023-00293-0.

Influence of the spaceflight environment on macrophage lineages

Affiliations
Review

Influence of the spaceflight environment on macrophage lineages

Rocky An et al. NPJ Microgravity. .

Abstract

Spaceflight and terrestrial spaceflight analogs can alter immune phenotypes. Macrophages are important immune cells that bridge the innate and adaptive immune systems and participate in immunoregulatory processes of homeostasis. Furthermore, macrophages are critically involved in initiating immunity, defending against injury and infection, and are also involved in immune resolution and wound healing. Heterogeneous populations of macrophage-type cells reside in many tissues and cause a variety of tissue-specific effects through direct or indirect interactions with other physiological systems, including the nervous and endocrine systems. It is vital to understand how macrophages respond to the unique environment of space to safeguard crew members with appropriate countermeasures for future missions in low Earth orbit and beyond. This review highlights current literature on macrophage responses to spaceflight and spaceflight analogs.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. In-Flight Macrophage Lineage Phenotypes.
Representative timeline of the observable phenotypes produced in-flight from Table 1. Each line/color represents a mission experiment with the in-flight days listed above/below vertical nodes. Collective observable phenotypes display increased (above centerline) or decreased (below centerline) activity are depicted visually, including increased production of IL12-p40, CXCL-8, CXCL-5, TNF-α, IL-1β, IL-RA, IL-1α, IL-17F, and IL-6 and decreased macrophage differentiation processes from hematopoietic progenitor cells (HPC). Created with BioRender.com.
Fig. 2
Fig. 2. Post-Flight Macrophage Lineage Phenotypes.
Representative timeline of the observable phenotypes produced post-flight analysis from Table 1. Each line/color represents a mission experiment with the in-flight days listed above horizontal nodes, and post-flight collection time points vertical lines. Collective observable phenotypes that display increased (above centerline) or decreased (below centerline) activity are depicted visually, including monocytic count, phagocytic function, cytokine production, and T cell tolerance outcomes. Each phenotype is color-coordinated with the experimental timeline of missions and collections. Created with BioRender.com.

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References

    1. Afshinnekoo E, et al. Fundamental Biological Features of Spaceflight: Advancing the Field to Enable Deep-Space Exploration. Cell. 2020;183:1162–1184. doi: 10.1016/j.cell.2020.10.050. - DOI - PMC - PubMed
    1. Garrett-Bakelman, F. E. et al. The NASA Twins Study: A multidimensional analysis of a year-long human spaceflight. Science364, aau8650 (2019). - PMC - PubMed
    1. Paul AM, et al. Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice. iScience. 2020;23:101747. doi: 10.1016/j.isci.2020.101747. - DOI - PMC - PubMed
    1. Malkani S, et al. Circulating miRNA Spaceflight Signature Reveals Targets for Countermeasure Development. Cell Rep. 2020;33:108448. doi: 10.1016/j.celrep.2020.108448. - DOI - PMC - PubMed
    1. Crucian BE, et al. Plasma cytokine concentrations indicate that in vivo hormonal regulation of immunity is altered during long-duration spaceflight. J. Interferon. Cytokine Res. 2014;34:778–786. doi: 10.1089/jir.2013.0129. - DOI - PMC - PubMed