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Guest Edited Collection: Gravitational biology and space medicine

A Publisher Correction to this article was published on 19 November 2019

This article has been updated

A return to the Moon, Mars expeditions, and a rise in space tourism will lead to an increasing number of human spaceflights. The ‘Gravitational biology and space medicine’ Collection focuses on the challenges to the health of humans in space during long-term space missions and the physiological changes during short-term altered gravity conditions, the possible influence of space radiation, available countermeasures and possible applications on Earth. In addition, studies reporting on in vivo changes in space-flown mice were published. Finally, this Collection also brings together articles reporting experiments using cells cultured under conditions of real microgravity on the International Space Station, or exposed in ground-based facilities, in order to study morphological and molecular alterations in different cell types.

Experiencing a spaceflight is a dream of many enthusiasts and those working in space research. However, while a space journey is fascinating, unfortunately, it can cause various short- and long-term health concerns. Human and animal bodies undergo dramatic changes after an extended stay on the International Space Station (ISS)1,2.

Space medicine deals with the physiological and biological effects of spaceflight on the human organism, its organs, tissues and cells1,3,4,5. It includes administering medicine to astronauts, cosmonauts, taikonauts and private space travellers in outer space and on Earth, along with the development of countermeasures for the various health problems of humans in space.

For medical and biotechnological reasons, it is important to study animals and mammalian cells that are exposed to real microgravity (r-µg) in space. It is necessary to detect the cellular changes responsible for the various medical problems often observed in humans on the ISS. The cellular response to microgravity (µg) has been partially described for humans and animal models, whereas the intracellular regulatory mechanisms are still a mystery. Studies on whole organisms, cells and tissues are not only complementary but essential for a holistic interpretation. In such models, several molecular mechanisms involved in biological processes have been characterised3,4,5,6.

Studies of tissues and cells exposed to r-µg are rare and rather costly. For this reason, researchers have developed simulation devices to generate µg on Earth, such as the NASA-developed rotating wall vessel (RWV) bioreactor, the random positioning machine (RPM), the magnetic levitator, and the two- (2D) and three-dimensional (3D) clinostats, to prepare for spaceflights and to perform ground-based µg experiments on stem and other specialised cells7,8,9,10. In addition, the National Aeronautics and Space Administration (NASA), the European Space Agency (ESA) and other agencies offer the possibility of short-term µg experiences, such as parabolic flight (PF)11,12,13 and sounding rocket missions12.

The Guest Edited Collection ‘Gravitational biology and space medicine’ includes publications reporting on health concerns for astronauts and cosmonauts14,15,16 during space missions, and physiological changes caused by short-term µg17. Several studies investigating the impact of µg on the behaviour and health of mice on the ISS were published in this Collection18,19,20,21,22,23, in addition to investigations at the cellular level in space24 and in short-term µg provided by PF maneuvers25. Moreover, cell studies in simulated (s-) µg at ground-based facilities are included in this Collection26,27,28,29,30.

Humans in space can experience various health problems. Immunosuppression in spaceflight increases the risk of opportunistic infections. Crewmembers are exposed to different stressors, potentially altering the composition of their microbiomes. Voorhies et al.14 investigated nine astronauts, and showed that the composition of the astronauts’ microbiome (gastrointestinal tract, skin, nose and tongue) was changed during space travel. Notably, the altered skin microbiome might be involved in the frequently observed skin rashes and hypersensitivity episodes of astronauts. These findings warrant further detailed examination before deeper space exploration starts. Moore et al.15 demonstrated that long-duration spaceflight adversely affects post-landing operator proficiency. Eight crewmembers experienced general discomfort in motor function and motion perception after a mission, and a lack of cognitive reserve. This only manifested in duplicate tasks that recovered to baseline four days after landing15. These results suggest that the development of countermeasures should target the cumulative effect of the subtle physiological changes observed on landing day. Recommendations for countermeasures were published in Moore et al.15. Reynolds et al.16, investigated 301 astronauts and 117 cosmonauts, demonstrating that space radiation has no strong impact on their mortality. They showed that survival estimates from Kaplan-Meier curves were largely congruent with those of competing risk methods, suggesting that if ionising radiation impacts the risk of death due to cancer and cardiovascular disease, the effect is not dramatic16. However, the authors concluded that future deep space exploration might provide larger doses of space radiation, leading to a different risk profile for future astronauts and cosmonauts; therefore, it is important to continue their surveillance for potential harmful effects of such exposure16.

Investigations of the human stance during PF maneuvers compared to 1g-conditions revealed the similarity of postural recovery responses in 1g-, hypo- and hyper-gravity conditions17. These results showed that muscle synergies and segmental strategies acquired on Earth are robust and persistent across variable acute changes in gravitation17.

The NASA Rodent Habitat on the ISS was used to study the behaviour of mice in r-µg, and for investigating changes in different tissues18,19,20,21,22,23. The detailed behavioural analysis of these mice provides a useful model system for increasing our knowledge of human responses to spaceflight18. These studies provide the opportunity to examine how physical movement influences responses to µg18.

Ogneva et al.19 studied the vas deferens and testes tissues of space-flown mice. They found that during the 3-week spaceflight an adaptive protein profile formed in the germinative tissue of male mice19. In addition, gene expression of Tet2 demethylase was increased and histone deacetylase (Hdac1) decreased19. The mRNA expression changes might be important during the early period of readaptation, since they could lead to an increase in the expression of target genes19.

Spaceflight is associated with loss of muscle mass and strength1. Cadena et al.20 investigated E3 ubiquitin ligase MuRF1 (Muscle-specific RING finger 1) null KO mice in space on the ISS and by the hindlimb suspension model. The muscle of MuRF1 null mice was protected in the ground-based model. By contrast, skeletal muscle atrophy in these mice was enhanced by unique mechanisms in space20.

Another important health concern for crewmembers is spaceflight-induced structural and functional damage of the eyes. Mao et al. investigated mice on the ISS21. They demonstrated blood-retinal barrier (BRB) disruption and ocular adaptation after the 35-day mission. Post-flight proteomics studies revealed changes in cell death (apoptosis), cell cycle, immune responses, mitochondrial function and metabolic stress in space-flown mice compared to ground-based control animals21. The results of this study show a complex cellular response influencing the structure of the retina and BRB integrity after the 35-day space mission21. A second study assessing eye changes after spaceflight identified 600 differentially expressed genes by RNA sequencing in mouse retinas22. The differentially expressed genes were associated with retinitis pigmentosa and changes in chromatin structure. In addition, the thicknesses of the retina, the retinal pigment epithelium and the choroid layer were lower after spaceflight, indicating that retinal changes cause the visual problems22. Finally, whole-transcript cDNA sequencing showed that a 35-day stay in orbit on ISS may alter the homeostatic gene expression of mice spleens by a combination of µg and other environmental stressors23.

The Collection also covers cell and molecular biological studies in space, and for short-term µg episodes provided by PFs. Gambacurta et al.24 showed that rapamycin induces transcriptional activation of human blood-derived stem cells (BDSCs) towards osteogenic differentiation in space. These findings, applying proteomics and epigenetic methods, may represent the first step in identifying new biomarkers and therapeutic targets to treat osteoporosis in space and on Earth24.

A PF study examined the attachment of peripheral blood mononuclear cells to adhesion molecules under flow conditions, and antigen-induced immune activation in whole blood25. The flow and rolling speed of cells were moderately accelerated during µg periods, which were accompanied by a clear reduction in rolling rate. After the PF, whole blood tests indicated monocytes were in a “primed” state, with potentiated antigen-induced pro-inflammatory cytokine responses. In addition, anti-inflammatory cytokines were elevated, and monocytes showed a surface molecule pattern indicating immunosuppression. The results suggest an immunologic counterbalance to avoid disproportionate immune responses.

3D clinorotation was used to study mesenchymal stromal cell (MSC) response to inflammatory stimulation26. A reduced response of MSCs to priming in µg might also indicate less involvement of these cells in tissue remodelling26. Arun et al.27 studied the effects of s-µg on increasing stemness in human colorectal cancer cells (HCT116), using a rotary cell culture system (RCCS). This study highlighted the importance of µg and physical factors in the regulation of stemness in colorectal cancer cells27. Cancer research in space is currently a popular area of study29, with the prospect of researchers developing new cancer treatment strategies. Notably, Costantini et al.28 showed that RCCS-exposure promoted cells to form 3D spheroids. It also stimulated pluripotency and a glycolytic metabolism in human hepatic and biliary tree stem/progenitor cells28. These results are important for stem cell biology, and confirm earlier results where other cell types were exposed to µg6,7. Cho et al.30 examined endometrial stroma cells exposed to 3D clinorotation and showed that µg inhibited decidualisation by reducing forkhead box O3 (FOXO3a) expression, autophagic flux and proliferation, as well as decreasing protein kinase B (Akt) activity, matrix metallopeptidase 2 (MMP2) expression and migration. They suggested that µg during spaceflight might lead to an unreceptive endometrium by suppressing decidualisation potential30.

Finally, an animal study investigated the early effects of 56Fe irradiation in mice, showing specific short-term changes in neuropathology and behaviour31, with differences in dose, sex, and disease predilection. Therefore, future studies assessing the risks of space radiation exposure seem to be important for space travel moving forward.

In conclusion, the ‘Gravitational biology and space medicine’ Collection gives a broad overview of the different space research topics (Fig. 1). It comprises in vivo and in vitro studies investigating health problems for crewmembers, but also includes basic scientific cell experiments and studies with Euglena gracilis exposed to PF maneuvers, where hierarchical clustering showed that changes were induced by the different accelerations32.

Figure 1
figure1

Compilation of studies contributed to the Collection ‘Gravitational biology and space medicine’. Parts of the figure were drawn by using pictures from Servier Medical Art (http://smart.servier.com/), licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/).

Change history

  • 19 November 2019

    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Grimm, D. Guest Edited Collection: Gravitational biology and space medicine. Sci Rep 9, 14399 (2019). https://doi.org/10.1038/s41598-019-51231-8

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