Abstract
NASA’s Space Biology and Human Research Program entities have recently spearheaded communications both internally and externally to coordinate the agency’s translational research efforts. In this paper, we strongly advocate for translational research at NASA, provide recent examples of NASA sponsored early-stage translational research, and discuss options for a path forward. Our overall objective is to help in stimulating a collaborative research across multiple disciplines and entities that, working together, will more effectively and more rapidly achieve NASA’s goals for human spaceflight.
Introduction
With the International Space Station (ISS) available for research and habitation for the next decade, there is now a precious opportunity to significantly advance the contributions of space life sciences and space medicine toward enabling the Exploration Class missions (that is, human missions beyond low-Earth orbit). Such missions are currently burdened with significant anticipated crew health and safety challenges.1 Coordinated research and development are crucial for producing effective countermeasures against the deleterious influences of spaceflight on the human body. To this end, we emphatically support the development of translational research efforts at NASA that will facilitate bi-directional information flow between basic and applied life sciences and medical operations with the goal to accelerate countermeasure development.
As identified by National Academy committees and embedded in the NASA Strategic Plan, a sustainable human spaceflight program requires robust research at both basic and applied levels to make fundamental biological discoveries and to address the known and emerging risks to human health resulting from the spaceflight environment, respectively.2–5 The Life Sciences portfolio at NASA is composed of the Space Biology program (a basic science program), the Human Research Program (HRP, an applied program), and Medical Operations (Office of Chief Health and Medical Officer). Informal translational research within these programs has taken place at NASA for decades, yet there is a need for a more coordinated effort that enables dynamic translation that can take rapid advantage of new findings. In particular, the National Academy committees recommended that NASA follows key elements of the National Institutes of Health’s (NIH) model of translational science.6,7 It was specifically recommended that the coordination and maturation of projects between each level of research be enhanced to increase knowledge transfer and identification of potential solutions for astronaut health challenges.2–4 Additionally, the translation of knowledge to Earth-based medical care has recently begun with the designation of the ISS as a National Laboratory (currently through the Center for the Advancement of Science in Space).
In this paper, we provide context for the current drivers (and needs) for translational research at NASA, briefly summarize the experience at NIH, and lay out a two-phased approach for translational research. As illustrated in Fig. 1, the first phase is basic-to-applied and the second phase is applied-to-operational. We define the levels of the research continuum as follows, consistent with the Decadal Survey’s Interim Report:5 basic research aims to generate new biological knowledge using biological systems or model organisms, applied research aims to develop countermeasures for risks to astronaut health (similar to pre-clinical research), and medical operations puts countermeasures into practice for astronauts (like operations in the clinic).
Finally, going into greater depth on the basic-to-applied window of translation, we provide examples and recommendations of early-stage research where Space Biology and HRP aim to build synergy between their existing programs. NASA’s Space Biology and HRP entities have recently spearheaded communications both internally and externally to coordinate the Agency’s translational research efforts between basic and applied levels. In this paper, we strongly advocate for translational research at NASA, provide recent examples of NASA-sponsored early-stage translational research, and discuss options for a path forward. Our overall objective is to help in stimulating the collaborative research across multiple disciplines and entities that, working together, will more effectively and more rapidly achieve NASA’s goals for human spaceflight.
NASA’s involvement in translational research
Definitions
For the purposes of this paper we will focus mainly on the translation of space life sciences research knowledge to the human challenges associated with long-duration spaceflights. Our narrow translational research focus is therefore defined as the application of basic science discoveries to the development of new preventive and therapeutic approaches supporting optimized human adaptation to space missions with extended durations and distances from Earth.
NASA’s human spaceflight challenges
The biomedical concerns and risks of human Exploration Class missions, characterized by extended duration space exposures and travel far beyond Earth, are not yet fully understood.8 Prior to an exploration mission, better definition of these risks, and the development and implementation of countermeasures must be achieved to avoid physiological and behavioral changes that could degrade the health, safety and productivity of crew members during extended ISS habitation and missions beyond Low Earth Orbit (LEO). Additionally, during exploration missions, tools are needed to monitor and manage individual and crew resiliency in the face of unplanned challenges.9
The ISS presently accommodates continuous human habitation, enabling basic and applied research and testing of new ways to thrive in space. ISS offers a unique platform that is facilitating the identification of requirements for conducting future human missions that could last for years, and the challenges associated with orbiting and even occupying other planets. Exploration Class missions beyond ISS will require detailed knowledge of what adaptations can be tolerated and those which must be countered for the long-term. These missions will also require a degree of operational resiliency and autonomy never before attempted. Human space exploration is now at a crossroads, and leaving LEO will place increasing demands on space life sciences research to support such endeavors.
Key spaceflight-related environmental factors that chronically impact human health and performance during such missions are: microgravity, confinement, and exposure to space radiation.1 We chose just four examples, profiled below, to demonstrate the value of translational research in addressing four specific risks identified by NASA for astronaut health and safety: immune response, microbe-host interactions, oxidative stress and damage, and visual impairment (VI) syndrome. There are many others on NASA’s list,10 of course, including some in broad areas such as nutrition and sleep, and surely some not yet identified. For NASA, translational research has historically been11 and is increasingly viewed as essential to better define and minimize these health risks.
Translational research: pioneered by NIH
NIH has pioneered the translational research challenge since about 2003.7 Several NIH institutes have been established under the National Center for Advancing Translational Sciences6 to develop a “Translational Pipeline” linking basic research to pre-clinical and clinical investigations7,12 that will lead to eventual utilization in the provision of health care. Both the NIH and NASA research portfolios cover a broad range of spatial scale and complexity, including microbiology, cell culture, model organisms, and an array of human biomedical studies (Fig. 1). NASA can learn much from NIH’s endeavors, and the implementation of cooperative agreements between these agencies could provide effective bridges for knowledge sharing.
Recent NASA drivers toward translational research
In 2009, after consultation with NASA, Congress determined that an objective reassessment was needed of the basic and applied research capabilities and resources available to support future human space exploration. Congress mandated that the National Research Council conduct and publish a “Decadal Survey” ultimately titled Recapturing a Future for Space Exploration: Life and Physical Sciences Research for a New Era.3 The Decadal Survey reviewed the research, development, and applications relevant to basic science and human space exploration. The Space Life and Physical Sciences research communities provided major input to the Decadal Survey and helped to shape its many broad recommendations. A key recommendation was to increase the integration of efforts toward conduct of cross-disciplinary, focused translational research and development with applications to human space risks and related areas supporting human space exploration. Another main recommendation was for NASA to constitute an integrated organization within NASA to manage these efforts. In 2011, the Space Life and Physical Science Research & Applications Division was established within NASA’s Human Exploration and Operations Mission Directorate.
Key life science elements within the SLPSRA Division include the HRP and the Space Biology program (Fig. 2). HRP created and maintains a dynamic Human Research Roadmap that defines known risks, mitigation capabilities, current knowledge gaps, and concepts for future work regarding astronaut health, performance, and safety.10 In contrast, Space Biology focuses on defining the changes in basic biological mechanisms as a result of spaceflight and has developed a set of Guiding Questions that define its research program.13 Despite the programmatic differences, there are overlapping research areas within these two programs at the basic-to-applied phase of translation, which are itemized in Fig. 2 and described below in the Examples section.
The Decadal Survey panels made recommendations for research priorities throughout the lifespan of the ISS. In Chapter 6 of the Decadal Survey, the Animal and Human Biology panel (3) made 16 key recommendations spanning multiple systems in the body of vertebrates for conduct of basic and applied research (Table 1). The panel indicated that many of these should be studied using a translational framework. Further, the panel unanimously stated that animal research be firmly integrated in the space life sciences portfolio—both within space-based and ground-based programs—to drive the translation of knowledge. Additionally, in Chapter 7 of the Decadal Survey, the Integrative and Translational Research for the Human Systems panel (3) made 11 recommendations related to crosscutting issues (CC) for humans in the space environment (Table 2). One goal of this paper is to bring stakeholders—U.S. taxpayers, Congress, the National Academies, and relevant science communities—up to date regarding NASA’s progress in building collaborative research communities in the translational area to pursue these important recommendations.
Table 1.
Identifier | Recommendation |
---|---|
AH1 | The efficacy of bisphosphonates should be tested in an adequate population of astronauts on the ISS during a 6-month mission. |
AH2 | The preservation/reversibility of bone structure/strength should be evaluated when assessing countermeasures. |
AH3 | Bone loss studies of genetically altered mice exposed to weightlessness are strongly recommended. |
AH4 | New osteoporosis drugs under clinical development should be tested in animal models of weightlessness. |
AH5 | Conduct studies to identify underlying mechanisms regulating net skeletal muscle protein balance and protein turnover during states of unloading and recovery. |
AH6 | Conduct studies to develop and test new prototype exercise devices and to optimize physical activity paradigms/prescriptions targeting multisystem countermeasures. |
AH7 | Determine the daily levels and pattern of recruitment of flexor and extensor muscles of the neck, trunk, arms, and legs at 1 g and after being in a novel gravitational environment for up to 6 months. |
AH8 | Determine the basic mechanisms, adaptations, and clinical significance of changes in regional vascular/interstitial pressures (starling forces) during long-duration space missions. |
AH9 | Investigate the effects of prolonged periods of microgravity and partial gravity (3/8 or 1/6 g) on the determinants of task-specific, enabling levels of work capacity. |
AH10 | Determine the integrative mechanisms of orthostatic intolerance after restoration of gravitational gradients (both 1 and 3/8 g). |
AH11 | Collaborative studies among flight medicine and cardiovascular epidemiologists are recommended to determine the best screening strategies to avoid flying astronauts with subclinical coronary heart disease that could become manifest during a long-duration exploration-class mission (3 years). |
AH12 | Determine the amount and site of the deposition of aerosols of different sizes in the lungs of humans and animals in microgravity. |
AH13 | Multiple parameters of T cell activation in cells should be obtained from astronauts before and after re-entry to establish which parameters are altered during flight. |
AH14 | Both to address the mechanism(s) of the changes in the immune system and to develop measures to limit the changes, data from multiple organ/system-based studies need to be integrated. |
AH15 | Perform mouse studies of immunization and challenge on the ISS, using immune samples acquired both prior to and immediately upon re-entry, to establish the biological relevance of the changes observed in the immune system. Parameters examined need to be aligned with those in humans influenced by flight. |
AH16 | Studies should be conducted on transmission across generations of structural and functional changes induced by exposure to space during development. Ground-based studies should be conducted to develop specialized habitats to support reproducing and developing rodents in space. |
Reprinted with permission from Recapturing a Future for Space Exploration: Life and Physical Sciences Research for a New Era (2011) by the National Academy of Sciences, Courtesy of the National Academies Press, Washington D.C.
Table 2.
Identifier | Recommendation |
---|---|
CC1 | To ensure the safety of future commercial orbital and exploration crews, quantify post-landing vertigo and orthostatic intolerance in a sufficiently large sample of returning ISS crews, as part of the immediate post-flight medical exam. |
CC2 | Determine whether AG is needed as a multisystem countermeasure and whether continuous large radius AG is needed or intermittent exercise within lower-body negative pressure or short-radius AG is sufficient. Human studies in ground laboratories are essential to establish dose-response relationships, and what gravity level, gradient, rotations per minute, duration, and frequency are adequate. |
CC3 | Conduct studies on humans to determine whether there is an effect of gravity on micronucleation and/or intrapulmonary shunting or whether the unexpectedly low prevalence of decompression sickness on the space shuttle/ISS is due to underreporting. Conduct studies to determine operationally acceptable low suit pressure and hypobaric hypoxia limits. |
CC4 | Determine optimal dietary strategies for crews and food preservation strategies that will maintain bioavailability for 12 or more months. |
CC5 | Initiate a robust food science program focused on preserving nutrient stability for 3 or more years. |
CC6 | Include food and energy intake as an outcome variable in dietary intervention trials in humans. |
CC7 | Conduct longitudinal studies of astronauts for cataract incidence, quality, and pathology related to radiation exposures to understand both cataract risk and radiation-induced late tissue toxicities in humans. |
CC8 | Expand the use of animal studies to assess space radiation risks to humans from cancer, cataracts, cardiovascular disease, neurologic dysfunction, degenerative diseases, and acute toxicities such as fever, nausea, bone marrow suppression, and others. |
CC9 | Continue ground-based cellular studies to develop end points and markers for acute and late radiation toxicities, using radiation facilities that are able to mimic space radiation exposures. |
CC10 | Expand understanding of gender differences in adaptation to the spaceflight environment through flight- and ground-based research, particularly potential differences in bone, muscle, and cardiovascular function and longterm radiation risks. |
CC11 | Investigate the biophysical principles of thermal balance to determine whether microgravity reduces the threshold for thermal intolerance. |
Reprinted with permission from Recapturing a Future for Space Exploration: Life and Physical Sciences Research for a New Era (2011) by the National Academy of Sciences, Courtesy of the National Academies Press, Washington DC
NASA’s current translational research approach
Several recent NASA-sponsored activities demonstrate an increased Agency commitment to two phases of translation (Fig. 1). Within the basic-to-applied phase, a collaborative workshop was held by NASA JSC and ARC in 2004 that addressed “Animal Research in Support of Human Space Exploration” before the translational research terminology was commonly used.14 Further, several recent events have been held to systematically advance NASA’s translational research discussions within the basic and applied space life sciences communities, including: an Artificial Gravity Workshop (responsive to the recommendations AH9-10 in Table 1 and CC2 in Table 2);15 symposia at the American Society for Gravitational Space Research (ASGSR) annual meetings in 201416and 2015;17 and the annual HRP Investigators Workshops in 2015 and 2016. Finally, an internal analysis of the Space Biology and HRP research plans has pointed to areas, described in the examples section below and in Fig. 2, that are ripe for synergism.
Within the applied-to-operational phase, HRP established a Translational Research Institute, in October 2016, with a key goal to recruit funded, terrestrial biomedical research entities in furthering NASA translational research goals,18–20 and to help mature countermeasures and technologies for use in medical operations. Taken together, these efforts demonstrate new activities to facilitate translation from basic science to operations.
But how can translational research most effectively be pursued using existing resources? Team science is one solution21 and has been used successfully by NASA in the past. Additionally, enhanced institutional coordination within NASA and between federal funding agencies, as well as relevant non-governmental organizations, is needed to spur translation. A systematic approach to identify collaborative translational opportunities, for example by text analytics,22 would have benefits for investigators as well as NASA program managers. Text analytics is one method to systematically and automatically examine published papers for linkages based on common concepts (manifest in authorship, keywords, references, methods). This approach would allow the visualization of domains where research has been explored jointly within animals and humans or where the gaps in knowledge reside.
The Decadal Survey (3) provides guidance on how to structure a fully-integrated translational program by partitioning the life sciences research portfolio into two dimensions. Horizontal integration of projects is the first dimension and requires multidisciplinary approaches to solve complex problems, often within a given organism type. The second dimension, vertical translation, requires meaningful interactions among basic, applied, and operational scientists to translate fundamental discoveries to human treatments, such as using cell biology and model organism research to address human problems, for example in immune system response challenges.
The NIH experience has shown that the horizontal integration of research knowledge is essential for developing a comprehensive understanding of physiology and to effectively solve health problems.23 NASA has a successful record in this domain that should continue, for example, with its BioSpecimen Sharing Programs. Researchers have recently shared tissues from specific animals on a late Shuttle mission (STS-131),24–31 and the most recent Russian Bion biosatellite mission;32–35 sharing was in the form of preserved tissues from NASA’s Life Sciences Data Archive.36 Further, new Omic-science studies like NASA’s emerging GeneLab open-science data and biosample repository37 and the recent astronaut Twins Study38 enable big-data collection, analytics, and horizontal integration. Finally, restoring the gravity vector artificially via chronic whole-body centrifugation may solve issues in multiple tissues, simultaneously.
In contrast, vertical translation requires that investigators along the research continuum from basic to operational (Fig. 1) interact regularly to share ideas. Examples of vertical translation at NASA are in the recent International Life Sciences Research Announcement awards (NASA, European, Japanese, and Canadian space program research solicitations),39 GeneLab,37 and the recent call for proposals in the area of artificial gravity (AG).40 All of these planned research projects span multiple levels of the translational pipeline. Additionally, vertically-integrated team science occurs through NASA Specialized Centers of Research (NSCOR)41–44 and the National Space Biomedical Research Institute’s centers for radiation research,45–47 which aim to identify and translate countermeasure candidates for radiation-induced insults (Table 2: CC7–CC9). There is surely untapped value to be derived from additional vertical translation within NASA programs. Some existing overlap and synergism between HRP and Space Biology goals and approaches amenable to both horizontal and vertical translation are shown in Fig. 2.
Informally, vertical translation has occurred at NASA for many years11 with a conceptual maturation path shown in Fig. 1. For example, molecular mechanisms underlying the bone loss resulting from musculoskeletal disuse have been demonstrated in ground-based models,48–50 responding to recommendations AH2-4 (Table 1). Further, two precursors to osteoporosis drugs have been tested in space-flown or ground-based mice and shown to be effective at preventing weightlessness-induced bone loss,49–51 responsive to recommendations AH2, AH4 (Table 1). Thus, these drugs give HRP and Medical Operations additional potential countermeasures besides exercise52 and Alendronate53 to combat bone loss during spaceflight. Additional specific examples of vertical translation are described in the examples below.
Examples of NASA life sciences basic-to-applied translational research
Progress in four specific areas is profiled below, each of which is a NASA “Health and Human Performance Risk for Space Exploration”.8 All demonstrate linkages between basic and applied research and involve on-going collaborations between Space Biology and the HRP. These examples illustrate ongoing opportunities for synergy between basic and applied researchers and these NASA programs to enhance and accelerate health-risk reduction.
Immune response
The immune system is constantly adapting and is particularly responsive to unique environments such as those in spaceflight, especially for exposures of the long durations required by exploration missions beyond LEO. Immune system dysregulation (decreased responsiveness) has been seen during and after spaceflight and ground-space analog tests by studying humans,54 animals,55 and relevant cell cultures56 and are a priority area for study (AH13-15, Table 1). The specific causes are not yet clear, but are likely linked to one or more of the following factors: physiological stress, circadian rhythm disruption, microgravity exposure, isolation, altered nutrition, or radiation exposure.57 Further, the spaceflight environment compounds crew health risks as some microorganisms become more virulent (see below) and resistant to antibiotic drugs.
Even though the reactivation of latent viruses has been well documented in crewmembers,58 it is still unclear if the compromised immune response can lead to increased susceptibility to disease. There is not a sufficiently accurate ground-based analog to study immune suppression from spaceflight. However, extreme occupational environments such as Antarctica winter-over and the Aquarius undersea station enable aspects of immune dysregulation to be studied under similar stressors. Additionally, many valuable analog studies with animals and cells have been conducted, including unloading of rodents,59 and cell cultures and bioreactors.56,60 These studies have investigated immune response mechanisms and can allow the use of controlled diets, increased radiation levels and other factors that are not possible in human research.
Microbe-host interactions
Preventive measures limit the presence of many medically significant microorganisms during spaceflight missions, but microbial infection of crewmembers cannot be completely prevented. Spaceflight experiments have demonstrated unique and heterogeneous microbial responses in spaceflight ecosystems and cultures,61,62 although the mechanisms behind those responses and their operational relevance remain unclear. In 2007, the operational importance of these microbial responses increased, as the results of Space Biology experiments aboard STS-115 and STS-123 demonstrated that an enteric pathogen (Salmonella typhimurium) increased in virulence in a mouse model of infection,63,64 responding to recommendation AH15 (Table 1). These studies can improve our understanding of the potential consequences to astronauts of elevated microbial virulence during long-duration missions.
Evidence for increased microbial virulence has recently been collected and reported from both spaceflight-analog systems and actual spaceflight.61,65,66 Although the conduct of virulence studies during spaceflight is challenging and often impractical in humans, data are being collected as part of the ISS Microbial Observatory,62 recent astronaut and rodent microbiome studies,67–69 and the edible plant studies (e.g., Veggie).70,71 When available, these results can improve our understanding of the astronaut-microbe interaction and of the potential health risks to the astronaut.
Oxidative stress
The novel environmental conditions of spaceflight, and their combination, may affect both the generation and safe processing of reactive oxygen or nitrogen species.72,73 Evidence for oxidative-related issues in astronauts (or their analogs) can be found in the HRP Evidence Reports covering inadequate nutrition,74 extravehicular activity,75 and exposure to ionizing radiation.47,76–79 NASA has successfully used horizontally-integrated team science to understand and mitigate components of radiation-induced oxidative stress42–44 in mice.
Visual impairment/intracranial pressure (VI/IP)
During and after long-duration spaceflights, some astronauts have reported noticeable, persistent VIs accompanied by ophthalmic changes including globe flattening, choroidal folds, optic-disc edema, and optic-nerve kinking.80 To date, clinically significant changes have been observed in male, but not female, astronauts,81 identifying a not yet understood sex difference, CC10 (Table 2). Increased intracranial pressure and optic-disc swelling (papilledema) may underlie these potentially irreversible changes.81 Current research is analyzing the effects of lowering cranial hypertension by using lower body negative pressure in astronauts during flight and bedrest,82 supporting the CC2 goal (Table 2).
Clinical signs and symptoms observed in astronauts have informed and focused important mechanistic studies exemplifying reciprocal translation at NASA (i.e., applied to basic). For example, retinas of female mice flown on the shuttle (STS-133, STS-135), acquired by the BioSpecimen Sharing Program, exhibit altered gene expression and increased oxidative stress,83 possibly causing retinal damage, degeneration, or remodeling.84,85 Other basic research is examining morphological, histological, and molecular changes in the brains and eyes of rats exposed to head-down tilt.86
Altogether, these examples are in the early stages of mechanistic understanding and countermeasure development. Already each has benefited from translational approaches. We suggest that a more coordinated programmatic effort of horizontal and vertical integration will accelerate countermeasure development. In the closing section, we provide suggestions of how enhanced translational research could materialize at NASA.
Options for NASA’s future translational research path
Given the need for acute astronaut countermeasures to enable longer-duration missions, we recommend the following steps to catalyze translational research within NASA’s Life Sciences portfolio.
Building and managing partnerships
Greater coordinated efforts in translational research are needed to understand and manage the integrated organismal response to spaceflight and enable human exploration. Current activities within NASA’s SLPSRA Division are creating new opportunities for translational science both within and external to the Agency. Tools like text analytics should aid in managing the life sciences portfolio and identify new gaps in knowledge. Other government agencies, such as NIH, and other organizations, both commercial and non-profit, have been working for a number of years on Earth-based translational research goals. NASA should partner, both nationally and internationally, with external organizations to benefit from their tools, techniques, and experience, and add NASA-unique data and translational research efforts to the much larger, continually growing, and worldwide community of translational research science.
New collaborations
NASA’s Human Research and Space Biology programs should increasingly encourage translational research proposals for upcoming NASA research announcements (NRAs),87 including proposals that span traditional program boundaries or team science proposals (horizontally or vertically-integrated teams of investigators like the NSCORs or resembling the P01 Program Project Grants offered by NIH). Additionally, phased awards allowing progression from hypothesis-driven science to countermeasure development would enable vertical translation across NASA’s life sciences portfolio (Figs. 1, 2). Finally, proposals with international collaborations are encouraged to leverage the ISS platform and unique national resources (see the open NRAs and the International Space Life Sciences Working Group for research announcements).
NASA’s open science and data sharing
Open Science approaches, allowing transparency and data sharing at all levels of society, are being developed at NASA to provide greater access to data and tissue sharing from both space and ground-based research. The goal is to engage researchers both within and outside of the NASA community (e.g., academia, NIH, Department of Defense, etc). These steps are essential for both optimizing the use of these valuable resources and facilitating translational research goals. NASA should continue the development and expansion of Open Science systems, such as GeneLab, to enable translational research for the broadest research community.
Education, communications, and advocacy
Increased activity in the Education, Communication, and Advocacy areas will be fundamental to achieve translational research goals and is a mandate of the HRP Translational Research Institute. Additionally, organizations such as the ASGSR are discussing options to engage their members who span biology, human research, physical sciences, life support, related technology development, and commercial applications in translational research pursuits. NASA should develop research fellowships, as well as educational and scientific communication materials specifically tailored to the Agency’s translational research goals and partner with external organizations, wherever possible, to leverage the advocacy those organizations can provide.
Closing
In summary, translation research is a two-phased effort at NASA and will help accelerate countermeasure development for exploration missions. We have specified four areas where synergy within the existing program structures seems promising and have suggested ways in which program coordination and team science approaches can facilitate translation from discovery to development to implementation.
Acknowledgements
Many of the ideas and concepts reflected in this perspective were prepared by and presented at recent NASA Workshops by our colleagues: William Paloski (Director, NASA JSC HRP), David Tomko (NASA HQ, Program Executive, Space Biology Program), and Barbara Corbin (NASA JSC, Deputy Manager, HRP). We wish to thank them for guiding the groundwork and facilitating continuing work on this effort. Additionally, we thank David Tomko for providing expert consultation and the initial draft of Fig. 1. We thank Sidney Sun, Chris Maese, Ruth Globus, Ken Souza, and Marianne Sowa at NASA ARC and John Charles, David Baumann, and Craig Kundrot at NASA JSC for expert consultation.The Human Health Countermeasures element of the HRP at NASA provided funding for this paper.
Author Contributions
Each author significantly contributed to the writing and editing of the manuscript.
Competing Interests
The authors declare that they have no conflict of interest.
References
- 1.NASA. Journey to Mars: Pioneering Next Steps in Space Exploration. NASA, NP-2015-08-2018-HQ. https://www.nasa.gov/sites/default/files/atoms/files/journey-to-mars-next-steps-20151008_508.pdf (2015).
- 2.National Academy Of Sciences. A Strategy for Research in Space Biology and Medicine in the New Century. in Committee on Space Biology and Medicine Space Studies Board (ed.) (National Academies Press, 1998).
- 3.National Academy Of Sciences. Recapturing a Future for Space Exploration: Life and Physical Sciences Research for a New Era. in Committee for the Decadal Survey on Biological and Physical Sciences in Space (ed.) (National Academies Press, 2011).
- 4.NASA. NASA strategic plan. NASA, NP-2014-01-964-HQ (2014).
- 5.NationalAcademyOfSciences. Life and Physical Sciences Research for a New Era of Space Exploration: An Interim Report. in Committee for the Decadal Survey on Biological and Physical Sciences in Space (ed.) (National Academies Press, 2010).
- 6.National Institutes Of Health. National Center for Advancing Translational Scienceshttp://ncats.nih.gov/research (2016).
- 7.Zerhouni E. Medicine. The NIH Roadmap. Science. 2003;302(5642):63–72. doi: 10.1126/science.1091867. [DOI] [PubMed] [Google Scholar]
- 8.McPhee J. C., Charles J. B. Human health and peformance risks of space exploration missions. NASA SP-2009-3405 (2009).
- 9.Shelhamer M. A call for research to assess and promote functional resilience in astronaut crews. J. Appl. Physiol. 2016;120(4):471–472. doi: 10.1152/japplphysiol.00717.2015. [DOI] [PubMed] [Google Scholar]
- 10.NASA. Human research program: human research roadmaphttp://humanresearchroadmap.nasa.gov (2016).
- 11.NASA. Translational cell & animal research, 1965-2011https://www.nasa.gov/ames/research/space-biosciences/nasa-special-publication-on-translational-cell-and-animal-research (2015).
- 12.Alberts B, Kirschner MW, Tilghman S, Varmus H. Rescuing US biomedical research from its systemic flaws. Proc. Natl. Acad. Sci. USA. 2014;111(16):5773–5777. doi: 10.1073/pnas.1404402111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Tomko D. L., et al.NASA space biology science plan 2016-2025https://www.nasa.gov/sites/default/files/atoms/files/16-03-23_sb_plan.pdf (2016).
- 14.Jennings D., Souza K. Meeting Report: Animal Research in Support of Human Space Exploration (Workshop at National Academy of Sciences, 2004).
- 15.Paloski W. H., Charles J. B. International workshop on research and operational considerations for artificial gravity countermeasures. NASA, 2014 TM-2014-217394 (2014).
- 16.American Society for Gravitational and Space Research. Translational research roadmap workshophttps://ac.arc.nasa.gov/p1lf9sla9od (2014).
- 17.American Society for Gravitational and Space Research. Translationally focused symposia (Symposia V)https://www.asgsr.org/index.php/2015-annual-meeting-video-streams (2015).
- 18.NASA. HRP translational research institute (HTRI) draft cooperative agreement notice (CAN)http://procurement.jsc.nasa.gov/htri/.
- 19.Sheetz MP. Can small institutes address some problems facing biomedical researchers? Mol. Biol. Cell. 2014;25(21):3267–3269. doi: 10.1091/mbc.E14-05-1017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.NASA Establishes institute to explore new ways to protect astronauts [press release]. July 20(2016).
- 21.National Research Council. Enhancing the Effectiveness of Team Science (The National Academies Press, 2015). [PubMed]
- 22.Dunne C, Shneiderman B, Gove R, Klavans J, Dorr B. Rapid understanding of scientific paper collections: Integrating statistics, text analytics, and visualization. J. Am. Soc. Inf. Sci. Technol. 2012;63(12):2351–2369. doi: 10.1002/asi.22652. [DOI] [Google Scholar]
- 23.Joyner MJ. Giant sucking sound: can physiology fill the intellectual void left by the reductionists? J. Appl. Physiol. 2011;111(2):335–342. doi: 10.1152/japplphysiol.00565.2011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Chang TT, Spurlock SM, Candelario TL, Grenon SM, Hughes-Fulford M. Spaceflight impairs antigen-specific tolerance induction in vivo and increases inflammatory cytokines. FASEB J. 2015;29(10):4122–4132. doi: 10.1096/fj.15-275073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Bailey JF, Hargens AR, Cheng KK, Lotz JC. Effect of microgravity on the biomechanical properties of lumbar and caudal intervertebral discs in mice. J. Biomech. 2014;47(12):2983–2988. doi: 10.1016/j.jbiomech.2014.07.005. [DOI] [PubMed] [Google Scholar]
- 26.Blaber EA, et al. Mechanical unloading of bone in microgravity reduces mesenchymal and hematopoietic stem cell-mediated tissue regeneration. Stem. Cell. Res. 2014;13(2):181–201. doi: 10.1016/j.scr.2014.05.005. [DOI] [PubMed] [Google Scholar]
- 27.Zhang B, Cory E, Bhattacharya R, Sah R, Hargens AR. Fifteen days of microgravity causes growth in calvaria of mice. Bone. 2013;56(2):290–295. doi: 10.1016/j.bone.2013.06.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Blaber EA, et al. Microgravity induces pelvic bone loss through osteoclastic activity, osteocytic osteolysis, and osteoblastic cell cycle inhibition by CDKN1a/p21. PLoS One. 2013;8(4):e61372. doi: 10.1371/journal.pone.0061372. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Behnke BJ, et al. Effects of spaceflight and ground recovery on mesenteric artery and vein constrictor properties in mice. FASEB J. 2013;27(1):399–409. doi: 10.1096/fj.12-218503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Mednieks M, Khatri A, Rubenstein R, Burleson JA, Hand AR. Microgravity alters the expression of salivary proteins. Oral. Health. Dent. Manag. 2014;13(2):211–216. [PubMed] [Google Scholar]
- 31.Stabley JN, et al. Spaceflight reduces vasoconstrictor responsiveness of skeletal muscle resistance arteries in mice. J. Appl. Physiol. 2012;113(9):1439–1445. doi: 10.1152/japplphysiol.00772.2012. [DOI] [PubMed] [Google Scholar]
- 32.Berg-Johansen B., Liebenberg E. C., Li A., Macias B. R., Hargens A. R., Lotz J. C. Spaceflight-induced bone loss alters failure mode and reduces bending strength in murine spinal segments. J. Orthop. Res.34(1), 48–57 (2016). [DOI] [PMC free article] [PubMed]
- 33.Ulanova A, et al. Isoform composition and gene expression of thick and thin filament proteins in striated muscles of mice after 30-day space flight. Biomed. Res. Int. 2015;2015:104735. doi: 10.1155/2015/104735. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Sofronova SI, et al. Spaceflight on the Bion-M1 biosatellite alters cerebral artery vasomotor and mechanical properties in mice. J. Appl. Physiol. 2015;118(7):830–838. doi: 10.1152/japplphysiol.00976.2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Andreev-Andrievskiy A, et al. Mice in Bion-M 1 space mission: training and selection. PLoS ONE. 2014;9(8):e104830. doi: 10.1371/journal.pone.0104830. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.NASA. Life sciences data archive (LSDA)https://lsda.jsc.nasa.gov/lsda_home.aspx (2016).
- 37.NASA. GeneLabhttp://genelab.nasa.gov/ (2016).
- 38.NASA. Twins studyhttps://www.nasa.gov/twins-study (2016).
- 39.NASA. New research headed to station helping NASA explore the universe (updated February 10) https://www.nasa.gov/content/new-research-headed-to-station-helping-nasa-explore-the-universe/ (2015).
- 40.NASA. Human research program, human exploration research opportunities (HERO), NNJ15ZSA001N-AG, Appendix D, Artificial Gravity Opportunity http://nspires.nasaprs.com/external/solicitations/solicitations.do?id=NNJ15ZSA001N&method=programElementsAll&path=open (2015).
- 41.NASA. Space radiation program element: NASA specialized centers of research (NSCOR)https://spaceradiation.jsc.nasa.gov/research/ (2015).
- 42.Olsen RH, Johnson LA, Zuloaga DG, Limoli CL, Raber J. Enhanced hippocampus-dependent memory and reduced anxiety in mice over-expressing human catalase in mitochondria. J. Neurochem. 2013;125(2):303–313. doi: 10.1111/jnc.12187. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Liao AC, et al. Mitochondrial-targeted human catalase affords neuroprotection from proton irradiation. Radiat. Res. 2013;180(1):1–6. doi: 10.1667/RR3339.1. [DOI] [PubMed] [Google Scholar]
- 44.Parihar VK, et al. Targeted overexpression of mitochondrial catalase prevents radiation-induced cognitive dysfunction. Antioxid. Redox. Signal. 2015;22(1):78–91. doi: 10.1089/ars.2014.5929. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Boerma M. Center for research on cardiac, vascular, and acute effects of space radiationhttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10329 (2014).
- 46.Kennedy A. R. Center of acute radiation researchhttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10056 (2008).
- 47.Chancellor JC, Scott GB, Sutton JP. Space radiation: the number one risk to astronaut health beyond low earth orbit. Life (Basel) 2014;4(3):491–510. doi: 10.3390/life4030491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Xiong J, et al. Matrix-embedded cells control osteoclast formation. Nat. Med. 2011;17(10):1235–1241. doi: 10.1038/nm.2448. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Spatz JM, et al. Sclerostin antibody inhibits skeletal deterioration due to reduced mechanical loading. J. Bone Miner. Res. 2013;28(4):865–874. doi: 10.1002/jbmr.1807. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Spatz JM, et al. Serum sclerostin increases in healthy adult men during bed rest. J. Clin. Endocrinol. Metab. 2012;97(9):E1736–E1740. doi: 10.1210/jc.2012-1579. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Lloyd SA, et al. Osteoprotegerin is an effective countermeasure for spaceflight-induced bone loss in mice. Bone. 2015;81:562–572. doi: 10.1016/j.bone.2015.08.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Smith SM, et al. Benefits for bone from resistance exercise and nutrition in long-duration spaceflight: Evidence from biochemistry and densitometry. J. Bone Miner. Res. 2012;27(9):1896–1906. doi: 10.1002/jbmr.1647. [DOI] [PubMed] [Google Scholar]
- 53.Leblanc A, et al. Bisphosphonates as a supplement to exercise to protect bone during long-duration spaceflight. Osteoporos. Int. 2013;24(7):2105–2114. doi: 10.1007/s00198-012-2243-z. [DOI] [PubMed] [Google Scholar]
- 54.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(10):778–786. doi: 10.1089/jir.2013.0129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Marcu O, et al. Innate immune responses of Drosophila melanogaster are altered by spaceflight. PLoS One. 2011;6(1):e15361. doi: 10.1371/journal.pone.0015361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Boonyaratanakornkit JB, et al. Key gravity-sensitive signaling pathways drive T cell activation. FASEB J. 2005;19(14):2020–2022. doi: 10.1096/fj.05-3778fje. [DOI] [PubMed] [Google Scholar]
- 57.Crucian B., Kunz H., Sams C. F. Risk of crew adverse health event due to altered immune responsehttp://humanresearchroadmap.nasa.gov/Evidence/reports/Immune_2015-05.pdf (2015).
- 58.Mehta SK, et al. Multiple latent viruses reactivate in astronauts during Space Shuttle missions. Brain Behav. Immun. 2014;41:210–217. doi: 10.1016/j.bbi.2014.05.014. [DOI] [PubMed] [Google Scholar]
- 59.Zhou Y, et al. Effect of solar particle event radiation and hindlimb suspension on gastrointestinal tract bacterial translocation and immune activation. PLoS One. 2012;7(9):e44329. doi: 10.1371/journal.pone.0044329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Fitzgerald W, et al. Immune suppression of human lymphoid tissues and cells in rotating suspension culture and onboard the International Space Station. In Vitro Cell. Dev. Biol. Anim. 2009;45(10):622–632. doi: 10.1007/s11626-009-9225-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Chatterjee A., Bhattacharya S., Ott C. M. Risk of adverse health effects due to alterations in host-microorganism interactions. Available from: http://humanresearchroadmap.nasa.gov/Evidence/reports/Microhost.pdf (2012).
- 62.Castro S., Smith D. J., Ott C. M. A researcher’s guide to the ISS: Microbial research. NASA, NP-2013-06-012-JSC (2013).
- 63.Wilson JW, et al. Space flight alters bacterial gene expression and virulence and reveals a role for global regulator Hfq. Proc. Natl. Acad. Sci. USA. 2007;104(41):16299–16304. doi: 10.1073/pnas.0707155104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Wilson JW, et al. Media ion composition controls regulatory and virulence response of Salmonella in spaceflight. PLoS One. 2008;3(12):e3923. doi: 10.1371/journal.pone.0003923. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Nickerson CA, Ott CM, Wilson JW, Ramamurthy R, Pierson DL. Microbial responses to microgravity and other low-shear environments. Microbiol. Mol. Biol. Rev. 2004;68(2):345–361. doi: 10.1128/MMBR.68.2.345-361.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Taylor PW. Impact of space flight on bacterial virulence and antibiotic susceptibility. Infect. Drug Resist. 2015;8:249–262. doi: 10.2147/IDR.S67275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Lorenzi H. Study of the impact of long-term space travel on the astronaut’s microbiomehttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10356 (2012).
- 68.Turek F. W. HERO twin astronaut study consortium (TASC) project: Metagenomic sequencing of the bacteriome in GI tract of twin astronauts. NASA Task Bookhttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10262 (2015).
- 69.Turek F. W. Effects of spaceflight on gastrointestinal microbiota in mice: Mechanisms and Impact on multi-system physiology. NASA Task Bookhttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10262 (2015).
- 70.Massa G. Pick-and-eat salad-crop productivity, nutritional value, and acceptability to supplement the iss food systemhttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10455 (2014).
- 71.Wheeler R. Pick and eat salad crop testinghttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10461 (2014).
- 72.Finkel T, Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature. 2000;408(6809):239–247. doi: 10.1038/35041687. [DOI] [PubMed] [Google Scholar]
- 73.Nathan C, Ding A. SnapShot: Reactive Oxygen Intermediates (ROI) Cell. 2010;140(6):951–e2. doi: 10.1016/j.cell.2010.03.008. [DOI] [PubMed] [Google Scholar]
- 74.Smith S. M., Zwart S. R., Heer M. Risk of inadequate nutritionhttp://humanresearchroadmap.nasa.gov/Evidence/reports/Nutrition-20150105.pdf (2015).
- 75.Chappell S. P., Norcross J. R., Abercromby A. F. J., Gernhardt M. L. Risk of injury and compromised performance due to EVA operationshttp://humanresearchroadmap.nasa.gov/Evidence/reports/EVA.pdf (2015).
- 76.Nelson G. A., Simonsen L., Huff J. L. Risk of acute (in-flight) and late central nervous system effects from radiation exposurehttps://humanresearchroadmap.nasa.gov/Evidence/reports/CNS.pdf (2016).
- 77.Carnell L., Blattnig S., Hu S., Huff J. L., Kim M-H., Norman R., et al. Risk of acute radiation syndromes due to solar particle eventshttps://humanresearchroadmap.nasa.gov/Evidence/reports/Acute.pdf (2016).
- 78.Patel Z., Huff J. L., Saha J., Wang M., Blattnig S., Wu H. Risk Of cardiovascular disease and other degenerative tissue effects from radiation exposurehttps://humanresearchroadmap.nasa.gov/Evidence/reports/Degen.pdf (2016).
- 79.Huff J. L., Carnell L., Blattnig S., Chappell L., George K., Lumpkins S., et al. Risk of radiation carcinogenesishttps://humanresearchroadmap.nasa.gov/Evidence/reports/Cancer.pdf (2016).
- 80.Mader TH, et al. Optic disc edema, globe flattening, choroidal folds, and hyperopic shifts observed in astronauts after long-duration space flight. Ophthalmology. 2011;118(10):2058–2069. doi: 10.1016/j.ophtha.2011.06.021. [DOI] [PubMed] [Google Scholar]
- 81.Platts SH, et al. Effects of sex and gender on adaptation to space: cardiovascular alterations. J. Womens Health (Larchmt) 2014;23(11):950–955. doi: 10.1089/jwh.2014.4912. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Hargens A. R. Fluid distribution before, during and after prolonged space flight—NNX13AJ12G NASA task bookhttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10089 (2013).
- 83.Mao XW, et al. Spaceflight environment induces mitochondrial oxidative damage in ocular tissue. Radiat. Res. 2013;180(4):340–350. doi: 10.1667/RR3309.1. [DOI] [PubMed] [Google Scholar]
- 84.Zanello SB, Theriot CA, Prospero Ponce CM, Chevez-Barrios P. Spaceflight Effects and Molecular Responses in the Mouse Eye: Preliminary Observations After Shuttle Mission STS-133. Gravit. Space Res. 2013;1(1):30–46. [Google Scholar]
- 85.Theriot CA, Zanello SB. Molecular Effects of Spaceflight in the Mouse Eye after Space Shuttle Mission STS-135. Gravit. Space Res. 2014;2(1):3–24. [Google Scholar]
- 86.Fuller C. A. Head-down tilt as a model for intracranial and intraocular pressures, and retinal changes during spaceflight NASA task bookhttps://taskbook.nasaprs.com/Publication/index.cfm?action=public_query_taskbook_content&TASKID=10013 (2013).
- 87.NASA. NSPIRES: NASA solicitation and proposal integrated review and evaluation systemhttp://nspires.nasaprs.com (2016).