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Tissue Chips in Space: Modeling Human Diseases in Microgravity

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Abstract

Purpose

Microphysiological systems (MPS), also known as “organs-on-chips” or “tissue chips,” leverage recent advances in cell biology, tissue engineering, and microfabrication to create in vitro models of human organs and tissues. These systems offer promising solutions for modeling human physiology and disease in vitro and have multiple applications in areas where traditional cell culture and animal models fall short. Recently, the National Center for Advancing Translational Sciences (NCATS) at the National Institutes of Health (NIH) and the International Space Station (ISS) U.S. National Laboratory have coordinated efforts to facilitate the launch and use of these MPS platforms onboard the ISS. Here, we provide an introduction to the NIH Tissue Chips in Space initiative and an overview of the coordinated efforts between NIH and the ISS National Laboratory. We also highlight the current progress in addressing the scientific and technical challenges encountered in the development of these ambitious projects. Finally, we describe the potential impact of the Tissue Chips in Space program for the MPS field as well as the wider biomedical and health research communities.

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References

  1. Waring MJ, Arrowsmith J, Leach AR, Leeson PD, Mandrell S, Owen RM, et al. An analysis of the attrition of drug candidates from four major pharmaceutical companies. Nat Rev Drug Discov. 2015;14:475.

    Article  CAS  PubMed  Google Scholar 

  2. Low LA, Tagle DA. Tissue chips - innovative tools for drug development and disease modeling. Lab Chip. 2017;17(18):3026–36.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Biolo G, Heer M, Narici M, Strollo F. Microgravity as a model of ageing. Curr Opin Clin Nutr. 2003;6(1):31–40.

    Article  Google Scholar 

  4. Garrett-Bakelman FE, Darshi M, Green SJ, Gur RC, Lin L, Macias BR, et al. The NASA Twins Study: A multidimensional analysis of a year-long human spaceflight. Science. 2019;364(6436):eaau8650.

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Hughes-Fulford M, Chang TT, Martinez EM, Li C-F. Spaceflight alters expression of microRNA during T-cell activation. FASEB J. 2015;29(12):4893–900.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Xu H, Wu F, Zhang H, Yang C, Li K, Wang H, et al. Actin cytoskeleton mediates BMP2-Smad signaling via calponin 1 in preosteoblast under simulated microgravity. Biochimie. 2017;138:184–93.

    Article  CAS  PubMed  Google Scholar 

  7. Camberos V, Baio J, Bailey L, Hasaniya N, Lopez LV, Kearns-Jonker M. Effects of spaceflight and simulated microgravity on YAP1 expression in cardiovascular progenitors: implications for cell-based repair. Int J Mol Sci. 2019;20(11):2742.

    Article  CAS  PubMed Central  Google Scholar 

  8. Cazzaniga A, Locatelli L, Castiglioni S, Maier JAM. The dynamic adaptation of primary human endothelial cells to simulated microgravity. FASEB J. 2019;33(5):5957–66.

    Article  CAS  PubMed  Google Scholar 

  9. Zhang X, Li L, Bai Y, Shi R, Wei H, Zhang S. Mouse undifferentiated spermatogonial stem cells cultured as aggregates under simulated microgravity. Andrologia. 2014;46(9):1013–21.

    Article  CAS  PubMed  Google Scholar 

  10. Masiello MG, Cucina A, Proietti S, Palombo A, Coluccia P, D'Anselmi F, et al. Phenotypic switch induced by simulated microgravity on MDA-MB-231 breast cancer cells. Biomed Res Int. 2014;2014:652434–4.

    Article  Google Scholar 

  11. Crabbé A, Nielsen-Preiss SM, Woolley CM, Barrila J, Buchanan K, McCracken J, et al. Spaceflight enhances cell aggregation and random budding in Candida albicans. PLoS One. 2013;8(12):e80677–7.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Jha R, Wu Q, Singh M, Preininger MK, Han P, Ding G, C, et al. Simulated microgravity and 3D culture enhance induction, viability, proliferation and differentiation of cardiac progenitors from human pluripotent stem cells. Scientific Reports. 2016;6:30956–30956.

  13. Shi W, Xie Y, He J, Zhou J, Gao Y, Wei W, et al. Microgravity induces inhibition of osteoblastic differentiation and mineralization through abrogating primary cilia. Sci Rep. 2017;7(1):1866–6.

  14. Xue L, Li Y, Chen J. Duration of simulated microgravity affects the differentiation of mesenchymal stem cells. Mol Med Rep. 2017;15(5):3011–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Fuentes TI, Appleby N, Raya M, Bailey L, Hasaniya N, Stodieck L, et al. Simulated microgravity exerts an age-dependent effect on the differentiation of cardiovascular progenitors isolated from the human heart. PLoS One. 2015;10(7):e0132378–8.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Grigoryan EN, Radugina EA. Behavior of stem-like cells, precursors for tissue regeneration in Urodela, under conditions of microgravity. Stem Cells Dev. 2019;28(7):423–37.

    Article  CAS  PubMed  Google Scholar 

  17. Capri M, Morsiani C, Santoro A, Moriggi M, Conte M, Martucci M, et al. Recovery from 6-month spaceflight at the international Space Station: muscle-related stress into a proinflammatory setting. FASEB J. 2019;33(4):5168–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Honda Y, Honda S, Narici M, Szewczyk NJ. Spaceflight and ageing: reflecting on Caenorhabditis elegans in space. Gerontology. 2014;60(2):138–42.

    Article  PubMed  Google Scholar 

  19. Crucian BE, Choukèr A, Simpson RJ, Mehta S, Marshall G, Smith SM, et al. Immune system Dysregulation during spaceflight: potential countermeasures for deep space exploration missions. Front Immunol. 2018;9:1437–7.

  20. Sibonga J, Matsumoto T, Jones J, Shapiro J, Lang T, Shackelford L, S et al. Resistive exercise in astronauts on prolonged spaceflights provides partial protection against spaceflight-induced bone loss Bone 2019;128:112037.

    Article  CAS  PubMed  Google Scholar 

  21. Smith SM, Heer M, Shackelford LC, Sibonga JD, Spatz J, Pietrzyk RA, et al. Bone metabolism and renal stone risk during international Space Station missions. Bone. 2015;81:712–20.

    Article  CAS  PubMed  Google Scholar 

  22. Khine HW, Steding-Ehrenborg K, Hastings JL, Kowal J, Daniels JD, Page RL, et al. Effects of prolonged spaceflight on atrial size, atrial electrophysiology, and risk of atrial fibrillation. Circ Arrhythm Electrophysiol. 2018;11(5):e005959.

  23. Yeung CK, Koenig P, Countryman S, Thummel KE, Himmelfarb J, Kelly EJ. Tissue chips in space—challenges and opportunities. Clinical and Translational Science. 2019;0(0).

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ACKNOWLEDGMENTS AND DISCLOSURES

We thank NASA for their support of this initiative. We also thank astronauts Anne McClain, David St-Jacques, Christina Hammock Koch, and Nick Hague for their laboratory support during Expedition 59 and for support for flight experiments launched on CRS-SpaceX 17 in May 2019.

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Correspondence to Lucie A. Low.

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Guest Editors: Sara Eyal and Hartmut Derendorf

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Low, L.A., Giulianotti, M.A. Tissue Chips in Space: Modeling Human Diseases in Microgravity. Pharm Res 37, 8 (2020). https://doi.org/10.1007/s11095-019-2742-0

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