So Long, and Thanks for All the Antagomirs: Space Radiation Damage Rescued by Inhibition of Key Spaceflight Associated miRNAs

Author:

McDonald J. Tyson1,Farmerie Lily2ORCID,Johnson Meghan2,Park Jiwoon3ORCID,Kim JangKeun4,Overbey Eliah4,Haltom Jeffrey5,Singh Urminder6,Wurtele Eve Syrkin6,Enguita Francisco7ORCID,Zaksas Victoria8ORCID,Guarnieri Joseph9,Topper Michael10,Wallace Douglas11,Baylin Stephen12,Meller Robert13,Muratani Masafumi14ORCID,Porterfield D. Marshall15,Kaufman Brett16ORCID,Mori Marcelo17ORCID,Mason Christopher4ORCID,Grabham Peter18,Beheshti Afshin19

Affiliation:

1. Georgetown University School of Medicine

2. Vascular Medicine Institute, University of Pittsburgh

3. Weill Cornell Medical College

4. Weill Cornell Medicine

5. Iowa State University

6. Center for Metabolomics, Iowa State University

7. Instituto de Medicina Molecular João Lobo Antunes, Universidade de Lisboa

8. Clever Research Lab, L.L.C.

9. The Children's Hospital of Philadelphia

10. The Johns Hopkins Medical Institutions

11. Center for Mitochondrial and Epigenomic Medicine, The Children's Hospital of Philadelphia

12. Johns Hopkins Medical Institutions

13. Morehouse School of Medicine

14. University of Tsukuba

15. Purdue University

16. University of Pennsylvania School of Veterinary Medicine

17. Institute of Biology, University of Campinas (Unicamp)

18. Center for Radiological Research, College of Physicians and Surgeons, Columbia University

19. Broad Institute of MIT and Harvard

Abstract

Abstract From our previous work we have shown a key miRNA signature that is associated with spaceflight can be used as a biomarker and countermeasure to mitigate the damage caused by space radiation. Here, we have further expanded on this work to determine key biological factors that are being rescued by the countermeasure treatment. We performed RNA-sequencing and transcriptomic analysis on our established 3D microvessel cell cultures exposed to simulated deep space radiation (0.5 Gy of Galactic Cosmic Radiation) with and without the antagonists to three microRNAs (i.e. antagomirs). Significant reduction of inflammation and DNA DSBs activity is observed, along with key mitochondria functions being rescued after antagomir treatment. Lastly, we compared the key genes and pathways involved with the antagomirs with astronaut data from Inspiration4 and JAXA missions to demonstrate that the key genes and pathways associated with these experiments occur in humans and this countermeasure strategy can potentially be utilized in astronauts to mitigate the space radiation response.

Publisher

Research Square Platform LLC

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