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Circulating Mirna Spaceflight Signature Reveals Targets to Mitigate Associated Health Risks

Authors :
Sherina Malkani
Christopher R. Chin
Egle Cekanaviciute
Marie Mortreux
Hazeem Okinula
Marcel Tarbier
Ann-sofie Schreurs
Yasaman Shirazi-fard
Candice Tahimic
Deyra N. Rodriguez
Brittany S. Sexton
Daniel Butler
Akanksha Verma
Daniela Bezdan
Ceyda Durmaz
Matthew MacKay
Ari Melnick
Cem Meydan
Sheng Li
Francine Garrett-Bakelman
Bastian Fromm
Brad W. Langhorst
Eileen T. Dimalanta
Margareth Cheng-Campbell
Elizabeth Blaber
Charles Vanderburg
Marc R. Friedländer
J. Tyson McDonald
Sylvain V Costes
Seward Rutkove
Peter Grabham
Christopher E. Mason
Afshin Beheshti
Publication Year :
2020
Publisher :
United States: NASA Center for Aerospace Information (CASI), 2020.

Abstract

We have identified and validated a spaceflight-associated microRNA (miRNA) signature that is shared by rodents and humans in response to simulated, short-duration, and long-duration spaceflight and regulates vascular damage caused by simulated deep space radiation. In previous studies, we had identified miRNAs that are predicted to regulate rodent responses to spaceflight in low-Earth orbit. Here we have confirmed the expression of these proposed spaceflight associated miRNAs in rodents reacting to simulated spaceflight conditions (exposure to ionizing radiation combined with simulated microgravity) and in astronaut samples from the NASA Twins Study via direct quantification of miRNAs, miRNA sequencing, and inferring miRNA target levels based on single-cell RNA (scRNA-seq) and single-cell chromatin (scATAC-seq) sequencing data. To demonstrate the physiological relevance of key spaceflight associated miRNAs, we utilized antagomirs to inhibit their expression and successfully rescue simulated deep space radiation-mediated damage in human 3D vascular constructs.

Subjects

Subjects :
Aerospace Medicine

Details

Language :
English
Database :
NASA Technical Reports
Notes :
NNX16AO69A
Publication Type :
Report
Accession number :
edsnas.20205008847
Document Type :
Report