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Circulating miRNA Spaceflight Signature Reveals Targets for Countermeasure Development.
- Source :
-
Cell reports [Cell Rep] 2020 Dec 08; Vol. 33 (10), pp. 108448. Date of Electronic Publication: 2020 Nov 25. - Publication Year :
- 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. Previous studies have identified miRNAs that regulate rodent responses to spaceflight in low-Earth orbit, and we have confirmed the expression of these proposed spaceflight-associated miRNAs in rodents reacting to simulated spaceflight conditions. Moreover, astronaut samples from the NASA Twins Study confirmed these expression signatures in miRNA sequencing, single-cell RNA sequencing (scRNA-seq), and single-cell assay for transposase accessible chromatin (scATAC-seq) data. Additionally, a subset of these miRNAs (miR-125, miR-16, and let-7a) was found to regulate vascular damage caused by simulated deep space radiation. 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.<br />Competing Interests: Declaration of Interests The authors declare no competing interests.<br /> (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Female
Gene Expression
Gene Expression Profiling methods
Humans
Male
Mice
Mice, Inbred BALB C
Middle Aged
Rats
Sequence Analysis, RNA methods
Space Flight
Transcriptome genetics
Weightlessness Simulation methods
Circulating MicroRNA genetics
MicroRNAs genetics
Weightlessness adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 33
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 33242410
- Full Text :
- https://doi.org/10.1016/j.celrep.2020.108448