4.8 Article

Circulating miRNA Spaceflight Signature Reveals Targets for Countermeasure Development

期刊

CELL REPORTS
卷 33, 期 10, 页码 -

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2020.108448

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资金

  1. STARR [I13-0052]
  2. NASA [NNX14AH50G, NNX17AB26G, 19-19OMNI_2-0109, 16-ROSBFP_GL-0005: NNH16ZTT001N-FG, 80NSSC19K0883, NNX16AO69A(T-0404)]
  3. National Institutes for Health [R01MH117406, R01CA249054, LLS-MCL7001-18, NNX16AO69A:0107, NNX16AO69A:0061, LLS 9238-16]
  4. International Space Station U.S. National Laboratory [UA-2019-018]

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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.

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