Circulating miRNA Spaceflight Signature Reveals Targets for Countermeasure Development.

Sherina Malkani, Christopher R Chin,Egle Cekanaviciute, Marie Mortreux, Hazeem Okinula,Marcel Tarbier,Ann-Sofie Schreurs, Yasaman Shirazi-Fard,Candice G T 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,Ebrahim Afshinnekoo,Brad W Langhorst, Eileen T Dimalanta,Margareth Cheng-Campbell, Elizabeth Blaber,Jonathan C Schisler,Charles Vanderburg, Marc R Friedländer,J Tyson McDonald, Sylvain V Costes,Seward Rutkove, Peter Grabham,Christopher E Mason,Afshin Beheshti

Cell reports(2020)

引用 32|浏览74
暂无评分
摘要
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.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要