作者
Sherina Malkani,Christopher R. Chin,Egle Cekanaviciute,Marie Mortreux,Hazeem Okinula,Marcel Tarbier,Ann‐Sofie Schreurs,Yasaman Shirazi‐Fard,Candice Tahimic,Deyra N. Rodríguez,Brittany S. Sexton,Daniel Butler,Akanksha Verma,Daniela Bezdan,Ceyda Durmaz,Matthew MacKay,Ari Melnick,Cem Meydan,Sheng Li,Francine E. Garrett-Bakelman,Bastian Fromm,Ebrahim Afshinnekoo,Bradley W. Langhorst,Eileen T. Dimalanta,Margareth Cheng-Campbell,Elizabeth A. Blaber,Jonathan C. Schisler,Charles Vanderburg,Marc R. Friedländer,J. Tyson McDonald,Sylvain V. Costes,Seward B. Rutkove,Peter Grabham,Christopher E. Mason,Afshin Beheshti
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.