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Circulating miRNA Spaceflight Signature Reveals Targets for Countermeasure Development

机译:循环miRNA航天签名揭示了对策发展的目标

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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.
机译:我们已经确定并验证了啮齿动物和人类共享的空间相关的MicroRNA(miRNA)签名,以应对模拟,短持续时间和长期空光。以前的研究已经确定了MIRNA,其调节对低地轨道中的空间的啮齿动物反应,并且我们已经证实了这些提出的空气相关的MIRNA在对模拟的空间环境反应的啮齿动物中的表达。此外,来自NASA双胞胎研究的宇航员样品证实了MiRNA测序,单细胞RNA测序(ScRNA-SEQ)中的这些表达鉴定,以及用于转座酶可接受的染色质(SCATAC-SEQ)数据的单细胞测定。另外,发现这些miRNA(miR-125,miR-16和Let-7a)的子集来调节由模拟的深空辐射引起的血管损伤。为了证明关键空云相关的miRNA的生理相关性,我们利用抗宫抑制它们的表达,并成功拯救了人3D血管构建体中的模拟深空辐射损伤。
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