Spatially resolved multiomics on the neuronal effects induced by spaceflight in mice.
Yuvarani MasarapuEgle CekanaviciuteZaneta AndrusivovaJakub Orzechowski WestholmÅsa K BjörklundRobin FalleggerPau Badia-I-MompelValery BoykoShubha VasishtAmanda Saravia-ButlerSamrawit GebreEnikő LázárMarta GrazianoSolène FrapardRobert G HinshawOlaf BergmannDeanne M TaylorDouglas C WallaceChrister SylvénKonstantinos MeletisJulio Saez-RodriguezJonathan M GalazkaSylvain V CostesStefania GiacomelloPublished in: Nature communications (2024)
Impairment of the central nervous system (CNS) poses a significant health risk for astronauts during long-duration space missions. In this study, we employed an innovative approach by integrating single-cell multiomics (transcriptomics and chromatin accessibility) with spatial transcriptomics to elucidate the impact of spaceflight on the mouse brain in female mice. Our comparative analysis between ground control and spaceflight-exposed animals revealed significant alterations in essential brain processes including neurogenesis, synaptogenesis and synaptic transmission, particularly affecting the cortex, hippocampus, striatum and neuroendocrine structures. Additionally, we observed astrocyte activation and signs of immune dysfunction. At the pathway level, some spaceflight-induced changes in the brain exhibit similarities with neurodegenerative disorders, marked by oxidative stress and protein misfolding. Our integrated spatial multiomics approach serves as a stepping stone towards understanding spaceflight-induced CNS impairments at the level of individual brain regions and cell types, and provides a basis for comparison in future spaceflight studies. For broader scientific impact, all datasets from this study are available through an interactive data portal, as well as the National Aeronautics and Space Administration (NASA) Open Science Data Repository (OSDR).
Keyphrases
- single cell
- rna seq
- cerebral ischemia
- oxidative stress
- resting state
- health risk
- functional connectivity
- white matter
- blood brain barrier
- high throughput
- dna damage
- electronic health record
- big data
- public health
- heavy metals
- diabetic rats
- type diabetes
- stem cells
- ischemia reperfusion injury
- skeletal muscle
- high glucose
- brain injury
- cerebrospinal fluid
- quality improvement
- dna methylation
- metabolic syndrome
- prefrontal cortex
- endothelial cells
- drinking water
- deep learning
- mesenchymal stem cells
- cognitive impairment
- induced apoptosis