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
- health risk
- resting state
- white matter
- functional connectivity
- blood brain barrier
- dna damage
- diabetic rats
- electronic health record
- gene expression
- stem cells
- drinking water
- public health
- type diabetes
- big data
- high fat diet induced
- transcription factor
- mass spectrometry
- metabolic syndrome
- genome wide
- mesenchymal stem cells
- subarachnoid hemorrhage
- skeletal muscle
- dna methylation
- adipose tissue
- neural stem cells
- brain injury
- current status
- ischemia reperfusion injury
- heat shock protein
- amino acid
- data analysis