Cerium Oxide Nanoparticle Administration to Skeletal Muscle Cells under Different Gravity and Radiation Conditions.
Giada Graziana GenchiAndrea Degl'InnocentiChiara MartinelliMatteo BattagliniDaniele De PasqualeMirko PratoSergio MarrasGiammarino PuglieseFilippo DragoAlessandro MarianiMichele BalsamoValfredo ZolesiGianni CiofaniPublished in: ACS applied materials & interfaces (2021)
For their remarkable biomimetic properties implying strong modulation of the intracellular and extracellular redox state, cerium oxide nanoparticles (also termed "nanoceria") were hypothesized to exert a protective role against oxidative stress associated with the harsh environmental conditions of spaceflight, characterized by microgravity and highly energetic radiations. Nanoparticles were supplied to proliferating C2C12 mouse skeletal muscle cells under different gravity and radiation levels. Biological responses were thus investigated at a transcriptional level by RNA next-generation sequencing. Lists of differentially expressed genes (DEGs) were generated and intersected by taking into consideration relevant comparisons, which led to the observation of prevailing effects of the space environment over those induced by nanoceria. In space, upregulation of transcription was slightly preponderant over downregulation, implying involvement of intracellular compartments, with the majority of DEGs consistently over- or under-expressed whenever present. Cosmic radiations regulated a higher number of DEGs than microgravity and seemed to promote increased cellular catabolism. By taking into consideration space physical stressors alone, microgravity and cosmic radiations appeared to have opposite effects at transcriptional levels despite partial sharing of molecular pathways. Interestingly, gene ontology denoted some enrichment in terms related to vision, when only effects of radiations were assessed. The transcriptional regulation of mitochondrial uncoupling protein 2 in space-relevant samples suggests perturbation of the intracellular redox homeostasis, and leaves open opportunities for antioxidant treatment for oxidative stress reduction in harsh environments.
Keyphrases
- oxidative stress
- induced apoptosis
- oxide nanoparticles
- skeletal muscle
- transcription factor
- signaling pathway
- cell cycle arrest
- endoplasmic reticulum stress
- insulin resistance
- diabetic rats
- genome wide
- dna damage
- gene expression
- ischemia reperfusion injury
- reactive oxygen species
- cell proliferation
- copy number
- heat shock
- cell death
- social media
- genome wide identification
- physical activity
- nitric oxide
- poor prognosis
- radiation therapy
- single molecule
- radiation induced
- human health
- dna methylation
- health information
- metabolic syndrome
- mass spectrometry
- combination therapy
- adipose tissue
- heat stress
- atomic force microscopy
- electron transfer
- amino acid
- pi k akt
- circulating tumor