A systems biology approach reveals neuronal and muscle developmental defects after chronic exposure to ionising radiation in zebrafish.
Sophia Murat El HoudiguiChristelle Adam-GuillerminGiovanna LoroCaroline ArcanjoSandrine FrelonMagali FlorianiNicolas DubourgEmilie BaudeletStéphane AudebertLuc CamoinOlivier ArmantPublished in: Scientific reports (2019)
Contamination of the environment after the Chernobyl and Fukushima Daiichi nuclear power plant (NPP) disasters led to the exposure of a large number of humans and wild animals to radioactive substances. However, the sub-lethal consequences induced by these absorbed radiological doses remain understudied and the long-term biological impacts largely unknown. We assessed the biological effects of chronic exposure to ionizing radiation (IR) on embryonic development by exposing zebrafish embryo from fertilization and up to 120 hours post-fertilization (hpf) at dose rates of 0.5 mGy/h, 5 mGy/h and 50 mGy/h, thereby encompassing the field of low dose rates defined at 6 mGy/h. Chronic exposure to IR altered larval behaviour in a light-dark locomotor test and affected cardiac activity at a dose rate as low as 0.5 mGy/h. The multi-omics analysis of transcriptome, proteome and transcription factor binding sites in the promoters of the deregulated genes, collectively points towards perturbations of neurogenesis, muscle development, and retinoic acid (RA) signaling after chronic exposure to IR. Whole-mount RNA in situ hybridization confirmed the impaired expression of the transcription factors her4.4 in the central nervous system and myogenin in the developing muscles of exposed embryos. At the organ level, the assessment of muscle histology by transmission electron microscopy (TEM) demonstrated myofibers disruption and altered neuromuscular junctions in exposed larvae at 5 mGy/h and 50 mGy/h. The integration of these multi-level data demonstrates that chronic exposure to low dose rates of IR has an impact on neuronal and muscle progenitor cells, that could lead to motility defects in free swimming larvae at 120 hpf. The mechanistic understanding of these effects allows us to propose a model where deregulation of RA signaling by chronic exposure to IR has pleiotropic effects on neurogenesis and muscle development.
Keyphrases
- low dose
- transcription factor
- skeletal muscle
- rheumatoid arthritis
- risk assessment
- gene expression
- machine learning
- high dose
- cerebral ischemia
- staphylococcus aureus
- radiation therapy
- zika virus
- escherichia coli
- disease activity
- genome wide
- ankylosing spondylitis
- single molecule
- climate change
- systemic lupus erythematosus
- heavy metals
- left ventricular
- long non coding rna
- single cell
- electron microscopy
- interstitial lung disease
- atrial fibrillation
- big data
- cerebrospinal fluid
- neural stem cells