PUBLICATION
Pathway analysis of systemic transcriptome responses to injected polystyrene particles in zebrafish larvae
- Authors
- Veneman, W.J., Spaink, H.P., Brun, N.R., Bosker, T., Vijver, M.G.
- ID
- ZDB-PUB-170714-2
- Date
- 2017
- Source
- Aquatic toxicology (Amsterdam, Netherlands) 190: 112-120 (Journal)
- Registered Authors
- Spaink, Herman P.
- Keywords
- Adverse outcome pathway, Key event, Microplastic, RNA sequencing, Zebrafish embryo
- Datasets
- GEO:GSE77755
- MeSH Terms
-
- Animals
- Gene Expression Profiling
- Larva/genetics
- Larva/metabolism
- Particle Size
- Polystyrenes/pharmacokinetics
- Polystyrenes/toxicity*
- Tissue Distribution
- Transcriptome/drug effects*
- Water Pollutants, Chemical/pharmacokinetics
- Water Pollutants, Chemical/toxicity*
- Zebrafish/genetics
- Zebrafish/metabolism*
- PubMed
- 28704660 Full text @ Aquat. Toxicol.
Citation
Veneman, W.J., Spaink, H.P., Brun, N.R., Bosker, T., Vijver, M.G. (2017) Pathway analysis of systemic transcriptome responses to injected polystyrene particles in zebrafish larvae. Aquatic toxicology (Amsterdam, Netherlands). 190:112-120.
Abstract
Microplastics are a contaminant of emergent concern in the environment, however, to date there is a limited understanding on their movement within organisms and the response of organisms. In the current study zebrafish embryos at different development stages were exposed to 700nm fluorescent polystyrene (PS) particles and the response pathway after exposure was investigated using imaging and transcriptomics. Our results show limited spreading of particles within the larvae after injection during the blastula stage. This is in contrast to injection of PS particles in the yolk of 2-day old embryos, which resulted in redistribution of the PS particles throughout the bloodstream, and accumulation in the heart region. Although injection was local, the transcriptome profiling showed strong responses of zebrafish embryos exposed to PS particle, indicating a systemic response. We found several biological pathways activated which are related to an immune response in the PS exposed zebrafish larvae. Most notably the complement system was enriched as indicated by upregulation of genes in the alternative complement pathway (e.g. cfhl3, cfhl4, cfb and c9). The fact that complement pathway is activated indicates that plastic microparticles are integrated in immunological recognition processes. This was supported by fluorescence microscopy results, in which we observed co-localisation of neutrophils and macrophages around the PS particles. Identifying these key events can be a first building block to the development of an adverse outcome pathway (AOP). These data subsequently can be used within ecological and human risk assessment.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping