PUBLICATION

Single-cell RNA sequencing reveals size-dependent effects of polystyrene microplastics on immune and secretory cell populations from zebrafish intestines

Authors
Gu, W., Liu, S., Chen, L., Liu, Y., Gu, C., Ren, H.Q., Wu, B.
ID
ZDB-PUB-200225-43
Date
2020
Source
Environmental science & technology   54(6): 3417-3427 (Journal)
Registered Authors
Keywords
none
Datasets
GEO:GSE136108, GEO:GSE135767, GEO:GSE136109
MeSH Terms
  • Animals
  • Intestines
  • Microplastics
  • Plastics
  • Polystyrenes*
  • Sequence Analysis, RNA
  • Zebrafish*
PubMed
32092251 Full text @ Env. Sci. Tech.
Abstract
Microplastics (MPs) as widespread contamination pose a high risk for aquatic organisms. However, current understanding of MP toxicity is based on cell population-averaged measurements. Our aim was to gain a comprehensive understanding of the size-dependent effects of polystyrene MPs (PS-MPs) on intestinal cell populations in zebrafish and characterize the interplay of MPs, intestinal cells and intestinal microbiota. Here, we used single-cell RNA sequencing to determine the transcriptome heterogeneity of 12000 intestinal cells obtained from zebrafish exposed to 100-nm, 5-μm and 200-μm PS-MPs for 21 days. Eight intestinal cell populations were identified. Combined with changes in intestinal microbiota, our findings highlight a previously unrecognized endpoint that all three sizes of PS-MPs induced dysfunction of intestinal immune cells (including effects on phagosomes and regulation of immune system processes) and increased the abundance of pathogenic bacteria. However, only 100-nm PS-MPs altered expression of genes related to phagocyte-produced ROS generation and increased mucus secretion by secretory cells. Microsize PS-MPs specifically changed the lysosome (5 μm) and cell surface receptor signaling (200 μm) processes of macrophages. Our findings pinpoint to cell-specific and size-dependent responses to PS-MPs in fish intestine, which can provide a reference for future study directions.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping